Professor Joel Tyndall

2026

Journal - Research Article

Roohi, B., Tyndall, J. D. A., Svoboda, T., de Hoog, S., Crous, P. W., Monk, B. C., … Lackner, M. (2026). The dual role of azoles: Lifesaving antifungals and drivers of resistance: A One Health perspective. Nature Communications. Advance online publication. doi: 10.1038/s41467-026-71762-9

Belcher, C. M., Souza, C. P., McGuire, E., Hung, C.-C., Tyndall, J. D. A., & Hoyer, L. L. (2026). Phylogenetic and structural analysis of miconazole susceptibility in Malassezia pachydermatis isolates from dogs with otitis externa. Veterinary Determatology. Advance online publication. doi: 10.1111/vde.70059

Zhao, M., Niimi, M., Niimi, K., Chindamporn, A., Kajiwara, S., Bonus, M., … Tyndall, J. D. A., Cannon, R. D., & Lamping, E. (2026). G521 is the gatekeeper and a key transmembrane domain contact residue of Candida albicans Cdr1. mBio. Advance online publication. doi: 10.1128/mbio.03746-25

2025

Journal - Research Article

Fleming, C., Nugent, H., Loli Quinteros, S., Fernando, B. S. M., Tyndall, J. D. A., Webb, J. K., … Huston, W. M. (2025). A pilot study of re-purposing drugs to treat koalas with chlamydia. Scientific Reports. Advance online publication. doi: 10.1038/s41598-025-29789-3

Alsulaimany, M., Keniya, M. V., Alanazi, R. S., Ruma, Y. N., Hughes, C. S., Jones, A. T., Tyndall, J. D. A., … Monk, B. C., & Simons, C. (2025). Exploring long arm amide-linked side chains in the design of antifungal azole inhibitors of sterol 14α-demethylase (CYP51). Journal of Medicinal Chemistry. Advance online publication. doi: 10.1021/acs.jmedchem.4c02922

Edupuganti, V. V. S. R., Matikonda, S. S., Lawer, A., Fairhall, J. M., Lewin, H. M., Kueh, J. T. B., Tyndall, J. D. A., & Gamble, A. B. (2025). Stimuli-responsive prodrug linkers that simultaneously release cargo and neutralize in situ generate (aza)quinone methides. Chemistry: A European Journal, e202501278. Advance online publication. doi: 10.1002/chem.202501278

2024

Journal - Research Article

Hosseini, P., Keniya, M. V., Sagatova, A. A., Toepfer, S., Müller, C., Tyndall, J. D. A., … Monk, B. C. (2024). The molecular basis of the intrinsic and acquired resistance to azole antifungals in Aspergillus fumigatus. Journal of Fungi, 10, 820. doi: 10.3390/jof10120820

Putha, L., Kok, L. K., Fellner, M., Rutledge, M. T., Gamble, A. B., Wilbanks, S. M., Vernall, A. J., & Tyndall, J. D. A. (2024). Covalent isothiocyanate inhibitors of macrophage migration inhibitory factor as potential colorectal cancer treatments. ChemMedChem, 19, e202400394. doi: 10.1002/cmdc.202400394

Chao, Y., Wang, R., Ni, T., Monk, B. C., Tyndall, J. D. A., Bao, J., … Xie, F. (2024). Synthesis and antifungal evaluation of novel triazole derivatives bearing a pyrazole-methoxyl moiety. European Journal of Medicinal Chemistry, 275, 116637. doi: 10.1016/j.ejmech.2024.116637

Payne, C. M., Baltos, J.-A., Langiu, M., Lu, C. S., Tyndall, J. D. A., Gregory, K. J., … Vernall, A. J. (2024). Development of putative bivalent dicovalent ligands for the adenosine A1 receptor. ChemBioChem, 25, e202400242. doi: 10.1002/cbic.202400242

Adolph, C., Cheung, C.-Y., McNeil, M. B., Jowsey, W. J., Williams, Z. C., Hards, K., Harold, L. K., … Tyndall, J. D. A., … Cook, G. M. (2024). A dual-targeting succinate dehydrogenase and F₁F_o-ATP synthase inhibitor rapidly sterilizes replicating and non-replicating Mycobacterium tuberculosis. Cell Chemical Biology, 31(4), 683-698. doi: 10.1016/j.chembiol.2023.12.002

Conference Contribution - Published proceedings: Abstract

Tyler, C., Lawer, A., Tyndall, J. D. A., Cook, G. M., & Gamble, A. B. (2024). Synthesis and biological evaluation of antitubercular inhibitors. Proceedings of the New Zealand Institute of Chemistry (NZIC) Conference. (pp. 161). Retrieved from https://nzic.org.nz/conferences

Tyndall, J. D. A., Putha, L., Kok, L. K., Fellner, M., Rutledge, M. T., Gamble, A. B., Wilbanks, S. M., & Vernall, A. J. (2024). Covalent inhibition of macrophage migration inhibitory factor by isothiocyanates as potential colorectal cancer leads. Proceedings of the New Zealand Institute of Chemistry (NZIC) Conference. (pp. 67). Retrieved from https://nzic.org.nz/conferences

Gilmer, S. C. L., Tyndall, J. D. A., & Vernall, A. J. (2024). Development of bifunctional chemical tools for the adenosine A₁ Receptor. Proceedings of the New Zealand Institute of Chemistry (NZIC) Conference. (pp. 51). Retrieved from https://nzic.org.nz/conferences

Conference Contribution - Verbal presentation and other Conference outputs

Tyler, C., Lawer, A., Tyndall, J. D. A., Cook, G. M., & Gamble, A. B. (2024, November). Design and evaluation of antituberculosis molecules. Verbal presentation at the School of Pharmacy Research Symposium, Dunedin, New Zealand.

Liddle, I., de la Harpe, S., Rajapakse, C., Glass, M., Tyndall, J., & Vernall, A. (2024, November). Allosteric modulators for the cannabinoid receptor 2. Verbal presentation at the School of Pharmacy Research Symposium, Dunedin, New Zealand.

Tyndall, J. D. A., Putha, L., Kok, L. K., Fellner, M., Rutledge, M. T., Gamble, A. B., Wilbanks, S. M., & Vernall, A. J. (2024, November). Covalent MIF inhibitors as anticancer leads. Verbal presentation at the School of Pharmacy Research Symposium, Dunedin, New Zealand.

2023

Chapter in Book - Research

Payne, C., Awalt, J. K., May, L. T., Tyndall, J. D. A., Jörg, M., & Vernall, A. J. (2023). Bifunctional tools to study adenosine receptors. In V. Colotta & C. T. Supuran (Eds.), Purinergic receptors and their modulators. (pp. 179-221). Cham, Switzerland: Springer. doi: 10.1007/7355_2022_154

Journal - Research Article

Yin, J., Sharma, R., Tyndall, J. D. A., Grimsey, N. L., & Vernall, A. J. (2023). Synthesis and characterization of a cannabinoid type 2 receptor photoactivated prodrug. ChemPhotoChem, 7, e202200291. doi: 10.1002/cptc.202200291

Conference Contribution - Published proceedings: Abstract

Tyler, C., Lawer, A., Tyndall, J. D. A., Cook, G. M., & Gamble, A. (2023). Design and synthesis of novel antitubercular inhibitors. Proceedings of the New Zealand Controlled Release Society (NZCRS) Symposium. Retrieved from http://nzcrs.org.nz/#/home

Other Research Output

Tyndall, J. (2023, September). Targeting HtrA protease: Systematic modification to potential new antibacterial leads. Department of Microbiology and Immunology Seminar, University of Otago, Dunedin, New Zealand. [Department Seminar].

Tyndall, J. (2023, July). Looking at molecules and what they do in disease. University of Otago, Dunedin, New Zealand. [Inaugural Professorial Lecture].

2022

Journal - Research Article

Lawer, A., Tyler, C., Hards, K., Keighley, L. M., Cheung, C.-Y., Kierek, F., Su, S., … McInnes, T., Tyndall, J. D. A., Krause, K. L., Cook, G. M., & Gamble, A. B. (2022). Synthesis and biological evaluation of aurachin D analogues as inhibitors of Mycobacterium tuberculosis cytochrome bd oxidase. ACS Medicinal Chemistry Letters, 13, 1663-1669. doi: 10.1021/acsmedchemlett.2c00401

Hards, K., Cheung, C.-Y., Waller, N., Adolph, C., Keighley, L., Tee, Z. S., Harold, L. K., Menorca, A., … Tyndall, J. D. A., McNeil, M. B., … Opel-Reading, H. K., Krause, K. L., … Berney, M., … Cook, G. M. (2022). An amiloride derivative is active against the F₁F_o-ATP synthase and cytochrome bd oxidase of Mycobacterium tuberculosis. Communications Biology, 5, 166. doi: 10.1038/s42003-022-03110-8

Hwang, J., Mros, S., Gamble, A. B., Tyndall, J. D. A., & McDowell, A. (2022). Improving antibacterial activity of a HtrA protease inhibitor JO146 against Helicobacter pylori: A novel approach using microfluidics-engineered PLGA nanoparticles. Pharmaceutics, 14(2), 348. doi: 10.3390/pharmaceutics14020348

McNeil, N. M. R., Gates, E. W. J., Firoozi, N., Cundy, N. J., Leccese, J., Eisinga, S., Tyndall, J. D. A., … Keillor, J. W. (2022). Structure-activity relationships of N-terminal variants of peptidomimetic tissue transglutaminase inhibitors. European Journal of Medicinal Chemistry, 232, 114172. doi: 10.1016/j.ejmech.2022.114172

Ruma, Y. N., Keniya, M. V., Tyndall, J. D. A., & Monk, B. C. (2022). Characterisation of Candida parapsilosis CYP51 as a drug target using Saccharomyces cerevisiae as host. Journal of Fungi, 8(1), 69. doi: 10.3390/jof8010069

Hwang, J., Strange, N., Mazraani, R., Phillips, M. J., Gamble, A. B., Huston, W. M., & Tyndall, J. D. A. (2022). Design, synthesis and biological evaluation of P2-modified proline analogues targeting the HtrA serine protease in Chlamydia. European Journal of Medicinal Chemistry. doi: 10.1016/j.ejmech.2021.114064

Journal - Research Other

Tyndall, J. D. A. (2022). S-217622, a 3CL protease inhibitor and clinical candidate for SARS-CoV-2. Journal of Medicinal Chemistry, 65, 6496-6498. doi: 10.1021/acs.jmedchem.2c00624

Liddle, I., Glass, M., Tyndall, J. D. A., & Vernall, A. J. (2022). Covalent cannabinoid receptor ligands: Structural insight and selectivity challenges. RSC Medicinal Chemistry, 13, 497-510. doi: 10.1039/D2MD00006G

Conference Contribution - Published proceedings: Abstract

Liddle, I., Glass, M., Tyndall, J. D. A., & Vernall, A. J. (2022). Covalent chromenopyrazole chemical tools for the cannabinoid type 2 receptor. In L. Wilson, H. Harcombe, P. Jayakaran, L. Burga, J. Antony, K. Morgaine, M. Garelja, A. Middleton, M. Anwar & T. Milne (Eds.), Proceedings of the 263rd Otago Medical School Research Society (OMSRS) Meeting: PhD Student Speaker Awards. Dunedin, New Zealand: OMSRS. Retrieved from https://ourarchive.otago.ac.nz/handle/10523/12839

Conference Contribution - Verbal presentation and other Conference outputs

Rana, Z., Tyndall, J. D. A., Diermeier, S., Hanif, M., & Rosengren, R. J. (2022, August). Cytostatic role of safe novel HDAC inhibitors in AR- prostate cancer. Verbal presentation at the Cancer Satellite Meeting: Queenstown Research Week, Queenstown, New Zealand.

2021

Journal - Research Article

Graham, D. O., Wilson, R. K., Ruma, Y. N., Keniya, M. V., Tyndall, J. D. A., & Monk, B. C. (2021). Structural insights into the azole resistance of the Candida albicans Darlington strain using Saccharomyces cerevisiae lanosterol 14α-demethylase as a surrogate. Journal of Fungi, 7, 897. doi: 10.3390/jof7110897

McDougall, L., Kueh, J. T. B., Ward, J., Tyndall, J. D. A., Woolley, A. G., Mehta, S., Stayner, C., Larsen, D. S., & Eccles, M. R. (2021). Chemical synthesis of the PAX protein inhibitor EG1 and its ability to slow the growth of human colorectal carcinoma cells. Frontiers in Oncology, 11, 709540. doi: 10.3389/fonc.2021.709540

Hwang, J., Strange, N., Phillips, M. J. A., Krause, A. L., Heywood, A., Gamble, A. B., … Tyndall, J. D. A. (2021). Optimization of peptide-based inhibitors targeting the HtrA serine protease in Chlamydia: Design, synthesis and biological evaluation of pyridone-based and N-Capping group-modified analogues. European Journal of Medicinal Chemistry, 224(113692). doi: 10.1016/j.ejmech.2021.113692

Trinh, P. N. H., Chong, D. J. W., Leach, K., Hill, S. J., Tyndall, J. D. A., May, L. T., Vernall, A. J., & Gregory, K. J. (2021). Development of covalent, clickable probes for adenosine A₁ and A₃ receptors. Journal of Medicinal Chemistry, 64, 8161-8178. doi: 10.1021/acs.jmedchem.0c02169

Murugayah, S. A., Evans, G. B., Tyndall, J. D. A., & Gerth, M. L. (2021). A single point mutation converts a glutaryl-7-aminocephalosporanic acid acylase into an N-acyl-homoserine lactone acylase. Biotechnology Letters, 43, 1467-1473. doi: 10.1007/s10529-021-03135-9

Wen, Y., Cai, W., Yang, J., Fu, X., Putha, L., Xia, Q., … Tyndall, J. D. A., … Huang, W. (2021). Targeting macrophage migration inhibitory factor in acute pancreatitis and pancreatic cancer. Frontiers in Pharmacology, 12, 638950. doi: 10.3389/fphar.2021.638950

Liang, G., Yang, J., Liu, T., Wang, S., Wen, Y., Han, C., … Tyndall, J. D. A., … Xia, Q. (2021). A multi-strategy platform for quality control and Q-markers screen of Chaiqin chengqi decoction. Phytomedicine, 85, 153525. doi: 10.1016/j.phymed.2021.153525

Rana, Z., Tyndall, J. D. A., Hanif, M., Hartinger, C. G., & Rosengren, R. J. (2021). Cytostatic action of novel histone deacetylase inhibitors in androgen receptor-null prostate cancer cells. Pharmaceuticals, 14, 103. doi: 10.3390/ph14020103

Singh, S., Liddle, I., Macdonald, C., Tyndall, J. D. A., Glass, M., & Vernall, A. (2021). Development of chromenopyrazole-based selective cannabinoid 2 receptor agonists. Australian Journal of Chemistry, 74, 433-442. doi: 10.1071/CH20263

Journal - Research Other

Edupuganti, V. V. S. R., Tyndall, J. D. A., & Gamble, A. B. (2021). Self-immolative linkers in prodrugs and antibody drug conjugates in cancer treatment. Recent Patents on Anti-Cancer Drug Discovery, 16(4), 479-497. doi: 10.2174/1574892816666210509001139

2020

Journal - Research Article

Handley, T. N. G., Tan, H.-X., Rutledge, M. T., Brewitz, H. H., Tyndall, J. D. A., Kleffmann, T., Butler, M. I., Poulter, R. T. M., & Wilbanks, S. M. (2020). Engineered biosynthesis of cyclotides. New Zealand Journal of Botany, 58(4), 358-377. doi: 10.1080/0028825X.2020.1791914

Schneider, M., Hannaway, R. F., Lamichhane, R., de la Harpe, S. M., Tyndall, J. D. A., Vernall, A. J., Kettle, A. J., & Ussher, J. E. (2020). Neutrophils suppress mucosal-associated invariant T cells in humans. European Journal of Immunology, 50, 643-655. doi: 10.1002/eji.201948394

Lamichhane, R., Galvin, H., Hannaway, R. F., de la Harpe, S. M., Munro, F., Tyndall, J. D. A., Vernall, A. J., McCall, J. L., Husain, M., & Ussher, J. E. (2020). Type I interferons are important co-stimulatory signals during T cell receptor mediated human MAIT cell activation. European Journal of Immunology, 50, 178-191. doi: 10.1002/eji.201948279

2019

Journal - Research Article

Lamichhane, R., Schneider, M., de la Harpe, S. M., Harrop, T. W. R., Hannaway, R. F., Dearden, P. K., Kirman, J. R., Tyndall, J. D. A., Vernall, A. J., & Ussher, J. E. (2019). TCR- or cytokine-activated CD8⁺ mucosal-associated invariant T cells are rapid polyfunctional effectors that can coordinate immune responses. Cell Reports, 28(12), 3061-3076.e5. doi: 10.1016/j.celrep.2019.08.054

Agbowuro, A. A., Hwang, J., Peel, E., Mazraani, R., Springwald, A., Marsh, J. W., … Gamble, A. B., … Tyndall, J. D. A. (2019). Structure-activity analysis of peptidic Chlamydia HtrA inhibitors. Bioorganic & Medicinal Chemistry, 27, 4185-4199. doi: 10.1016/j.bmc.2019.07.049

Monk, B. C., Keniya, M. V., Sabherwal, M., Wilson, R. K., Graham, D. O., Hassan, H. F., Chen, D., & Tyndall, J. D. A. (2019). Azole resistance reduces susceptibility to the tetrazole antifungal VT-1161. Antimicrobial Agents & Chemotherapy, 63(1), e02114-18. doi: 10.1128/AAC.02114-18

Conference Contribution - Published proceedings: Abstract

Hosseini, P., Keniya, M. V., Tyndall, J. D. A., & Monk, B. C. (2019). Functional expression of Aspergillus fumigatus CYP51 isoforms in Saccharomyces cerevisiae. Proceedings of the New Zealand Microbiological Society (NZMS) Annual Conference. 666. Retrieved from https://www.nzmscoference.org.nz

Monk, B. C., Lackner, M., Tyndall, J. D. A., & Keniya, M. V. (2019). Amino acid substitutions in lanosterol 14α-demethylase responsible for intrinsic azole resistance in mucormycetes. Proceedings of the New Zealand Microbiological Society (NZMS) Annual Conference. 571. Retrieved from https://www.nzmscoference.org.nz

Ruma, Y. N., Keniya, M. V., Tyndall, J. D. A., & Monk, B. C. (2019). Characterization of Cryptococcus neoformans lanosterol 14α-demethylase. New Zealand Dental Journal, 115, (pp. 167). [Abstract]

Conference Contribution - Verbal presentation and other Conference outputs

Monk, B. C., Sagatova, A. A., Wilson, R. K., Tyndall, J. D. A., Lackner, M., Ruma, Y. N., Hosseini, P., & Keniya, M. V. (2019, August-September). Drug discovery using the antifungal target lanosterol 14α-demethylase. Verbal presentation at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

Singh, S., Oyagawa, C. R. M., Grimsey, N. L., Tyndall, J. D. A., Glass, M., & Vernall, A. J. (2019, August-September). Chromenopyrazole-based chemical tools to study cannabinoid type 2 receptor. Verbal presentation at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

2018

Journal - Research Article

Cooper, A. G., Oyagawa, C. R. M., Manning, J. J., Singh, S., Hook, S., Grimsey, N. L., Glass, M., Tyndall, J. D. A., & Vernall, A. J. (2018). Development of selective, fluorescent cannabinoid type 2 receptor ligands based on a 1,8-naphthyridin-2-(1H)-one-3-carboxamide scaffold. MedChemComm, 9(12), 2055-2067. doi: 10.1039/c8md00448j

Keniya, M. V., Ruma, Y. N., Tyndall, J. D. A., & Monk, B. C. (2018). Heterologous expression of full-length lanosterol 14α-demethylases of prominent fungal pathogens Candida albicans and Candida glabrata provides tools for antifungal discovery. Antimicrobial Agents & Chemotherapy, 62(11), e01131-18. doi: 10.1128/aac.01131-18

Keniya, M. V., Sabherwal, M., Wilson, R. K., Woods, M. A., Sagatova, A. A., Tyndall, J. D. A., & Monk, B. C. (2018). Crystal structures of full-length lanosterol 14α-demethylases of prominent fungal pathogens Candida albicans and Candida glabrata provide tools for antifungal discovery. Antimicrobial Agents & Chemotherapy, 62(11), e01134-18. doi: 10.1128/aac.01134-18

Singh, S., Cooper, S. L., Glenn, J. R., Beresford, J., Percival, L. R., Tyndall, J. D. A., … Vernall, A. J. (2018). Synthesis of novel (benzimidazolyl)isoquinolinols and evaluation as adenosine A1 receptor tools. RSC Advances, 8(29), 16362-16369. doi: 10.1039/C7RA13148H

Sagatova, A. A., Keniya, M. V., Tyndall, J. D. A., & Monk, B. C. (2018). The impact of homologous resistance mutations from pathogenic yeast on Saccharomyces cerevisiae lanosterol 14α-demethylase. Antimicrobial Agents & Chemotherapy, 62(3), e02242-17. doi: 10.1128/aac.02242-17

Cooper, A. G., MacDonald, C., Glass, M., Hook, S., Tyndall, J. D. A., & Vernall, A. J. (2018). Alkyl indole-based cannabinoid type 2 receptor tools: Exploration of linker and fluorophore attachment. European Journal of Medicinal Chemistry, 145, 770-789. doi: 10.1016/j.ejmech.2017.11.076

Agbowuro, A. A., Mazraani, R., McCaughey, L. C., Huston, W. M., Gamble, A. B., & Tyndall, J. D. A. (2018). Stereochemical basis for the anti-chlamydial activity of the phosphonate protease inhibitor JO146. Tetrahedron, 74(12), 1184-1190. doi: 10.1016/j.tet.2017.10.031

Journal - Research Other

Agbowuro, A. A., Huston, W. M., Gamble, A. B., & Tyndall, J. D. A. (2018). Proteases and protease inhibitors in infectious diseases. Medicinal Research Reviews, 38(4), 1295-1331. doi: 10.1002/med.21475

Conference Contribution - Published proceedings: Abstract

Ruma, Y. N., Keniya, M. V., Sagatova, A. A., Tyndall, J., & Monk, B. (2018). Interactions between new azole drugs and their target enzyme. Proceedings of the New Zealand Microbiological Society (NZMS) New Zealand Society for Biochemistry and Molecular Biology (NZSBMB) Joint Annual Conference: Microbes & Molecules. (pp. 49). Retrieved from https://www.nzmsconference.org.nz

Keniya, M. V., Sagatova, A., Tyndall, J. D., & Monk, B. C. (2018). Co-expression of the cognate reductase for Candida albicans lanosterol 14α-demethylase enhances function in Saccharomyces cerevisiae. Proceedings of the 14th American Society for Microbiology Conference on Candida and Candidiasis. 52A. Retrieved from https://www.asm.org

Conference Contribution - Poster Presentation (not in published proceedings)

Agbowuro, A. A., Hwang, J., Peel, E., Mazraani, R., Springwald, A., Marsh, J. W., … Gamble, A. B., … Tyndall, J. D. A. (2018, August). Structure-activity relationships and binding optimization of Chlamydia HtrA inhibitors. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

Putha, L., Kok, L. K., Chen, K., Sagatova, A. A., Wilbanks, S. M., Gamble, A. B., Vernall, A. J., & Tyndall, J. D. (2018, August). New isothiocyanates: Covalent inhibitors of macrophage migration inhibitory factor. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

Ruma, Y., Keniya, M., Sagatova, A., Tyndall, J., & Monk, B. (2018, September). Interactions between new azole drugs and their target enzyme. Poster session presented at the Otago Spotlight Symposium on Infectious Disease, Wellington, New Zealand.

Conference Contribution - Verbal presentation and other Conference outputs

Lamichhane, R., de la Harpe, S., Harrop, T., Vernall, A., Tyndall, J., Dearden, P., Kirman, J., & Ussher, J. E. (2018, August). Differential regulation of MR1- and cytokine stimulated MAIT cells. Verbal presentation at the Queenstown Molecular Biology (QMB) and Australasian Society for Immunology New Zealand Branch (ASI-NZ) Joint Meeting, Queenstown, New Zealand.

2017

Journal - Research Article

Caramalho, R., Tyndall, J. D. A., Monk, B. C., Larentis, T., Lass-Flörl, C., & Lackner, M. (2017). Intrinsic short-tailed azole resistance in mucormycetes is due to an evolutionary conserved aminoacid substitution of the lanosterol 14α-demethylase. Scientific Reports, 7(1), 15898. doi: 10.1038/s41598-017-16123-9

Cooper, A., Singh, S., Hook, S., Tyndall, J. D. A., & Vernall, A. J. (2017). Chemical tools for studying lipid-binding class A G protein-coupled receptors. Pharmacological Reviews, 69(3), 316-353. doi: 10.1124/pr.116.013243

Matikonda, S. S., Fairhall, J. M., Tyndall, J. D. A., Hook, S., & Gamble, A. B. (2017). Stability, kinetic, and mechanistic investigation of 1,8-self-immolative cinnamyl ether spacers for controlled release of phenols and generation of resonance and inductively stabilized methides. Organic Letters, 19(3), 528-531. doi: 10.1021/acs.orglett.6b03695

Journal - Research Other

Marsh, J. W., Ong, V. A., Lott, W. B., Timms, P., Tyndall, J. D. A., & Huston, W. M. (2017). CtHtrA: The lynchpin of the chlamydial surface and a promising therapeutic target. Future Microbiology, 12(9), 817-829. doi: 10.2217/fmb-2017-0017

Conference Contribution - Published proceedings: Abstract

Agbowuro, A. A., Springwald, A., Hwang, J., Marsh, J. W., Mazraani, R., McCaugney, L. C., … Gamble, A. B., & Tyndall, J. D. A. (2017). Developing chlamydia-targeted protease inhibitors as a potential treatment for chlamydiosis. New Zealand Medical Journal, 130(1467), (pp. 105). Retrieved from http://www.nzma.org.nz/journal

Conference Contribution - Poster Presentation (not in published proceedings)

Cooper, A., Macdonald, C., Manning, J., Glass, M., Hook, S., Tyndall, J., & Vernall, A. (2017, September). Design, synthesis and pharmacological evaluation of fluorescent ligands as tools for studying cannabinoid type 2 receptor. Poster session presented at the 19th RSC/SCI Medicinal Chemistry Symposium, Cambridge, UK.

Lamichhane, R., de la Harpe, S., Harrop, T., Vernall, A., Tyndall, J., Dearden, P., Kirman, J., & Ussher, J. (2017, November). Differences in the effector function of MR1- and cytokine stimulated MAIT cells. Poster session presented at the 10th International CD1-MR1 Workshop, Napa, USA.

Conference Contribution - Verbal presentation and other Conference outputs

Ussher, J., Williams, T., Lamichhane, R., de la Harpe, S., Tyndall, J., & Vernall, A. (2017, November). Bacteria license antigen presenting cells for MR1-mediated MAIT cell activation. Verbal presentation at the 10th International CD1-MR1 Workshop, Napa, USA.

Monk, B. C., Tomasiak, T. M., Sagatova, A., Keniya, M. V., Wilson, R. K., Sabherwal, M., Tyndall, J. D. A., & Stroud, R. M. (2017, September). Structure-function analysis of the antifungal target sterol 14α-demethylase. Verbal presentation at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

2016

Journal - Research Article

Lawrence, A., Fraser, T., Gillett, A., Tyndall, J. D. A., Timms, P., Polkinghorne, A., & Huston, W. M. (2016). Chlamydia serine protease inhibitor, targeting HtrA, as a new treatment for Koala Chlamydia infection. Scientific Reports, 6, 31466 . doi: 10.1038/srep31466

Tyndall, J. D. A., Sabherwal, M., Sagatova, A. A., Keniya, M. V., Negroni, J., Wilson, R. K., Woods, M. A., … Monk, B. C. (2016). Structural and functional elucidation of yeast lanosterol 14α-demethylase in complex with agrochemical antifungals. PLoS ONE, 11(12), e0167485. doi: 10.1371/journal.pone.0167485

Sagatova, A. A., Keniya, M. V., Wilson, R. K., Sabherwal, M., Tyndall, J. D. A., & Monk, B. C. (2016). Triazole resistance mediated by mutations of a conserved active site tyrosine in fungal lanosterol 14α-demethylase. Scientific Reports, 6, 26213. doi: 10.1038/srep26213

Conference Contribution - Published proceedings: Abstract

Agbowuro, A. A., Springwald, A., Hwang, J., Marsh, J. W., Bogyo, M., Huston, W. M., Gamble, A. B., & Tyndall, J. D. A. (2016). Targeting a chlamydial proteolytic enzyme as a therapeutic approach to overcoming current treatment drawbacks. Proceedings of the Diagnostics, Drugs, Devices, Discovery (D4) Conference. Retrieved from http://www.otago.ac.nz/d4/index.html

Singh, S., Glenn, J. R., Hill, S. J., Tyndall, J. D. A., & Vernall, A. J. (2016). Illuminating the life of A₁ adenosine receptor. Proceedings of the Diagnostics, Drugs, Devices, Discovery (D4) Conference. Retrieved from http://www.otago.ac.nz/d4/index.html

Cooper, A. G., Macdonald, C., Glass, M., Hook, S., Tyndall, J. D. A., & Vernall, A. J. (2016). Development of tools for studying cannabinoid type 2 receptor: Design, synthesis and pharmacological evaluation of fluorescent ligands and intermediates. Proceedings of the Diagnostics, Drugs, Devices, Discovery (D4) Conference. Retrieved from http://www.otago.ac.nz/d4/index.html

Cooper, A. G., Macdonald, C., Glass, M., Hook, S., Tyndall, J. D. A., & Vernall, A. J. (2016). Development of fluorescent ligands as tools for studying cannabinoid type 2 receptor. Proceedings of the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists and the Molecular Pharmacology of G Protein-Coupled Receptors (ASCEPT-MPGPCR) Joint Scientific Meeting. 709. Retrieved from http://www.asceptasm.com/

Graham, D., Wilson, R., Keniya, M., Sagatova, A., Woods, M., Sabherwal, M., Tyndall, J., & Monk, B. (2016). The molecular basis of triazole inhibition of an antifungal target. Journal of Dental Research, 95(Spec Iss B), 1262. Retrieved from http://www.iadr.org/

Keniya, M. V., Wilson, R. K., Woods, M. A., Sabherwal, M., Sagatova, A. A., Tyndall, J. D. A., & Monk, B. C. (2016). Structure of the azole drug target from pathogenic fungi. Proceedings of the Sir John Walsh Research Institute Research Symposium. (pp. 13). Retrieved from http://www.otago.ac.nz/sjwri/news/otago621026

Sagatova, A., Wilson, R. K., Sabherwal, M., Keniya, M. V., Tyndall, J. D. A., & Monk, B. C. (2016). Investigating triazole mediated resistance in yeast. Proceedings of the Sir John Walsh Research Institute Research Symposium. (pp. 13). Retrieved from http://www.otago.ac.nz/sjwri/news/otago621026

Graham, D. O., Wilson, R. K., Keniya, M. V., Sagatova, A., Woods, M. A., Sabherwal, M., Tyndall, J. D. A., & Monk, B. C. (2016). The molecular basis of triazole inhibition of an antifungal target. Proceedings of the Sir John Walsh Research Institute Research Symposium. (pp. 12-13). Retrieved from http://www.otago.ac.nz/sjwri/news/otago621026

Conference Contribution - Poster Presentation (not in published proceedings)

Cooper, A. G., Macdonald, C., Glass, M., Hook, S., Tyndall, J. D. A., & Vernall, A. J. (2016, August-September). Development of fluorescent ligands as tools for studying cannabinoid type 2 receptor. Poster session presented at the European Federation for Medicinal Chemistry (EFMC) International Symposium on Medicinal Chemistry, Manchester, UK.

Singh, S., Tyndall, J. D. A., & Vernall, A. J. (2016, August-September). Development of selective fluorescent ligands for A₁ adenosine receptor as pharmacological tools. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Nelson, New Zealand.

Agbowuro, A. A., Sagatova, A. A., Wilbanks, S. M., Huston, W. M., Gamble, A. B., & Tyndall, J. D. A. (2016, August-September). Stereochemical basis of the anti-Chlamydial activity of JO146. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Nelson, New Zealand.

Conference Contribution - Verbal presentation and other Conference outputs

Tyndall, J. D. A., Agbowuro, A., Hwang, J., Springwald, A. H., Marsh, J., Gamble, A. B., & Huston, W. M. (2016, August-September). Targeting a multimeric protease for new Chlamydia therapeutics. Verbal presentation at the Queenstown Molecular Biology (QMB) Meetings, Nelson, New Zealand.

2015

Journal - Research Article

Kim, J. S., Brownjohn, P. W., Dyer, B. S., Beltramo, M., Walker, C. S., Hay, D. L., … Tyndall, J. D. A., & Anderson, G. M. (2015). Anxiogenic and stressor effects of the hypothalamic neuropeptide RFRP-3 are overcome by the NPFFR antagonist GJ14. Endocrinology, 156(11), 4152-4162. doi: 10.1210/en.2015-1532

Marsh, J. W., Wee, B. A., Tyndall, J. D. A., Lott, W. B., Bastidas, R. J., Caldwell, H. D., … Huston, W. M. (2015). A Chlamydia trachomatis strain with a chemically generated amino acid substitution (P370L) in the cthtrA gene shows reduced elementary body production. BMC Microbiology, 15, 194. doi: 10.1186/s12866-015-0533-2

Hellyer, S. D., Indurthi, D., Balle, T., Runder-Varga, V., Selwood, A. I., Tyndall, J. D. A., … Kerr, D. S. (2015). Pinnatoxins E, F and G target multiple nicotinic receptor subtypes. Journal of Neurochemistry, 135(3), 479-491. doi: 10.1111/jnc.13245

Sagatova, A. A., Keniya, M. V., Wilson, R. K., Monk, B. C., & Tyndall, J. D. A. (2015). Structural insights into binding of the antifungal drug fluconazole to Saccharomyces cerevisiae lanosterol 14α-demethylase. Antimicrobial Agents & Chemotherapy, 59(8), 4982-4989. doi: 10.1128/aac.00925-15

Spencer, E. S., Dale, E. J., Gommans, A. L., Rutledge, M. T., Vo, C. T., Nakatani, Y., Gamble, A. B., Smith, R. A. J., Wilbanks, S. M., Hampton, M. B., & Tyndall, J. D. A. (2015). Multiple binding modes of isothiocyanates that inhibit macrophage migration inhibitory factor. European Journal of Medicinal Chemistry, 93, 501-510. doi: 10.1016/j.ejmech.2015.02.012

Conference Contribution - Published proceedings: Abstract

Singh, S., Tyndall, J. D. A., & Vernall, A. (2015). Development of selective fluorescent ligands for A1AR as pharmacological tools. Proceedings of the Diagnostic Drug Device Discovery (D4) Conference. Retrieved from https://www.regonline.com.au/builder/site/Default.aspx?EventID=1758070

Cooper, A., Hook, S., Tyndall, J. D. A., & Vernall, A. (2015). Development of fluorescent ligands as tools for studying the cannabinoid type 2 receptor. Proceedings of the Diagnostic Drug Device Discovery (D4) Conference. Retrieved from https://www.regonline.com.au/builder/site/Default.aspx?EventID=1758070

Spencer, E., Dickerhof, N., Tyndall, J., Bernhagen, J., Kettle, A., & Hampton, M. (2015). Assessing inhibition of macrophage migration inhibitory factor by isothiocyanates. Free Radical Biology & Medicine, 86(Suppl. 1), (pp. S42-S43). doi: 10.1016/j.freeradbiomed.2015.07.145

Conference Contribution - Verbal presentation and other Conference outputs

Tyndall, J. D. A., Sagatova, A., Keniya, M. V., Sabherwal, M., Wilson, R., Negroni, J., … Monk, B. C. (2015, August-September). Structural studies of the membrane protein CYP51 reveals resistance mechanism against short-chain azole antifungals. Verbal presentation at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

2014

Journal - Research Article

Dickerhof, N., Magon, N. J., Tyndall, J. D. A., Kettle, A. J., & Hampton, M. B. (2014). Potent inhibition of macrophage migration inhibitory factor (MIF) by myeloperoxidase-dependant oxidation of epicatechins. Biochemical Journal, 462(2), 303-314. doi: 10.1042/BJ20140612

Monk, B. C., Tomasiak, T. M., Keniya, M. V., Huschmann, F. U., Tyndall, J. D. A., O'Connell, III, J. D., Cannon, R. D., … Stroud, R. M. (2014). Architecture of a single membrane spanning cytochrome P450 suggests constraints that orient the catalytic domain relative to a bilayer. PNAS, 111(10), 3865-3870. doi: 10.1073/pnas.1324245111

Conference Contribution - Published proceedings: Abstract

Sagatova, A., Keniya, M., Huschmann, F., Wilbanks, S., Cannon, R., Tyndall, J., & Monk, B. (2014). Triazole drug target structures in a resistant yeast strain. New Zealand Medical Journal, 127(1404). Retrieved from http://www.nzma.org.nz/journal

Tyndall, J. D. A., Spencer, E. S., Dale, E. J., Gommans, A. L., Rutledge, M. T., Vo, C. T., Nakatani, Y., Gamble, A. B., Smith, R. A. J., Wilbanks, S. M., & Hampton, M. B. (2014). Multiple binding modes of isothiocyanate inhibitors of macrophage migration inhibitory factor define structure activity relationships. Proceedings of the CRYSTAL29: 29th Biennial Conference of the Society of Crystallographers in Australia and New Zealand (SCANZ). (pp. 88). Retrieved from http://www.crystal29.com/

Tyndall, J. D. A., Sagatova, A., Tomasiak, T. M., Keniya, M. V., Huschmann, F. U., O'Connell, III, J. D., … Cannon, R. D., … Monk, B. C. (2014). Structures of full-length bitopic membrane protein CYP51 from Saccharomyces cerevisiae provide insight into substrate and drug binding and mutations affecting antifungal susceptibility. Proceedings of the CRYSTAL29: 29th Biennial Conference of the Society of Crystallographers in Australia and New Zealand (SCANZ). (pp. 50). Retrieved from http://www.crystal29.com/

Conference Contribution - Poster Presentation (not in published proceedings)

Kim, J. S., Brownjohn, P. W., Dyer, B. S., Compton, B. J., Beltramo, M., Painter, G. F., Tyndall, J. D., & Anderson, G. M. (2014, August). In vitro and in vivo analyses of novel neuropeptide FF receptor antagonists. Poster session presented at the International Congress of Neuroendocrinology (ICN), Sydney, Australia.

Kim, J. S., Brownjohn, P. W., Dyer, B. S., Compton, B. J., Painter, G. F., Tyndall, J. D., & Anderson, G. M. (2014, August). Neuropeptide FF receptors as therapeutic targets. Poster session presented at the Medical Sciences Congress (MedSci), Queenstown, New Zealand.

Sagatova, A., Keniya, M. V., Huschmann, F. U., Wilbanks, S. M., Cannon, R. D., Tyndall, J. D. A., & Monk, B. C. (2014, May). Egr11p structure in triazole resistant and susceptible strains of yeast. Poster session presented at the International Association for Dental Research (IADR) New Zealand Section Student Poster Competition, Dunedin, New Zealand.

Tyndall, J. D. A., Spencer, E. S., Dale, E. J., Gommans, A. L., Rutledge, M. T., Vo, C. T., Nakatani, Y., Gamble, A. B., Smith, R. A. J., Wilbanks, S. M., & Hampton, M. B. (2014, August). Multiple binding modes of isothiocyanate inhibitors of macrophage migration inhibitory factor define design strategies. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

Sagatova, A., Keniya, M., Huschmann, F., Wilbanks, S., Cannon, R., Tyndall, J., & Monk, B. (2014, September). Erg11p structure in a triazole resistant yeast strain. Poster session presented at the Division of Health Sciences Research Forum: Learning Different Research Languages, Dunedin, New Zealand.

Conference Contribution - Verbal presentation and other Conference outputs

Monk, B. C., Tomasiak, T. M., Cannon, R. D., Sagatova, A., Keniya, M. V., Huschmann, F. U., Tyndall, J. D. A., … Stroud, R. M. (2014, November). A target structure to invigorate antifungal discovery. Verbal presentation at the Frontiers of Biology Satellite Meeting: From Protein Structure and Function to Drugs, Wellington, New Zealand.

Tyndall, J. D. A., Sagatova, A., Tomasiak, T. M., Keniya, M. V., Huschmann, F. U., O'Connell, III, J. D., … Cannon, R. D., … Monk, B. C. (2014, April). Structures of full-length bitopic membrane protein CYP51 from Saccharomyces cerevisiae provide insight into substrate and drug binding and mutations affecting antifungal susceptibility. Verbal presentation at the 29th Biennial Conference of the Society of Crystallographers in Australia and New Zealand (SCANZ), O'Reilly's Rainforest Retreat, Australia.

Tyndall, J. (2014, July). Structural resolution of the full-length bitopic membrane protein CYPS1 mono-oxygenase from Saccharomyces cerevisiae: Substrate, drug binding and mutations affecting antifungal susceptibility. Verbal presentation at the Oxygen Theme Meeting, Christchurch, New Zealand.

Tyndall, J. (2014, June-July). Multiple binding modes of isothiocyanate inhibitors of macrophage migration inhibitory factor define structure activity relationships. Verbal presentation at the New Zealand Structural Biology Meeting, Hanmer Springs, New Zealand.

2013

Journal - Research Article

Marsh, J. W., Lott, W. B., Tyndall, J. D. A., & Huston, W. M. (2013). Proteolytic activation of Chlamydia trachomatis HTRA is mediated by PDZ1 domain interactions with protease domain loops L3 and LC and beta strand β5. Cellular & Molecular Biology Letters, 18(4), 522-537. doi: 10.2478/s11658-013-0103-2

Rawal, M. K., Khan, M. F., Kapoor, K., Goyal, N., Sen, S., Saxena, A. K., … Tyndall, J. D. A., Monk, B. C., Cannon, R. D., … Prasad, R. (2013). Insight into pleiotropic drug resistance ATP-binding cassette pump drug transport through mutagenesis of Cdr1p transmembrane domains. Journal of Biological Chemistry, 288(34), 24480-24493. doi: 10.1074/jbc.M113.488353

Awasthi, A., Woolley, A. G., Lecomte, F. J., Hung, N., Baguley, B. C., Wilbanks, S. M., Jeffs, A. R., & Tyndall, J. D. A. (2013). Variable expression of GLIPR1 correlates with invasive potential in melanoma cells. Frontiers in Oncology, 3, 225. doi: 10.3389/fonc.2013.00225

Shankar, M., Wilbanks, S. M., Nakatani, Y., Monk, B. C., & Tyndall, J. D. A. (2013). Catalysis product captured in lumazine synthase from the fungal pathogen Candida glabrata. Acta Crystallographica Section D, 69(8), 1580-1586. doi: 10.1107/S0907444913010949

Gloeckl, S., Ong, V. A., Patel, P., Tyndall, J. D. A., Timms, P., Beagley, K. W., … Huston, W. M. (2013). Identification of a serine protease inhibitor which causes inclusion vacuole reduction and is lethal to Chlamydia trachomatis. Molecular Microbiology, 89(4), 676-689. doi: 10.1111/mmi.12306

Vellas, S. K., Lewis, J. E. M., Shankar, M., Sagatova, A., Tyndall, J. D. A., Monk, B. C., Fitchett, C. M., Hanton, L. R., & Crowley, J. D. (2013). [Fe₂L₃]⁴⁺ cylinders derived from bis(bidentate) 2-pyridyl-1,2,3-triazole "click" ligands: Synthesis, structures and exploration of biological activity. Molecules, 18(6), 6383-6407. doi: 10.3390/molecules18066383

Keniya, M. V., Cannon, R. D., Nguyễn, Ấ., Tyndall, J. D. A., & Monk, B. C. (2013). Heterologous expression of Candida albicans Pma1p in Saccharomyces cerevisiae. FEMS Yeast Research, 13(3), 302-311. doi: 10.1111/1567-1364.12035

Conference Contribution - Published proceedings: Abstract

Huschmann, F. U., Tomasiak, T. M., Keniya, M. V., O'Connell, III, J. D., Luckner, S. R., Krause, K., Cannon, R. D., … Tyndall, J. D. A., & Monk, B. C. (2013). Antifungal drug discovery: Crystallization of the cytochrome P450 triazole target. Proceedings of the Australasian Pharmaceutical Science Association (APSA) Conference. Retrieved from http://apsa-online.org/home.html

Huschmann, F. U., Tomasiak, T. M., Keniya, M. V., O'Connell, III, J. D., Luckner, S. R., Krause, K., Cannon, R. D., … Tyndall, J. D. A., & Monk, B. C. (2013). Crystallization of Erg11p: The cytochrome P450 target of triazole antifungals. Acta Crystallographica Section A, A69, (pp. s64). [Abstract]

Cannon, R., Niimi, K., Lamping, E., Huschmann, F. U., Niimi, M., Keniya, M. V., Tyndall, J. D. A., Holmes, A. R., & Monk, B. C. (2013). Overcoming antifungal drug resistance. Proceedings of the Sir John Walsh Research Institute Research Day. (pp. 6). Retrieved from http://sjwri.otago.ac.nz/research/sjwri/

Conference Contribution - Poster Presentation (not in published proceedings)

Spencer, E. S., Dale, E., Smith, R. A. J., Gamble, A. B., Tyndall, J. D. A., Rutledge, M. T., Wilbanks, S. M., Dickerhof, N., Kettle, A. J., & Hampton, M. B. (2013, August). Assessing inhibition of macrophage migration inhibitory factor by novel isothiocyanates. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

Monk, B. C., Tomasiak, T. M., Keniya, M. V., Cannon, R. D., Huschmann, F. U., Tyndall, J. D. A., … Stroud, R. M. (2013, August). Crystal structures of full-length Saccharomyces cerevisiae Erg11p give insight into triazole and substrate binding. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

Gommans, A., Hampton, M. B., Tyndall, J. D. A., & Wilbanks, S. M. (2013, August). Improved-resolution structure of macrophage migration inhibitory factor complexed with phenethyl isothiocyanate. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

Conference Contribution - Verbal presentation and other Conference outputs

Mansfield, R. E., Lo, A. T. Y., Li, N., Tyndall, J. D. A., & Dixon, N. E. (2013, February). Targeting a bacterial protein interaction 'hub' in the search for a new class of antibiotics. Verbal presentation at the 38th Lorne Conference on Protein Structure and Function, Lorne, Australia.

Gommans, A. L., Tyndall, J. D. A., Hampton, M. B., & Wilbanks, S. M. (2013, February). Improved resolution of macrophage migration inhibitory factor complexed with phenethyl isothiocyanate. Verbal presentation at the 38th Lorne Conference on Protein Structure and Function, Lorne, Australia.

2012

Journal - Research Article

Tyndall, J. D. A., Lue, H., Rutledge, M. T., Bernhagen, J., Hampton, M. B., & Wilbanks, S. M. (2012). Macrophage migration inhibitory factor covalently complexed with phenethyl isothiocyanate. Acta Crystallographica Section F, 68(9), 999-1002. doi: 10.1107/s1744309112030552

Niimi, K., Harding, D. R. K., Holmes, A. R., Lamping, E., Niimi, M., Tyndall, J. D. A., Cannon, R. D., & Monk, B. C. (2012). Specific interactions between the Candida albicans ABC transporter Cdr1p ectodomain and a D-octapeptide derivative inhibitor. Molecular Microbiology, 85(4), 747-767. doi: 10.1111/j.1365-2958.2012.08140.x

Conference Contribution - Published proceedings: Abstract

Spencer, E., Tyndall, J., Smith, R. A. J., & Hampton, M. (2012). Biological properties of isothiocyanates. Proceedings of the Oxygen Theme Meeting. (pp. 21). Dunedin, New Zealand: University of Otago. Retrieved from https://www.otago.ac.nz/research/otago051864.pdf

Conference Contribution - Poster Presentation (not in published proceedings)

Tomasiak, T. M., Monk, B. C., Keniya, M. V., Huschmann, F. U., Tyndall, J. D. A., O'Connell, III, J. D., Cannon, R. D., … Stroud, R. M. (2012, November). Structure of a full-length bitopic single membrane spanning cytochrome p450: The antifungal target lanosterol 14-alpha demethylase. Poster session presented at the 4th Membrane Protein Technologies Meeting: NIH Roadmap to Membrane Protein Structures and Complexes, San Francisco, CA.

Huschmann, F., Monk, B. C., Cannon, R. D., & Tyndall, J. D. A. (2012, August). Overcoming resistance in fungal pathogens: Towards crystallization of the azole target from Candida albicans. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

Conference Contribution - Verbal presentation and other Conference outputs

Monk, B. C., Tomasiak, T. M., Keniya, M. V., Huschmann, F. U., Tyndall, J. D. A., O'Connell, III, J. D., Cannon, R. D., … Stroud, R. M. (2012, November). A cytochrome P450 monospanner in the works: Structure of full-length yeast lanosterol 14α-demethylase. Verbal presentation at the 4th Membrane Protein Technologies Meeting: NIH Roadmap to Membrane Protein Structures and Complexes, San Francisco, CA.

2011

Chapter in Book - Research

Marsh, J., Gloeckl, S., Tyndall, J., & Huston, W. M. (2011). The role of HtrA as a chaperone and protease in bacterial pathogenesis. In L. V. Berhardt (Ed.), Advances in Medicine and Biology (Vol. 27). (pp. 87-121). New York: Nova Science.

Journal - Research Article

Beggs, K. T., Tyndall, J. D. A., & Mercer, A. R. (2011). Honey bee dopamine and octopamine receptors linked to intracellular calcium signaling have a close phylogenetic and pharmacological relationship. PLoS ONE, 6(11), e26809. doi: 10.1371/journal.pone.0026809

Huston, W. M., Tyndall, J. D. A., Lott, W. B., Stansfield, S. H., & Timms, P. (2011). Unique residues involved in activation of the multitasking protease/chaperone HtrA from Chlamydia trachomatis. PLoS ONE, 6(9), e24547. doi: 10.1371/journal.pone.0024547

Matthews, H., Ranson, M., Tyndall, J. D. A., & Kelso, M. J. (2011). Synthesis and preliminary evaluation of amiloride analogs as inhibitors of the urokinase-type plasminogen activator (uPA). Bioorganic & Medicinal Chemistry Letters, 21(22), 6760-6766. doi: 10.1016/j.bmcl.2011.09.044

Suetani, R. J., Sorrenson, B., Tyndall, J. D. A., Williams, M. J. A., & McCormick, S. P. A. (2011). Homology modeling and functional testing of an ABCA1 mutation causing Tangier disease. Atherosclerosis, 218(2), 404-410. doi: 10.1016/j.atherosclerosis.2011.06.019

Conference Contribution - Poster Presentation (not in published proceedings)

Suetani, R., Sorrenson, B., Tyndall, J., Williams, M., & McCormick, S. (2011, September). Homology modelling and functional testing of ABCA1 mutations. Poster session presented at the Queenstown Molecular Biology (QMB) Meetings, Queenstown, New Zealand.

Conference Contribution - Verbal presentation and other Conference outputs

Tyndall, J. (2011, March). Differential expression of GLIPR1 correlates with invasive potential in melanoma cells. Verbal presentation at the New Zealand/Singapore Cancer Symposium, Dunedin, New Zealand.

Huston, W. M., Tyndall, J. D. A., Lott, W. B., Stansfield, S., & Timms, P. (2011, October). A novel activation mechanism for the multitasking protease/chaperone HTRA from chlamydia trachomatis. Verbal presentation at the Seventh International Proteolysis Society General Meeting, San Diego, CA.

Tyndall, J. (2011, December). Drug leads, drug targets and drug design. Verbal presentation at the Maurice Wilkins Centre for Molecular Biodiscovery Workshop: Celebrating Collaboration in Biomedical Research, Dunedin, New Zealand.

Tyndall, J. D. A., Dale, E. J., Spencer, E. S., Falvey, J. D., Smith, R. A. J., & Hampton, M. B. (2011, November-December). Isothiocyanate inhibitors of the proinflammatory cytokine macrophage migration inhibitory factor. Verbal presentation at the New Zealand Institute of Chemistry (NZIC) Conference, Hamilton, New Zealand.

2010

Chapter in Book - Research

Tyndall, J. D. A., Kelso, M. J., & Ranson, M. (2010). Inhibitors of the plasminogen activation system: Promising new agents for suppressing breast cancer metastasis. In Atta-ur-Rahman & M. I. Choudhary (Eds.), Frontiers in anti-cancer drug discovery (Vol. 1). (pp. 55-78). Bentham Science.

Journal - Research Article

Loughlin, W. A., Tyndall, J. D. A., Glenn, M. P., Hill, T. A., & Fairlie, D. P. (2010). Update 1 of: Beta-strand mimetics. Chemical Reviews, 110(6), PR32-PR69. doi: 10.1021/cr900395y

Madala, P. K., Tyndall, J. D. A., Nall, T., & Fairlie, D. P. (2010). Update 1 of: Proteases universally recognize beta strands in their active sites. Chemical Reviews, 110(6), PR1-PR31. doi: 10.1021/cr900368a

Nisa, S., Blokpoel, M. C. J., Robertson, B. D., Tyndall, J. D. A., Lun, S., Bishai, W. R., & O'Toole, R. (2010). Targeting the chromosome partitioning protein ParA in tuberculosis drug discovery. Journal of Antimicrobial Chemotherapy, 65(11), 2347-2358. doi: 10.1093/jac/dkq311

Ruiz-Gómez, G., Tyndall, J. D. A., Pfeiffer, B., Abbenante, G., & Fairlie, D. P. (2010). Update 1 of: Over one hundred peptide-activated G protein-coupled receptors recognize ligands with turn structure. Chemical Reviews, 110, PR1-PR41. doi: 10.1021/cr900344w

Sawant, P. M., Tyndall, J. D. A., Holland, P. T., Peake, B. M., Mountfort, D. O., & Kerr, D. S. (2010). In vivo seizure induction and affinity studies of domoic acid and isodomoic acids-D, -E and -F. Neuropharmacology, 59, 129-138. doi: 10.1016/j.neuropharm.2010.03.019

Conference Contribution - Published proceedings: Abstract

Nguyen, A., Milne, T., Monk, B., & Tyndall, J. (2010). A model system for heterologous expression of cysteine-rich secretory proteins, antigen 5 and pathogenesis-related group 1 proteins in E. coli. New Zealand Medical Journal, 123(1321). Retrieved from http://journal.nzma.org.nz/journal/123-1321/4329/content.pdf

Conference Contribution - Verbal presentation and other Conference outputs

Brown, K. K., Blaikie, F. H., Smith, R. A. J., Tyndall, J. D. A., Lue, H., Bernhagen, J., Winterbourn, C. C., & Hampton, M. B. (2010, November-December). N-terminal proline of macrophage migration inhibitory factor as a biological target of isothiocyanates. Verbal presentation at the Society for Free Radical Research (SFRR) Australasia 19th Annual Conference, Akaroa, New Zealand.

Other Research Output

Tyndall, J. (2010, February). HtrA: A new potential drug target in Chlamydia trachomatis. University of Otago School of Pharmacy Seminar. Dunedin, New Zealand. [Department Seminar].

2009

Journal - Research Article

Brown, K. K., Blaikie, F. H., Smith, R. A. J., Tyndall, J. D. A., Lue, H., Bernhagen, J., Winterbourn, C. C., & Hampton, M. B. (2009). Direct modification of the proinflammatory cytokine macrophage migration inhibitory factor by dietary isothiocyanates. Journal of Biological Chemistry, 284(47), 32425-32433. doi: 10.1074/jbc.M109.047092

Westphal, D., Ledgerwood, E. C., Tyndall, J. D. A., Hibma, M. H., Ueda, N., Fleming, S. B., & Mercer, A. A. (2009). The orf virus inhibitor of apoptosis functions in a Bcl-2-like manner, binding and neutralizing a set of BH3-only proteins and active Bax. Apoptosis, 14(11), 1317-1330. doi: 10.1007/s10495-009-0403-1

Fry, B. G., Roelants, K., Champagne, D. E., Scheib, H., Tyndall, J. D. A., …, & Rodríguez de la Vega, R. C. (2009). The toxicogenomic multiverse: Convergent recruitment of proteins into animal venoms. Annual Review of Genomics & Human Genetics, 10, 483-511. doi: 10.1146/annurev.genom.9.081307.164356

Lamping, E., Ranchod, A., Nakamura, K., Tyndall, J. D. A., Niimi, K., Holmes, A. R., Niimi, M., & Cannon, R. D. (2009). Abc1p is a multidrug efflux transporter that tips the balance in favor of innate azole resistance in Candida krusei. Antimicrobial Agents & Chemotherapy, 53(2), 354-369. doi: 10.1128/AAC.01095-08

Conference Contribution - Published proceedings: Abstract

Brace, R. J., Williams, M. J., Tyndall, J. D. A., Sviridov, D., Mukhamedova, N., Albrecht, C., & McCormick, S. P. A. (2009). Characterisation of a novel Tangier disease ABCA1 protein. Proceedings of the ComBio2009 Conference. [CD-ROM] [Abstract]

Nguyen, A. B., Milne, T. J., Monk, B. C., & Tyndall, J. D. A. (2009). Re-engineering Tex31 for expression and purification. Proceedings of the ComBio2009 Conference. [CD-ROM] [Abstract]

Tyndall, J. D. A., Awasthi, A., Jeffs, A., & Wilbanks, S. M. (2009). GLIPR1 is differentially expressed in melanoma cells and correlates with invasive potential. Proceedings of the ComBio2009 Conference. [CD-ROM] [Abstract]

Kerr, D., Sawant, P. M., Tyndall, J., Mountfort, D. O., & Holland, P. (2009). Quantitative structure-activity relationships for domoic acid and its isomers. Proceedings of the Society for Neuroscience 39th Annual Meeting. SfN. Retrieved from http://www.abstractsonline.com/plan/AdvancedSearch.aspx

Lees, G., Dixon, C., & Tyndall, J. (2009). Exploring the mechanisms for the neurotoxicity of Efavirenz (EFV). Proceedings of the Webster Centre for Infectious Diseases Symposium. WCID. Retrieved from http://www.webstercentre.otago.ac.nz/WCIDSymposiumProgramme.pdf

Conference Contribution - Verbal presentation and other Conference outputs

Gloeckl, S., Tyndall, J. D. A., Timms, P., & Huston, W. M. (2009, September). Characterisation of the role of the chlamydial serine protease, HtrA, in growth and virulence by identifying and examining its native substrates. Verbal presentation at the Australian Society for Microbiology Conference: The Molecular Biology of Bacterial Pathogens (BacPath 10), Barossa Valley, Australia.

Tyndall, J. D. A., Timms, P., & Huston, W. M. (2009, October). Development of an assay for testing substrate specificity determinants for Chlamydia trachomatis heat activated serine protease HtrA. Verbal presentation at the Sixth General Meeting of the International Proteolysis Society, Surfers Paradise, Australia.

Sawant, P. M., Tyndall, J., Mountfort, D. O., Holland, P. T., & Kerr, D. S. (2009, September). In vivo potency, receptor binding and molecular modeling identify structure-activity relationships for domoic acid and its isomers. Verbal presentation at the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists New Zealand Annual Scientific Meeting, Dunedin, New Zealand.

Lees, G., Dixon, C., Maggo, S., Clark, D., Tyndall, J., & Strandell, J. (2009, September). Modulation of ion channels by the antiviral drug efavirenz. Verbal presentation at the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists New Zealand Annual Scientific Meeting, Dunedin, New Zealand.

Awasthi, A., Tyndall, J. D. A., Jeffs, A., & Wilbanks, S. M. (2009, February). Glioma pathogenesis related protein: A survival factor for gliomas and melanomas. Verbal presentation at the New Zealand Chapter of the Controlled Release Society 11th Conference on Formulation and Delivery of Bioactives, Dunedin, New Zealand.

2008

Journal - Research Article

Tyndall, J. D. A., Kelso, M. J., Clingan, P., & Ranson, M. (2008). Peptides and small molecules targeting the plasminogen activation system: Towards prophylactic anti-metastasis drugs for breast cancer. Recent Patents on Anti-Cancer Drug Discovery, 3(1), 1-13.

Ashton, J. C., Wright, J. L., McPartland, J. M., & Tyndall, J. D. A. (2008). Cannabinoid CB1 and CB2 receptor ligand specificity and the development of CB2-selective agonists. Current Medicinal Chemistry, 15, 1428-1443.

Tyndall, J. D. A., Pattenden, L. K., Reid, R. C., Hu, S.-H., Alewood, D., Alewood, P. F., … Martin, J. L. (2008). Crystal structures of highly constrained substrate and hydrolysis products bound to HIV-1 protease: Implications for the catalytic mechanism. Biochemistry, 47, 3736-3744.

Conference Contribution - Published proceedings: Abstract

Ashton, J. C., Wright, J. L., McPartland, J. M., Gertsch, J., & Tyndall, J. D. A. (2008). Development of drugs targeting the cannabinoid CB2 receptor for therapeutic use. Proceedings of the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists New Zealand Annual Scientific Meeting. ASCEPT. Retrieved from http://phal.otago.ac.nz/ascept_docos/programme%202008.pdf

Tyndall, J. D. A., Reid, R. C., Monk, P. N., & Fairlie, D. P. (2008). Targeting inflammation via the complement system: Designing antagonists against C5A. Proceedings of the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists New Zealand Annual Scientific Meeting. ASCEPT. Retrieved from http://phal.otago.ac.nz/ascept_docos/programme%202008.pdf

Conference Contribution - Poster Presentation (not in published proceedings)

Nguyen, A. B., Milne, T. J., Tyndall, J. D. A., & Monk, B. C. (2008, November-December). Expression of recombinant Tex31. Poster session presented at the New Zealand Institute of Chemistry, New Zealand Society for Biochemistry and Molecular Biology and the New Zealand Society of Plant Biologists Combined Conference, Dunedin, New Zealand.

Conference Contribution - Verbal presentation and other Conference outputs

Awasthi, A., Wilbanks, S. M., Jeffs, A., & Tyndall, J. D. A. (2008, November-December). Is glioma pathogenesis related protein a survival factor for gliomas? Verbal presentation at the New Zealand Institute of Chemistry, New Zealand Society for Biochemistry and Molecular Biology and the New Zealand Society of Plant Biologists Combined Conference, Dunedin, New Zealand.

2007

Journal - Research Article

Pearl, E. J., Tyndall, J. D. A., Poulter, R. T. M., & Wilbanks, S. M. (2007). Sequence requirements for splicing by the Cne PRP8 intein. FEBS Letters, 581, 3000-3004.

Gee, C. L., Drinkwater, N., Tyndall, J. D. A., Grunewald, G. L., Wu, Q., McLeish, M. J., & Martin, J. L. (2007). Enzyme adaptation to inhibitor binding: A cryptic binding site in phenylethanolamine N-methyltransferase. Journal of Medicinal Chemistry, 50(20), 4845-4853.

Journal - Professional & Other Non-Research Articles

Tyndall, J. D. A., & Duffull, S. B. (2007). New drugs targeting GPCRs: Recent agonists and antagonists in the clinic. Screening, 1, 22-25.

Conference Contribution - Published proceedings: Abstract

Clarkson, A. N., Koishi, K., Tyndall, J. D. A., & McLennan, I. S. (2007). The MIS type-II receptor, MISRII, has splice variants in the CNS. In J. G. Anson (Ed.), Proceedings of the 25th International Australasian Winter Conference on Brain Research. 25, (pp. 62). AWCBR. Retrieved from http://psy.otago.ac.nz/awcbr/Abstracts/2007Abstracts.pdf

Conference Contribution - Poster Presentation (not in published proceedings)

Awasthi, A., Slobbe, L., Tyndall, J. D. A., & Wilbanks, S. M. (2007, August). Modelling and expression of Glioma pathogenesis related protein: A potential drug target for Gliomas. Poster session presented at the 17th Queenstown Molecular Biology Meeting, Queenstown, New Zealand.

Wilbanks, S. M., Pearl, E., Tyndall, J. D. A., & Poulter, R. T. M. (2007, August). Conformational shifts contribute to protein splicing by Cne PRP8, an intein of the human pathogen Cryptococcus neoformans. Poster session presented at the 17th Queenstown Molecular Biology Meeting, Queenstown, New Zealand.

Tyndall, J. D. A., McCormick, S., & Monk, B. C. (2007, February). The ABC of mapping sequence to structure via homology modelling: A tale of two transporters. Poster session presented at the Proteins: Structure, Function and Assembly in Health and Disease, Rotorua, New Zealand.

Conference Contribution - Verbal presentation and other Conference outputs

Tyndall, J. (2007, December). Crystal structures of highly constrained substrate and hydrolysis products bound to HIV-1 protease: Implications for catalytic mechanism and drug design. Verbal presentation at the Webster Centre for Molecular Research in Infectious Diseases Mini-Symposium, Dunedin, New Zealand.

2006

Journal - Research Article

Sobhani, A. M., Amini, S. R., Tyndall, J. D. A., Azizi, E., Daneshtalab, M., & Khalaj, A. (2006). A theory of mode of action of azolylalkylquinolines as DNA binding agents using automated flexible ligand docking. Journal of Molecular Graphics & Modelling, 25, 459-469.

Kahnberg, P., Lucke, A. J., Glenn, M. P., Boyle, G. M., Tyndall, J. D. A., Parsons, P. G., & Fairlie, D. P. (2006). Design, synthesis, potency, and cytoselectivity of anticancer agents derived by parallel synthesis from α-aminosuberic acid. Journal of Medicinal Chemistry, 49, 7611-7622.

Conference Contribution - Published proceedings: Abstract

Monk, P. N., Higginbottom, A., Madala, P. K., Tyndall, J. D. A., Stoermer, M., & Fairlie, D. P. (2006). Defining the ligand binding site on the human C5a receptor. Proceedings of the American Chemical Society Meeting. 231, (pp. U408). Washington, DC: ACS. [Abstract]

Drinkwater, N., Gee, C. L., Tyndall, J. D., Grunewald, G. L., Wu, Q., McLeish, M. J., & Martin, J. L. (2006). Encountering conformational changes in structure-based inhibitor design. Proceedings of the Australian Society for Biochemistry and Molecular Biology (ComBio). 38. Retrieved from http://www.asbmb.org.au/cgi-bin/combio/combio2006-abstract-search.cgi

Conference Contribution - Poster Presentation (not in published proceedings)

Drinkwater, N., Gee, C. L., Tyndall, J. D., Grunewald, G. L., Qian, W., McLeish, M. J., & Martin, J. L. (2006, November). Coupling crystallography with kinetic studies leads to identification of a previously unknown binding pocket. Poster session presented at the Joint Conference of the Asian Crystallographic Association and the Crystallographic Society of Japan, Epochal Tsukuba, Japan.

Conference Contribution - Verbal presentation and other Conference outputs

Tyndall, J. (2006, October). Investigating CAP proteins. Verbal presentation at the Pharmacy School Seminar Series, Dunedin, New Zealand.

2005

Journal - Research Article

Wu, Q., Gee, C. L., Lin, F., Tyndall, J. D., Martin, J. L., Grunewald, G. L., & McLeish, M. J. (2005). Structural, mutagenic, and kinetic analysis of the binding of substrates and inhibitors of human phenylethanolamine N-methyltransferase. Journal of Medicinal Chemistry, 48(23), 7243-7252.

Gee, C. L., Tyndall, J. D. A., Grunewald, G. L., Wu, Q., McLeish, M. J., & Martin, J. L. (2005). Mode of binding of methyl acceptor substrates to the adrenaline-synthesizing enzyme phenylethanolamine N-methyltransferase: Implications for catalysis. Biochemistry, 44, 16875-16885.

Gee, C. L., Nourse, A., Hsin, A.-Y., Wu, Q., Tyndall, J. D., Grunewald, G. L., … Martin, J. L. (2005). Disulfide-linked dimers of human adrenaline synthesizing enzyme PNMT are catalytically active. Biochimica et Biophysica Acta: Proteins & Proteomics, 1750, 82-92.

Tyndall, J. D. A., & Sandilya, R. (2005). GPCR agonists and antagonists in the clinic. Medicinal Chemistry, 1, 405-421.

Chappell, K. J., Nall, T. A., Stoermer, M. J., Fang, N.-X., Tyndall, J. D. A., Fairlie, D. P., & Young, P. R. (2005). Site-directed mutagenesis and kinetic studies of the West Nile virus NS3 protease identify key enzyme-substrate interactions. Journal of Biological Chemistry, 280(4), 2896-2903.

Higginbottom, A., Cain, S. A., Woodruff, T. M., Proctor, L. M., Madala, P. K., Tyndall, J. D. A., … Monk, P. N. (2005). Comparative agonist/antagonist responses in mutant human C5a receptors define the ligand binding site. Journal of Biological Chemistry, 280(18), 17831-17840.

Tyndall, J. D. A., Pfeiffer, B., Abbenante, G., & Fairlie, D. P. (2005). Over one hundred peptide-activated G protein-coupled receptors recognize ligands with turn structure. Chemistry Review, 105, 793-826.

Tyndall, J. D. A., Nall, T., & Fairlie, D. P. (2005). Proteases universally recognize beta strands in their active sites. Chemistry Review, 105, 973-999.

Conference Contribution - Published proceedings: Abstract

Tyndall, J., Malack, S., Holland, P., Mountfort, D., & Kerr, S. (2005). 3D-QSAR of AMPA and kainate ionotropic glutamate receptor agonists. Proceedings of the International Chemical Congress of Pacific Basin Societies. (pp. 104). [Abstract]

Fairlie, D. P., Tyndall, J., Abbenante, G., & Pfeiffer, B. (2005). Over 100 peptide-activated GPCRS recognize turn motifs in ligands. Proceedings of the 229th American Chemical Society Division of Medicinal Chemistry National Meeting. [Abstract]

Conference Contribution - Poster Presentation (not in published proceedings)

Gee, C. L., Tyndall, J., Grunewald, G. L., McLeish, M. J., & Martin, J. L. (2005, August). A dramatic side chain movement in adrenaline-synthesising PNMT: Implications for drug design. Poster session presented at the XX Congress of the International Union of Crystallography: Congress and General Assembly, Florence.

Amini, S. R., Tyndall, J., & Daneshtalab, M. (2005, May). Primary DNA modeling study on the novel designed cytotoxic quinolines. Poster session presented at the First Seminar of Medicinal & Natural Products Chemistry, Shiraz, Iran.

2004

Journal - Research Article

Loughlin, W. A., Tyndall, J. D. A., Glenn, M. P., & Fairlie, D. P. (2004). Beta-strand mimetics. Chemical Reviews, 104, 6085-6117.

Nall, T. A., Chappell, K. J., Stoermer, M. J., Fang, N.-X., Tyndall, J. D. A., Young, P. R., & Fairlie, D. P. (2004). Enzymatic characterization and homology model of a catalytically active recombinant West Nile Virus NS3 protease. Journal of Biological Chemistry, 279(47), 48535-48542.

van den Brenk, A. L., Tyndall, J. D. A., Cusack, R. M., Jones, A., Fairlie, D. P., Gahan, L. R., & Hanson, G. R. (2004). Formation of mononuclear and chloro-bridged binuclear copper(II) complexes of patellamide D, a naturally occurring cyclic peptide: Influence of anion and solvent. Journal of Inorganic Biochemistry, 98, 1857-1866.

Dutertre, S., Nicke, A., Tyndall, J. D. A., & Lewis, R. J. (2004). Determination of α-conotoxin binding modes on neuronal nicotinic acetylcholine receptors. Journal of Molecular Recognition, 17, 339-347.

March, D. R., Proctor, L. M., Stoermer, M. J., Sbaglia, R., Abbenante, G., Reid, R. C., … Tyndall, J. D. A., … Fairlie, D. P. (2004). Potent cyclic antagonists of the complement C5a receptor on human polymorphonuclear leukocytes: Relationships between structures and activity. Molecular Pharmacology, 65(4), 868-879.

Reid, R. C., Pattenden, L. K., Tyndall, J. D. A., Martin, J. L., Walsh, T., & Fairlie, D. P. (2004). Countering cooperative effects in protease inhibitors using constrained β-strand-mimicking templates in focused combinatorial libraries. Journal of Medicinal Chemistry, 47, 1641-1651.

Conference Contribution - Published proceedings: Abstract

Tyndall, J. D. A., Nall, T., Pfeiffer, B., & Fairlie, D. P. (2004). Distinctive recognition of structural motifs by proteases and GPCRS: An important principle for drug design. Proceedings of the 29th Annual Lorne Conference on Protein Structure and Function. (February). [Abstract]

Fairlie, D. P., Tyndall, J. D. A., Nall, T., Abbenante, G., & Reid, R. C. (2004). Protease ligand conformation and inhibitor design. Proceedings of the 29th Annual Lorne Conference on Protein Structure and Function. (February). [Abstract]

2003

Journal - Research Article

Milne, T. J., Abbenante, G., Tyndall, J. D. A., Halliday, J., & Lewis, R. J. (2003). Isolation and characterization of a cone snail protease with homology to CRISP proteins of the pathogenesis-related protein superfamily. Journal of Biological Chemistry, 278(33), 31105-31110.

Glenn, M. P., Kelso, M. J., Tyndall, J. D. A., & Fairlie, D. P. (2003). Conformationally homogeneous cyclic tetrapeptides: Useful new three-dimensional scaffolds. Journal of the American Chemical Society, 125(3), 640-641.

Lucke, A. J., Tyndall, J. D. A., Singh, Y., & Fairlie, D. P. (2003). Designing supramolecular structures from models of cyclic peptide scaffolds with heterocyclic constraints. Journal of Molecular Graphics & Modelling, 21, 341-355.

Hansford, K. A., Reid, R. C., Clark, C. I., Tyndall, J. D. A., Whitehouse, M. W., Guthrie, T., … Fairlie, D. P. (2003). D-tyrosine as a chiral precusor to potent inhibitors of human nonpancreatic secretory phospholipase A₂ (IIa) with antiinflammatory activity. ChemBioChem, 4(2-3), 181-185.

Conference Contribution - Published proceedings: Abstract

Milne, T. J., Abbenante, G., Tyndall, J. D. A., Halliday, J., & Lewis, R. J. (2003). Isolation and characterisation of a cone snail protease with homology to CRISP proteins of the pathogenesis-related protein superfamily. Proceedings of the 5th Australian Peptide Conference. Queensland, Australia. [Abstract]

Stoermer, M. J., March, D. R., Proctor, L. M., Sbaglia, R., Abbenante, G., Reid, R. C., … Tyndall, J. D. A., … Fairlie, D. P. (2003). Macrocyclic peptides as ligands for cellular receptors: When a little rigidity is just right... Proceedings of the Brisbane Biological and Organic Chemistry Symposium (BBOCS). (November), (pp. 17). [Abstract]

Guthrie, T., Hansford, K. A., Reid, R. C., Stoermer, M. J., Tyndall, J. D. A., & Fairlie, D. P. (2003). Isoform-selective inhibitors of human non-pancreatic secretory phospholipase A2 (group IIA): Potent new antiinfalmatory drugs derived from tyrosine. Proceedings of the Brisbane Biological and Organic Chemistry Symposium (BBOCS). (November), (pp. 39). [Abstract]

2002

Journal - Research Article

Sinchaikul, S., Tyndall, J. D. A., Fothergill-Gilmore, L. A., Taylor, P., Phutrakul, S., Chen, S.-T., & Walkinshaw, M. D. (2002). Expression, purification, crystallization and preliminary crystallographic analysis of a thermostable lipase from Bacillus stearothermophilus P1. Acta Crystallographica Section D, D58, 182-185.

Tyndall, J. D. A., Sinchaikul, S., Fothergill-Gilmore, L. A., Taylor, P., & Walkinshaw, M. D. (2002). Crystal structure of a thermostable lipase from Bacillus stearothermophilus P1. Journal of Molecular Biology, 323, 859-869.

Glenn, M. P., Pattenden, L. K., Reid, R. C., Tyssen, D. P., Tyndall, J. D. A., Birch, C. J., & Fairlie, D. P. (2002). β-strand mimicking macrocyclic amino acids: Templates for protease inhibitors with antiviral activity. Journal of Medicinal Chemistry, 45, 371-381.

Conference Contribution - Published proceedings: Abstract

Tyndall, J. D. A., Reid, R. C., Hansford, K., Clark, C., Martin, J. L., & Fairlie, D. P. (2002). Rational design and crystallographic studies of potent inhibitors of hnps-phospholipase A₂. Proceedings of the 27th Annual Lorne Conference on Protein Structure and Function. (February), (pp. B77). [Abstract]

Bond, T., Tyndall, J., Abbenante, G., Walsh, T., Halliday, J., & Lewis, R. J. (2002). Ctex31, a dibasic specific post-translational processing endoprotease isolated from Conus textile, with structural homology to the pathogenesis-related superfamily. Proceedings of the 27th Annual Lorne Conference on Protein Structure and Function. (February), (pp. B43). [Abstract]

2001

Journal - Research Article

Tyndall, J. D. A., & Fairlie, D. P. (2001). Macrocycles mimic the extended peptide conformation recognized by aspartic, serine, cysteine and metallo proteases. Current Medicinal Chemistry, 8(8), 893-907.

Conference Contribution - Poster Presentation (not in published proceedings)

Lucke, A. J., Tyndall, J. D. A., & Fairlie, D. P. (2001, November). Molecular modelling of cyclic peptide scaffolds: Designing supramolecular structures from models. Poster session presented at the Brisbane Biological and Organic Chemistry Symposium 2001, University of Queensland, Australia.

2000

Journal - Research Article

Fairlie, D. P., Tyndall, J. D. A., Reid, R. C., Wong, A. K., Abbenante, G., Scanlon, M. J., … Burkett, B. A. (2000). Conformational selection of inhibitors and substrates by proteolytic enzymes: Implications for drug design and polypeptide processing. Journal of Medicinal Chemistry, 43, 1271-1281.

Tyndall, J. D. A., Reid, R. C., Tyssen, D. P., Jardine, D. K., Todd, B., Passmore, M., … Fairlie, D. P. (2000). Synthesis, stability, antiviral activity, and protease-bound structures of substrate-mimicking constrained macrocyclic inhibitors of HIV-1 protease. Journal of Medicinal Chemistry, 43, 3495-3504.

1999

Journal - Research Article

Tyndall, J. D. A., & Fairlie, D. P. (1999). Conformational homogeneity in molecular recognition by proteolytic enzymes. Journal of Molecular Recognition, 12, 363-370.

Huang, X., Cuajungco, M. P., Atwood, C. S., Hartshorn, M. A., Tyndall, J. D. A., Hanson, G. R., … Bush, A. I. (1999). Cu(II) potentiation of Alzheimer Aβ neurotoxicity: Correlation with cell-free hydrogen peroxide production and metal reduction. Journal of Biological Chemistry, 274(52), 37111-37116.