Jon Clardy

Jon Clardy (born May 16, 1943, Washington, D.C., United States) is currently the Hsien Wu and Daisy Yen Wu professor of biological chemistry and molecular pharmacology at Harvard Medical School.[1] His research focuses on the isolation and structural characterization of natural products, and currently investigates the role of biologically active small molecules in mediating symbiotic interactions and disease.[2]

Biography

Clardy grew up in Arlington, Virginia, United States, the oldest of four children. He attended Yale University where he received a B.S. in 1964 and was elected to Phi Beta Kappa. While he was always captivated by biology, during college he became more interested in chemistry. He performed undergraduate research in organic synthesis, with an emphasis on benzyne.[3] After graduating from Yale, he moved to Harvard University, where he received a Ph.D. in chemistry in 1969. He then accepted a faculty position in the Chemistry Department at Iowa State University, where he was affiliated with the Ames Laboratory. In 1978, he moved to the Chemistry Department at Cornell University where he stayed until 2002, when he moved to the Biological Chemistry and Molecular Pharmacology Department at Harvard Medical School. In 2004, he started the Ph.D. Program in Chemical Biology with Stuart Schreiber and Greg Verdine.[4] He also created, and continues to teach, a popular class entitled “Molecules of Life” for Harvard undergraduates who are not majoring in sciences.

While pursuing his Ph.D., Clardy met his wife Andrea Fleck, a Swarthmore College graduate, who is a writer. Her works include a children’s book, two books about upstate New York, and plays that have been performed across the country. They have two sons.

Natural product discovery

Clardy’s early research focused on the structure elucidation of natural products primarily by x-ray crystallography. Early on at Iowa State University Clardy established important collaborations with Bill Fenical, John Faulkner and Paul Scheuer,[5] which led to the structure elucidation of numerous marine natural products such as the anticancer agent bryostatin,[6] the insecticidal and antifungal jaspamide, diazonamide A and B,[7] and many others. Some of his most notable early work focused on the neurotoxins associated with “red tide” – which led to the determination of the three dimensional structures of saxitoxin,[8] of the gonyautoxin group, and the cyclic polyether brevetoxin B.[9] Upon moving to Cornell University, Clardy’s research expanded to include a huge variety of non-marine organisms including, but not limited to, fungi, Actinobacteria and C. elegans. His longstanding interest in endophytic fungi led to the discovery of the selectively cytotoxic quinone torreyanic acid, the structurally diverse guanacastepenes, the antimycotic agent cryptocin, and many others.

Recently, Clardy has focused on symbiotic associations between bacteria and other organisms as rich sources of novel small molecules.[10] In collaboration with Cameron Currie, Clardy investigated associations between Actinomycetes and insects such as the southern pine beetle, ants and termites that led to the discovery of antifungal agents including dentigerumycin[11][12] and mycangimycin.[13][14] The study of chemical exchange in complex ecological interactions remains a central focus of the Clardy lab.[15]

X-ray crystallography of small molecule – protein interactions

Clardy, in collaboration with Stuart Schreiber and colleagues, obtained the crystal structure for both the FK506/FKBP12 and rapamycin/FKBP12 complexes.[16] Shortly thereafter Schreiber and Clardy went on to determine the structure of the FK506/rapamycin/FRAP complex – a groundbreaking study that revealed the ability of a cell-permeable small molecule to facilitate protein dimerization.[17] Vertex, a start-up pharmaceutical company, was founded to design a nontoxic version of FK506.[18] In collaboration with Walter Leal, Clardy and colleagues obtained an x-ray crystal structure for the volatile insect pheromone bombykol with its binding partner located on the antennae of female silkworm moths.[19] Besides further enhancing the understanding of this highly specific small-molecule-protein interaction, this study marked the first three-dimensional structure of an odorant-binding protein.[20]

eDNA

Clardy is also known for his work in elucidating natural products made by unculturable bacteria and is credited, along with Jo Handelsman and Robert M. Goodman, for pioneering the field of metagenomics. With Sean Brady, he developed a method to insert DNA directly from environmental DNA (eDNA) like soil, into cosmid libraries, search for biosynthetic gene clusters and identify the products of these genes.[21] Using this method they elucidated the structures of numerous antibiotics previously unattainable by traditional lab techniques, such as natural products derived from long-chain N-acyltyrosines.[22]

References

  1. ↑ "BCMP | Department of Biological Chemistry & Molecular Pharmacology". Bcmp.med.harvard.edu. Retrieved 2013-09-28.
  2. ↑ "Jon Clardy | Clardy Laboratory". Clardy.med.harvard.edu. Retrieved 2013-09-28.
  3. ↑ Berry, R. S., Clardy, J. & Schafer, M. E. Benzyne. J. Am. Chem. Soc. 86, 2738–2739 (1964)
  4. ↑ "The Chemical Biologists | Harvard Magazine Mar-Apr 2005". Harvardmagazine.com. Retrieved 2013-09-28.
  5. ↑ The American Society of Pharmacognosy Newsletter. 1-3 (2004)
  6. ↑ Pettit, G. R. et al. Isolation and structure of bryostatin 1. J. Am. Chem. Soc. 104, 6846–6848 (1982)
  7. ↑ Lindquist, N., Fenical, W., Van Duyne, G. D. & Clardy, J. Isolation and structure determination of diazonamides A and B, unusual cytotoxic metabolites from the marine ascidian Diazona chinensis. J. Am. Chem. Soc. 113, 2303–2304 (1991)
  8. ↑ Schantz, E. J. et al. Structure of saxitoxin. J. Am. Chem. Soc. 97, 1238–1239 (1975)
  9. ↑ Lin, Y.-Y. et al. Isolation and structure of brevetoxin B from the‘ red tide’ dinoflagellate Ptychodiscus brevis (Gymnodinium breve). J. Am. Chem. Soc. 103, 6773–6775 (1981)
  10. ↑ "Of beetles and bacteria | The Scientist Magazine®". web.archive.org. Retrieved 2014-08-25.
  11. ↑ Oh, D.-C., Poulsen, M., Currie, C. R. & Clardy, J. Dentigerumycin: a bacterial mediator of an ant-fungus symbiosis. Nat Chem Biol 5, 391–393 (2009)
  12. ↑ Willson, E. & Yarnell, A. In Cahoots: Fungi, Ants, And Bacteria. C&EN News 87, 15 (2009)
  13. ↑ Scott, J. J. et al. Bacterial protection of beetle-fungus mutualism. Science 322, 63 (2008)
  14. ↑ Drahl, C. Beetle Bacteria Wield An Antifungal Agent. C&EN News 86, 47 (2008)
  15. ↑ "Jon Clardy". Academy.asm.org. Retrieved 2013-09-28.
  16. ↑ Van Duyne, G.D., Standaert, R. F., Karplus, P. A., Schreiber. S.L., Clardy J. Atomic structure of FKBP-FK506, an immunophilin-immunosuppressant complex. Science 252, 839-842 (1991)
  17. ↑ Choi, J., Chen, J., Schreiber S. L., Clardy J. Structure of the FKBP12-rapamycin complex interacting with the binding domain of human FRAP. Science 273, 239-242 (1996)
  18. ↑ Billion Dollar Molecule: The Quest for the Perfect Drug, Barry Werth, 1994
  19. ↑ Sandler, B. H., Nikonova, L., Leal, W. S. & Clardy, J. Sexual attraction in the silkworm moth: structure of the pheromone-binding-protein-bombykol complex. Chemistry & Biology 7, 143–151 (2000)
  20. ↑ Sandler, B. H., Nikonova, L., Leal, W. S. & Clardy, J. Sexual attraction in the silkworm moth: structure of the pheromone-binding-protein–bombykol complex. Chemistry & Biology 7, 143–151 (2000)
  21. ↑ Brady, S. F., Chao, C. J. & Clardy, J. New Natural Product Families from an Environmental DNA (eDNA) Gene Cluster. J. Am. Chem. Soc. 124, 9968–9969 (2002)
  22. ↑ Brady, S. F., Chao, C. J. & Clardy, J. Long-chain N-acyltyrosine synthases from environmental DNA. Appl. Environ. Microbiol. 70, 6865–6870 (2004)
This article is issued from Wikipedia - version of the Sunday, August 23, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.