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Paul Sternweis

 
 
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Paul Sternweis, Ph.D.

 Details of Research

Biographical Sketch Details of Research Personal Overview How to Contact
Paul Sternweis
Name:
  Paul Charles Sternweis, Ph.D.
Endowed Title:
  Alfred and Mabel Gilman Chair in Molecular Pharmacology
Academic Title:
  Professor
Primary Appointment:
  Pharmacology
School:
  Graduate School of Biomedical Sciences
Southwestern Medical School
Degree Program:
  Cell Regulation
Department Website:
  Department of Pharmacology
Email:
  Paul Sternweis, Ph.D.

 RESEARCH OVERVIEW
 
A major area of research explores signaling pathways that utilize cell surface receptors and membrane associated GTP-binding proteins (G proteins). These G proteins mediate hormonal regulation of intracellular enzymes, which produce various second messengers and their sequelae. Examples of G protein regulated systems include production of cAMP and several lipid-derived second messengers such as the phosphoinositides. In addition, the G proteins can more directly regulate a variety of signaling proteins such as ion channels, protein kinases and exchange factors for other GTPases. Major goals have been identification of the participants in these pathways, elucidation of the circuitry which defines interaction among the various components and definition of the molecular mechanisms by which regulation is achieved.

A specific focus in this area has been the mechanisms for regulation of guanine nucleotide exchange factors for RhoA (RhoGEFs) by the heterotrimeric G12 and G13 proteins. This finding represents the first direct regulatory link between the receptor coupled G proteins and the monomeric GTPases. Besides the hormonal regulation of Rho-dependent cytoskeletal regulation and gene transcription, this pathway offers a unique paradigm for regulation in that the RhoGEF acts bi-directionally as both a recipient for activation by the G proteins as well as a facilitator of inactivation of the G proteins. Current studies focus on elucidating the mechanisms of these regulatory actions, determining their in vivo relevance and discovery of other similar regulatory paradigms that link G protein coupled receptors to the monomeric GTPases. This is being accomplished through the pursuit of traditional biochemical approaches, determination of molecular structures for the individual proteins and their active complexes, development of fluorescent biosensors to detect the activated states of pathway components in vivo, and selective perturbation of specific pathway components to assess physiological impact.

A second focus, in collaboration with Li Jiang at UT-Southwestern, is the elucidation of interacting G protein pathways that regulate cAMP in macrophages. In these cells, all four major G proteins intersect to synergistically modulate the activity of a specific adenylyl cyclase isoform, AC7. Efforts are directed at determining the molecular mechanisms of this synergistic regulation and the role of this specific cyclase in the immune system. Approaches include direct biochemical dissection of the system and physiolgical characterization of mice lacking AC7.
 
 RESEARCH INTERESTS
 
Integration of Hormone Signaling Pathways
Mechanisms of G protein-mediated Signaling
Structures of Signaling Molecules
Regulation of Rho GTPases
Fluorescent Sensors to measure in vivo activities
 
 RECENT PUBLICATIONS
 
Chen, Z, Singer, W.D., Danesh, S.M., Sternweis, P.C., Sprang, S.R., "Recognition of the Activated States of Galpha13 by the rgRGS Domain of PDZRhoGEF" Structure, 16:1532-1543, October 2008
Jiang, L.I., Collins, J., Davis, R., Fraser, I.D., Sternweis, P.C., "Regulation of cAMP responses by the G12/13 pathway converges on adenylyl cyclase VII." J. Biol. Chem., 283:23429-39, August 2008
Sternweis, P.C., Carter, A.M., Chen, Z., Danesh, S.M., Hsuing, Y.F., Singer, W.D., "Regulation of Rho guanine nucleotide exchange factors by G proteins" Adv. Protein Chem., 74:189-228, 2007
Jiang, L.I., Collins, J., Davis, R., Lin, K-M., DeCamp, D., Roach, T., Hsueh, R., Rebres, R.A., Ross, E.M., Taussig, R., Fraser, I., Sternweis, PC., "Use of a cAMP BRET sensor to characterize a novel regulation of cAMP by the sphingosine 1-phosphate/G13 pathway." J. Biol. Chem., 282:10576-84, April 2007
Chen, Z., Singer, W.D., Sternweis, P.C., Sprang, S.R., "Structure of the p115RhoGEF rgRGS domain-Galpha13/i1 chimera complex suggests convergent evolution of a GTPase activator." Nat. Struct. Mol. Biol., 12:191-7, February 2005
 
 SIGNIFICANT PUBLICATIONS
 
Hart, M.J., Jiang, X., Kozasa, T., Roscoe, W., Singer, W.D., Gilman, A.G., Sternweis, P.C., and Bollag, G., "Direct Stimulation of the Guanine Nucleotide Exchange Activity of p115 RhoGEF by Ga13." Science, 280:2112-2114, 1998
Kozasa, T., Jiang, X., Hart, M.J., Sternweis, P.M., Singer, W.D., Gilman, A.G., Bollag, G. and Sternweis, P.C., "p115 RhoGEF, a GTPase Activating Protein for Ga12 and Ga13." Science, 280:2109-2111, 1998
Natarajan, M., Lin, K-M., Hsueh, R.C., Sternweis, P.C., Ranganathan, R., "A global analysis of cross-talk in a mammalian cellular signalling network." Nat. Cell Biol., 8:571-80, June 2006
 
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