Colorado State University NSF-REU Program in Chemistry

B. George Barisas

For more information, visit our group webpage…

            The particular focus of our research group is the motions and distribution of specific molecules on living cell surfaces and we have developed on the world's broadest collections of instrumental facilities for such measurements. Changes in these motions as various cell signaling events occur suggest functional interactions between the protein of interest and other membrane species. Despite the biological motivation for these studies, many of our people have little or no prior training in biology but come from chemistry backgrounds. Undergraduates typically select an independent project of their own but work with the assistance of a more senior group member.

            Work in our group is organized in two ways: 1) by the types of techniques being developed and 2) by the biological problem areas to which they are applied. The types of techniques we are currently developing are 1) single-particle tracking microscopy to measure diffusion of individual protein molecules on cell surfaces, 2) continuous fluorescence depletion anisotropy to measure rotation of specific cell surface proteins, 3) microscopic fluorescence lifetime apparatus to evaluate fluorescence energy transfer efficiency inside cells and 4) high intensity spot photobleaching recovery to obtain the maximum diffusion information from small numbers of fluorophores on a cell surface. Each of these methods involves developing both physical instruments and data analysis procedures. Almost everyone in the laboratory also routinely uses existing techniques of fluorescence photobleaching recovery, time-resolved phosphorescence anisotropy and photobleaching energy transfer in their work.

            The biological systems we currently study are 1) major histocompatibility complex (MHC) class II antigens involved in antigen presentation by B cells to T cells, 2) the mast cell MAFA protein which inhibits cell degranulation triggered by these cells' IgE receptors (i.e. allergic responses) and 3) the luteinizing hormone receptor on various cells involved in mammalian reproduction. All these projects involve the study of cell lines expressing structural mutants of the proteins of interest. They also involve prominent collaborators from other institutions.

Other Participating Mentors

Supported by

NSF-REU