Picture of Jon Clardy

Jon Clardy, Ph.D.

Christopher T. Walsh Professor of Biological Chemistry and Molecular Pharmacology

The laboratory focuses on biologically active small molecules, especially those from bacteria and fungi with an overall goal of understanding how small molecules control biological processes. 

Research:

The laboratory focuses on biologically active small molecules, especially those from bacteria and fungi with an overall goal of understanding how small molecules control biological processes.  Organizing themes include: 1) function-based discovery of microbially-produced small molecules and their roles in microbial symbioses , 2) function-based discovery of biologically active small molecules using high-throughput screening,  3) genome-based discovery of bacterially-produced small molecules. 

1.  We have focused on the small molecule exchanges that underlie multilateral symbioses involving bacteria, partly because they are widespread and poorly understood and partly because they lead to the discovery of new useful molecules in the biological context in which they evolved.  Current projects involve the bacterial symbionts of fungus-growing ants, members of the human gut microbiome linked to disease, and interactions between micro-algae and bacteria.

2.  We also continue to discover small molecules in a more medically relevant context: high-throughput screening for a variety of diseases.  In these projects we have focused on antibacterial, antifungal, and antiparasitic agents along with immunomodulators and anticancer agents. 

3.  It is now quite clear that well studied bacteria – the producers of drugs that are used on the ton scale, for example – are genetically capable of producing many more potentially useful small molecules.  The biosynthetic gene can be seen but the associated molecules have never been characterized.  Ways to access these cryptic metabolites is a current focus of the laboratory.

Address: 

Room C-643

240 Longwood Avenue

Boston, MA 02115

Publications View
Atlas for drug discovery.
Authors: Authors: Stallforth P, Clardy J.
Proc Natl Acad Sci U S A
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Dihydroquinazolinone inhibitors of proliferation of blood and liver stage malaria parasites.
Authors: Authors: Derbyshire ER, Min J, Guiguemde WA, Clark JA, Connelly MC, Magalhães AD, Guy RK, Clardy J.
Antimicrob Agents Chemother
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Bacterial symbionts in agricultural systems provide a strategic source for antibiotic discovery.
Authors: Authors: Ramadhar TR, Beemelmanns C, Currie CR, Clardy J.
J Antibiot (Tokyo)
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A bacterial symbiont is converted from an inedible producer of beneficial molecules into food by a single mutation in the gacA gene.
Authors: Authors: Stallforth P, Brock DA, Cantley AM, Tian X, Queller DC, Strassmann JE, Clardy J.
Proc Natl Acad Sci U S A
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Pharbinilic acid, an allogibberic acid from morning glory (Pharbitis nil).
Authors: Authors: Kim KH, Choi SU, Son MW, Choi SZ, Clardy J, Lee KR.
J Nat Prod
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Closing in on a new treatment for sleeping sickness.
Authors: Authors: Derbyshire ER, Clardy J.
Elife
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Production of a-galactosylceramide by a prominent member of the human gut microbiota.
Authors: Authors: Wieland Brown LC, Penaranda C, Kashyap PC, Williams BB, Clardy J, Kronenberg M, Sonnenburg JL, Comstock LE, Bluestone JA, Fischbach MA.
PLoS Biol
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X-ray crystallography: One size fits most.
Authors: Authors: Stallforth P, Clardy J.
Nature
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1,2,3,4,6-Penta-O-galloyl-ß-D-glucopyranose inhibits angiogenesis via inhibition of capillary morphogenesis gene 2.
Authors: Authors: Cryan LM, Bazinet L, Habeshian KA, Cao S, Clardy J, Christensen KA, Rogers MS.
J Med Chem
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Synthesis and activity of biomimetic biofilm disruptors.
Authors: Authors: Böttcher T, Kolodkin-Gal I, Kolter R, Losick R, Clardy J.
J Am Chem Soc
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