Office for the Promotion of Women in Science, Engineering, and Mathematics
Faculty Profile
Storch, Judith
Judith's Profile
Storch, Judith

Phone: 732-932-1689

Ph.D., Columbia University, 1983

Professional Summary/CV [.PDF]

Department of Nutritional Sciences, School of Environmental and Biological Sciences, New Brunswick; Rutgers
Areas of Interest
Lipid binding proteins, Intestinal lipid absorption, metabolism and transport, Membrane-protein interactions, Intracellular fatty acid and cholesterol trafficking.

Teaching Areas
Advanced Nutrition, Obesity and Biology, Nutritional Aspects of Disease.
Memberships and Professional Service
Member of American Society for Nutrition, American Society for Biochemistry and Molecular Biology, American Association for Advancement of Science, Sigma Xi Scientific Research Society; Member of Nutritional Sciences Council, American Society for Nutrition, 2006-2009; Member of Finance Committee, American Society for Nutrition, 2004-2007; Editorial Board, Journal of Biological Chemistry, 2003-2008, Editorial Board, Biochim Biophys Acta Lipids, 2007-2010.
Grants, Honors, and Awards
Principal Investigator, National Institutes of Health, "Fatty Acid Transport in the Intestine," 1987-2008; Principal Investigator, National Institutes of Health, "Liquid Chromatography Mass Spectrometry System," 2006-2007; Principal Investigator, Johnson and Johnson Discovery Award, “Alpha-glycoprotein and chronic disease,” 2006-2008; Sustained Research Excellence Award, Rutgers School of Environmental and Biological Sciences, 2007.
Academic Interests and Plans
The overall focus of research my laboratory is on lipid traffic in cells, with particular emphasis on long-chain fatty acids, monoacylglycerols, and cholesterol. My laboratory uses a combination of biochemical, biophysical, cell and molecular biological approaches to answer these questions. For example, fluorescence spectroscopic analysis of recombinant FABP is used to examine the interactions of fatty acids with FABP and the kinetics of fatty acid and monoacylglycerol transfer between FABP and membranes. The structural determinants of ligand-protein interactions and FABP-membrane interactions are probed using chemical modification and site-directed mutagenesis. Cell culture systems such as the Caco-2 human intestinal cell line and 3T3-L1 adipocytes are used to examine cellular lipid transport using biochemical methods and confocal microscopy. The functions of FABPs are also studied using transgenic mouse models in which specific FABP expression has been "knocked out" and in cultured cells by manipulation of FABP content. The metabolic polarity of fatty acid and monoacylglycerol in the intestinal cell is studied using a variety of mouse models and cell culture approaches. Human fibroblasts from patients with NPC disease are used to examine the function of the NPC2 protein in cholesterol trafficking. These studies are providing fundamental information about the cellular trafficking of lipids, with the ultimate goal of enabling effective preventive and therapeutic approaches to a variety of pathologic conditions including obesity, cardiovascular disease, and lipid-storage diseases.