Caren Freel Meyers

Professor @Johns Hopkins Medicine

Baltimore, MD, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Sep 2020 — Present

Professor @Johns Hopkins Medicine

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Baltimore, MD, US

APPOINTMENTS & EXPERIENCE:Johns Hopkins School of MedicineDepartment of Pharmacology and Molecular Sciences (primary)Department of Oncology (secondary)Director of Pharmacology and Molecular Sciences Graduate Training Program (since 2017)GRADUATE PROGRAMS:Pharmacology graduate programBiochemistry, Cellular and Molecular Biology graduate programChemistry-Biology Interface graduate program

EDUCATION

1999 — 2001

Purdue University

postdoctoral fellow, Organic Chemistry

2001 — 2005

Harvard Medical School

Postdoctoral Fellow, Chemical Biology

1990 — 1994

Michigan Technological University

Bachelor of Science (B.S.), Organic Chemistry

1994 — 1999

University of Rochester

Doctor of Philosophy (Ph.D.), Organic Chemistry

SKILLS

BiochemistryPharmacologyAssay DevelopmentPurificationProtein ExpressionOrganic ChemistryDrug DiscoveryOrganic SynthesisNmrMedicinal ChemistryScienceMolecular BiologyProtein ChemistryAnalytical ChemistryDrug DeliveryChemistryCancerCell BiologyFluorescence

ABOUT CAREN FREEL MEYERS

My research interests are in the areas of organic and medicinal chemistry, enzymology and drug delivery, with an emphasis on antimicrobial and anticancer drug design. ANTIMICROBIAL AGENTS: A long-term goal of my research program is to develop novel approaches to kill human pathogens, including bacterial pathogens and malaria parasites, toward development of potential therapeutic agents. Toward this goal, we are pursuing studies of bacterial isoprenoid biosynthetic enzymes comprising the methylerythritol phosphate (MEP) pathway essential in many human pathogens. Studies focus on understanding mechanism and regulation throughout the pathway toward the development of selective inhibitors of isoprenoid biosynthesis. A particular target of interest includes DXP synthase. DXP synthase catalyzes formation of DXP, a branch point metabolite feeding into isoprenoid biosynthesis as well as thiamin diphosphate and pyridoxal phosphate cofactor biosynthesis pathways critical in bacterial central metabolism. Other targets of interest include methylerythritol phosphate processing enzymes IspD, E, and F. Our strategies for creating new antimicrobials involve interdisciplinary research in the continuum of organic, biological and medicinal chemistry. DRUG DELIVERY: We are developing prodrug strategies for the intracellular delivery of highly polar phosphorylated drug molecules, including clinically-used bisphosphonates and phosphorylated inhibitors of MEP pathway enzymes, toward development of antimicrobial and anticancer therapies.

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Caren Freel Meyers — Professor at Johns Hopkins Medicine in Baltimore, MD, US | Unifers