
Professor
Biochemistry, Chemistry and the Genome Center
Davis Campus
jbsiegel@health.ucdavis.edu
The primary thrust of my research is to develop new tools and the knowledge necessary to rapidly and reliably discover novel enzyme catalysts. The projects selected have a synergy between tool and knowledge development, education, and societal impact. Research within the lab generally is focused around the use and development of computational modeling tools to evaluate how changes to a protein sequence, and therefore structure, results in a modulation of function. As members of the Rosetta Commons the majority of the modeling work carried out in the lab is done within the Rosetta Molecular Modeling Suite. We follow up the in silico modeling through in vitro studies leveraging recent breakthroughs from the field of synthetic biology to experimentally evaluate the properties of the designed proteins. On occasion we conduct in vivo studies of how the engineered proteins work within living organisms, however these studies are often done in collaboration with other groups. To date we have discovered and engineered enzymes to treat celiac disease, fight anthrax infections, catalyze novel chemistry never before observed in nature, produce high value chemicals, fixate carbon dioxide, and modulate the properties of various foods we eat.
O'Brien, T.E., S.J. Bertolani, D.J. Tantillo, and J.B. Siegel, “Mechanistically informed predictions of binding modes for carbocation intermediates of a sesquiterpene synthase reaction”. Chemical Science, 2016. 7(7): p. 4009-4015.
Carlin, D.A.*, R.W. Caster*, X. Wang, S.A. Betzenderfer, C.X. Chen, V.M. Duong, C.V. Ryklansky, A. Alpekin, N. Beaumont, H. Kapoor, N. Kim, H. Mohabbot, B. Pang, R. Teel, L. Whithaus, I. Tagkopoulos, and J.B. Siegel, “Kinetic Characterization of 100 Glycoside Hydrolase Mutants Enables the Discovery of Structural Features Correlated with Kinetic Constants”. PLoS One, 2016. 11(1): p. e0147596.
Siegel, J.B.*, A.L. Smith*, S. Poust, A.J. Wargacki, A. Bar-Even, C. Louw, B.W. Shen, C.B. Eiben, H.M. Tran, E. Noor, J.L. Gallaher, J. Bale, Y. Yoshikuni, M.H. Gelb, J.D. Keasling, B.L. Stoddard, M.E. Lidstrom, and D. Baker, “Computational protein design enables a novel one-carbon assimilation pathway”. Proc Natl Acad Sci U S A, 2015. 112(12): p. 3704-9.
Mak, W.S., S. Tran, R. Marcheschi, S. Bertolani, J. Thompson, D. Baker, J.C. Liao, and J.B. Siegel, “Integrative genomic mining for enzyme function to enable engineering of a non-natural biosynthetic pathway”. Nat Commun, 2015. 6: p. 10005.
Lucas, J.E. and J.B. Siegel, “Quantitative functional characterization of conserved molecular interactions in the active site of mannitol 2-dehydrogenase”. Protein Sci, 2015. 24(6): p. 936-45.
Harger, M.*, L. Zheng*, A. Moon, C. Ager, J.H. An, C. Choe, Y.L. Lai, B. Mo, D. Zong, M.D. Smith, R.G. Egbert, J.H. Mills, D. Baker, I.S. Pultz, and J.B. Siegel, “Expanding the product profile of a microbial alkane biosynthetic pathway”. ACS Synth Biol, 2013. 2(1): p. 59-62.
Gordon, S.R.*, E.J. Stanley*, S. Wolf, A. Toland, S.J. Wu, D. Hadidi, J.H. Mills, D. Baker, I.S. Pultz, and J.B. Siegel, “Computational design of an alpha-gliadin peptidase”. J Am Chem Soc, 2012. 134(50): p. 20513-20.
Eiben, C.B.*, J.B. Siegel*, J.B. Bale, S. Cooper, F. Khatib, B.W. Shen, F. Players, B.L. Stoddard, Z. Popovic, and D. Baker, “Increased Diels-Alderase activity through backbone remodeling guided by Foldit players”. Nat Biotechnol, 2012. 30(2): p. 190-2.
Wu, S.J., C.B. Eiben, J.H. Carra, I. Huang, D. Zong, P. Liu, C.T. Wu, J. Nivala, J. Dunbar, T. Huber, J. Senft, R. Schokman, M.D. Smith, J.H. Mills, A.M. Friedlander, D. Baker, and J.B. Siegel, “Improvement of a Potential Anthrax Therapeutic by Computational Protein Design”. Journal of Biological Chemistry, 2011. 286(37): p. 32586-32592.
Siegel, J.B.*, A. Zanghellini*, H.M. Lovick, G. Kiss, A.R. Lambert, J.L. St Clair, J.L. Gallaher, D. Hilvert, M.H. Gelb, B.L. Stoddard, K.N. Houk, F.E. Michael, and D. Baker, “Computational design of an enzyme catalyst for a stereoselective bimolecular Diels-Alder reaction”. Science, 2010. 329(5989): p. 309-13.