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Education

 B.S. in Biochemistry from California State University of Los Angeles in 1971

Ph.D. in Biochemistry from the University of Wisconsin, Madison in 1977

Postdoctoral studies with Robert Fletterick at the University of Alberta and the University of California at San Francisco, 1978-1983

Research Interests

 Current work focuses on mechanisms of G protein activation by an intracellular guanine nucleotide exchange factor called Ric-8A. This protein appears to carry out multiple functions in cells: it is essential for asymmetric cell division and abscission, regulates neurotransmitter secretion and assists in the biogenesis of G protein alpha subunits, in addition to its role as a G protein activator. Ric-8A functions as a guanine nucleotide exchange factor by catalyzing the release of GDP from G alpha subunits. Ric-8A forms a nucleotide-free complex with G alpha, which dissociates only in the presence of GTP, leading to the formation of active GTP-bound alpha. In this regard, Ric-8A is functionally analogous to the well-characterized family of trans-membrane G Protein-Coupled Receptors (GPCR), which, upon agonist binding, catalyze nucleotide exchange from G protein heterotrimers.

We have shown that Ric-8A catalyzes nucleotide exchange by inducing large conformational changes within G alpha, possibly by inducing local unfolding at the nucleotide binding site and in surrounding elements of secondary structure. In analogy to the action of GPCRs, Ric-8A also induces separation of the two major domains of G alpha. We have employed a variety of biophysical methods to characterize Ric-8A-induced structural changes in G alpha, including scanning calorimetry, Double Electron-Electron spectroscopy (in collaboration with Wayne Hubbell's laboratory at UCLA), Hydrogen-Deuterium Mass Spectrometry (in collaboration with Brian Bothner's group at Montana State University), single-molecule fluorescence spectroscopy (with Sandy Ross at ÀÏ»¢»ú¹¥ÂÔ), and most recently using camelid nanobodies as functional and structural probes (in collaboration with Jan Staeyert's laboratory at VIB, the Netherlands). We make extensive use of site-directed mutagenesis, in conjunction with enzymological methods to understand the mechanism of Ric-8A action. Our laboratory studies other aspects of G protein function, as described in our publications, as well as the mechanism of adenylyl cyclase regulation.

Our work is funded by grants from the National Institutes of Health (R01GM105993)

Projects

I am retired from my administrative duties as director of the (2007 - 2020) and as a faculty member of the Division of Biological Sciences.  As such, I no longer mentor graduate students or postdoctoral trainees.  As a part-time research project, I explore the kinetics and specificity catalytic activity of Ric-8A on G proteins and in the Integrated Structural Biology core and assist its staff in various tasks.  The general theme of the research that my laboratory has conducted over the past ten years is described below.

Field of Study

Structural Biology and Biochemistry: Biological Signal Transduction

Selected Publications

Maziarz M, Leyme A, Marivin A, Luebbers A, Patel PP, Chen Z, Sprang SR, Garcia-Marcos M.J Biol Chem. 2018 Dec 21;293(51):19586-19599. doi: 10.1074/jbc.RA118.005291. Epub 2018 Oct 23.PMID:30352874

Kant R, Zeng B, Thomas, CJ, Bothner, B, Sprang SR (2016) "" eLife. Elife. 2016 Dec 23;5. pii: e19238. doi: 10.7554/eLife.19238

Black LA, Thomas CJ, Nix GN, Terwilliger MC, Sprang SR, Ross JBA. "" Biophys J. 2016 Aug 23;111(4):722-731. doi: 10.1016/j.bpj.2016.07.021.

Sprang SR Biopolymers. 2016 Aug;105(8):449-62. doi: 10.1002/bip.22836. Review. PMID: 26996924

Van Eps N, Thomas CJ, Hubbell WL, Sprang SR. (2015) "The guanine nucleotide exchange factor Ric-8A induces domain separation and Ras domain plasticity in Galphai1" Proc Natl Acad Sci U S A. 2015 Feb 3;112(5):1404-9. doi: 10.1073/pnas.1423878112. Epub 2015 Jan 20.

Chan P, Thomas CJ, Sprang SR, Tall GG. (2013) Molecular chaperoning function of Ric-8A is to fold nascent heterotrimeric G protein alpha subunits". Proc Natl Acad Sci U S A. 2013 Mar 5;110(10):3794-9. doi: 10.1073/pnas.1220943110. Epub 2013 Feb 19.PMID:23431197[PubMed - indexed for MEDLINE]

Thomas CJ, Briknarová K, Hilmer JK, Movahed N, Bothner B, Sumida JP, Tall GG, Sprang SR.(2011) "The nucleotide exchange factor Ric-8A is a chaperone for the conformationally dynamics nucleotide-free state of Galphai1" PLoS One. 2011;6(8):e23197. doi: 10.1371/journal.pone.0023197. Epub 2011 Aug 11.PMID:21853086[PubMed - indexed for MEDLINE]

Thomas, CJ, Tall, GG, Adhikari, A, Sprang, SR (2008) "Ric-8A catalyzes guanine nucleotide exchange on Galphai1 bound to the GPC/GoLoco exchange inhibitor AGS3" J. Biol. Chem., 283, 23150-60

Chen, Z., Singer, WD,  Danesh, SM, Sternweis, PC, Sprang, SR (2008) "Recognition of the activated states of Galpha13 by the rgRGS domain of PDZRhoGEF, Structure, 16, 1532-43

Sprang, S.R., Chen, Z and Du, X. (2007)“Structural basis of effector regulation and signal termination in heterotrimeric Ga proteins” Advances Prot. Chem. 74:1-65

Davis, T.,  Bonacci, T.M., Smrcka, AV. and Sprang, S.R. (2005) “Structural and Molecular Characterization  of a Preferred Protein Interaction Surface on G Protein bg Subunits” (2005) Biochemistry 44:10593-10604

Chen, Z., Singer, W.D., Sternweis, P.C. and Sprang, S. R. “Structure of the p115rhoGEF rgRGS domain of-Ga1/i1 chimera complex suggests convergent evolution of a GTPase activator “ (2005), Nature Structural and Molecular Biology, 12:191-7

Mou, T.C., Gille, A., Fancy, DA, Seifert, R and Sprang, S.R.,  (2005) “Structural basis for the inhibition of mammalian adenylyl cyclase by 2’(3’)-O-(N-methylanthraniolyl)-guanosine 5’-triphosphate”  Journal of Biololgical Chemistry, 280:7253-61

 Chen, Z., Singer, W.D., Sternweis, P.C. and Sprang, S. R. “Structure of the p115rhoGEF rgRGS domain of-Ga1/i1 chimera complex suggests convergent evolution of a GTPase activator “ (2005), Nature Structural and Molecular Biology, 12:191-7

Xiao, T, Towb P., Wasserman, S.A. and Sprang, S.R. (1999) Three-Dimensional Structure of a Complex between the Death Domains of Pelle and Tube. Cell 99: 545-555.

Tesmer, J.J.G., Sunahara, R.K., Johnson, R.A., Gosselin G., Gilman, A.G., and Sprang, S.R (1999) Two metal ion catalysis in adenylyl cyclase revealed by its complexes with ATP analogs, Mg2+, Mn2+ and Zn2+. Science 285:756-760.

Tesmer, J. J. G., Sunahara, R. K., Gilman, A. G. and Sprang, S. R. (1997).  Crystal structure of the catalytic domains of adenylyl cyclase in a complex with Gsa•GTPgS. Science 278:1907-1916

Sprang, S. R. (1997).  G Protein Mechanisms: Insights from structural analysis. Annual Review of Biochememistry 66:639-678.

Tesmer, J. J. G., Berman, D. M., Gilman, A. G. and Sprang, S. R. (1997).  Structure of RGS4 bound to AIF4-- activated Gia1: Stabilization of the transition state for GTP hydrolysis.  Cell 89:251-261

Wall, M. A., Coleman, D. E., Lee, E., Iñiguez-Lluhi, J. A., Posner, B. A., Gilman, A. G. and Sprang, S. R. (1995).  The structure of the G protein heterotrimer Giab1g2. Cell 80:1047-105

Sutton, R. B., Davletov, B.A., Berghuis, A. M., Südhof, T. C. and Sprang, S. R. (1995).Structure of the first C2-domain of synaptotagmin I: A novel Ca2+/phospholipid binding fold.  Cell 80:929-938

Naismith, J. H., Devine, T. Q., Brandhuber, B. J. and Sprang, S. R. (1995).  Crystallographic evidence for dimerization of unliganded tumor necrosis factor receptor.  Journal of Biological Chemistry 270:13303-13307.

Coleman, D. E.,  Berghuis, A., Lee, E., Gilman, A. and Sprang, S. (1994). Structures of active conformations of Gia1 and the mechanism of GTP hydrolysis.  Science 265:1405-1412.

Publications

Affiliations

American Chemical Society

Biophysical Society

Honors / Awards

Fellow of the American Association for the Advancement of Science, 2000