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
Phaeosphaeride A, an inhibitor of STAT3-dependent signaling isolated from an endophytic fungus.
Authors: Authors: Maloney KN, Hao W, Xu J, Gibbons J, Hucul J, Roll D, Brady SF, Schroeder FC, Clardy J.
Org Lett
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A biosynthetic gene cluster for the acetyl-CoA carboxylase inhibitor andrimid.
Authors: Authors: Jin M, Fischbach MA, Clardy J.
J Am Chem Soc
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Human methionine aminopeptidase type 2 in complex with L- and D-methionine.
Authors: Authors: Nonato MC, Widom J, Clardy J.
Bioorg Med Chem Lett
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Brequinar derivatives and species-specific drug design for dihydroorotate dehydrogenase.
Authors: Authors: Hurt DE, Sutton AE, Clardy J.
Bioorg Med Chem Lett
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Structure of Plasmodium falciparum dihydroorotate dehydrogenase with a bound inhibitor.
Authors: Authors: Hurt DE, Widom J, Clardy J.
Acta Crystallogr D Biol Crystallogr
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Isolation and structure assignment of an iminotetrasaccharide from a cultured filamentous cyanobacterium Anabaena sp.
Authors: Authors: Thammana S, Suzuki H, Lobkovsky E, Clardy J, Shimizu Y.
J Nat Prod
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Stopping trouble before it starts.
Authors: Authors: Clardy J.
ACS Chem Biol
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Systematic investigation of the Escherichia coli metabolome for the biosynthetic origin of an isocyanide carbon atom.
Authors: Authors: Brady SF, Clardy J.
Angew Chem Int Ed Engl
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Cloning and heterologous expression of isocyanide biosynthetic genes from environmental DNA.
Authors: Authors: Brady SF, Clardy J.
Angew Chem Int Ed Engl
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Coil-to-helix transition and ligand release of Bombyx mori pheromone-binding protein.
Authors: Authors: Lautenschlager C, Leal WS, Clardy J.
Biochem Biophys Res Commun
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