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Top blue bar image Department of Biochemistry & Cell Biology
 

Jonathan Silberg

Associate Professor of Biochemistry and Cell Biology

The objective of our group is to elucidate and manipulate the functions of proteins. Our biochemical research is focused on: silberg_figure (i) investigating if a protein’s mutational tolerance reports on its functionally important motions, (ii) using structure-guided protein recombination to understand sequence-structure-function relationships within protein complexes, and (iii) understanding the regulation Fe-S cluster biosynthesis. Our synthetic biology research is focused on: (iv) developing new methods for laboratory evolution that accelerate our ability to overcome component limitations, (v) building new enzyme technologies for increasing spatial and temporal control over metabolic labeling, and (vi) establishing reporters for biosensing in hard-to-image conditions, e.g., animals, biochars, and soils. Our expertise in biochemistry and biomolecular design puts us in a unique position to study living systems, as we take advantage of classical methods for biochemical inquiry and develop and apply novel biotechnologies to support these lines of research. Our philosophy is that transformative advances occur when biochemical studies are extended to conditions that reflect those within living cells and the environment, and important synthetic biology advances occur when experimental observations can be anticipated using physical models.

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Mahdavi, A., Segall-Shapiro, T.H., Kou, S., Jindal, G.A., Hoff, K.G., Liu, S., Chitsaz, M., Ismagilov, J.J., Silberg, J.J., and Tirrell, D.A. A genetic AND gate for selective interrogation of cellular protein synthesis.  JACS, 135 2013: 2979-2982

Masiello, C.A., Ye, C., Gao, G., Liu, S., Cheng, H.Y., Bennett, M.R., Rudgers, J.A., Wagner, D.S., Zygourakis, K., and Silberg, J.J. Biochar and microbial signaling: production conditions determine effects on microbial communication.  Environ. Sci. Technol. , 47 2013: 11496-11503

LeCroy, C., Masiello, C.A., Rudgers, J.A., Hockaday, W.C., and Silberg, J.J. Nitrogen, biochar, and mycorrhizae: Alteration of the symbiosis and oxidation of the char surface.  Soil Biology and Biochemistry, 58 2013: 248-254

Ho, M.L., Adler, B., Torre, M., Silberg, J.J., and Suh, J. SCHEMA computational design of virus capsid chimeras: calibrating how DNA packaging, protection, and transduction correlate with calculated disruption.  ACS Synth. Biol., 2 2013: 724-733

Zhao, W., Bonem, M., McWhite, C., Silberg, J.J., and Segatori, L. The Deg-On system: a mammalian synthetic gene circuit to quantify proteasomal degradation.  in review 2013

Judd, J., Ho, M.L., Tiwari, A., Gomez, E.J., Dempsey, C., Van Vliet, K., Igoshin, O., Silberg, J.J., Agbandje-McKenna, M., and Suh, J. Tunable virus nanonodes programmed to compute proteolytic signatures.  in review 2013

Mehta, M, Liu, S., and Silberg, J.J. A transposase strategy for creating libraries of circularly permuted proteins.  Nucleic Acids Research, 40(9) 2012: e71

Judd, J., Wei, F., Nguyen, P.Q., Tartaglia, L. J., Agbandje-McKenna, M., Silberg, J.J., and Suh, J. Random insertion of mCherry into the VP3 domain of adeno-associated virus (AAV) yields fluorescent capsids with no loss of infectivity.  Molecular Therapy – Nucleic Acids, 1 2012: e1

Vu, M, Zhai, P., Lee, J, Guerra, C., Liu, S., Gustin, M.C., and Silberg, J.J. The DNLZ/HEP zinc-binding domain is critical for regulation of the mitochondrial chaperone HSPA9.  Protein Science, 21 2012: 258-267

Zhai, P., Vu, M.T., Hoff, K.G., and Silberg, J.J. A conserved histidine in human DNLZ/HEP is required for stimulation of HSPA9 ATPase activity.  Biochem. Biophys. Res. Comm. , 408 2011: 589-594

Segall-Shapiro, T.H., Nguyen, P.Q., Dos Santos, E., Subedi, S., Suh, J., and Silberg, J.J. Mesophilic and hyperthermophilic adenylate kinases differ in their tolerance to random fragmentation.  J. Mol. Biol., 406 2011: 135-148

McGuire, R.M., Silberg, J.J., Pereira, F.A., and Raphael, R.M. Selective cell-surface labeling of the molecular motor prestin.  Biochem. Biophys. Res. Comm. , 410 2011: 134-139

Nguyen, P.Q. and Silberg, J.J. A selection for detecting protein-protein interactions within a thermophilic bacterium.  Prot. Eng. Des. & Sel., 23 2010: 529-536

Silberg, J.J., Nguyen, P.Q., and Stevenson, T. Computational design of chimeric protein libraries for directed evolution.  Methods in Molecular Biology: Topics in Computational Biology , 673 2010: 175-188

Hoff, K.G., Li, R., Goodlitt, R., Smolke, C. D., and Silberg, J.J., Fluorescence detection of protein-bound 2Fe2S clusters.  ChemBioChem, 10 2009: 667-670

Hoff, K.G., Culler, S. J., Nguyen, P. Q., McGuire, R.M., Silberg, J. J., and Smolke, C. D. In vivo fluorescent detection of Fe-S clusters coordinated by human GRX2.  Chemistry & Biology, 16 2009: 1299-1308

Silberg, J.J., and Nguyen, P.Q. Models predicting optimized strategies for protein evolution.  The Metabolic Pathway Engineering Handbook , 2 2009

Zhai, P., Stanworth, C., Liu, S., and Silberg, J.J. The human hsp70 escort protein Hep binds to the ATPase domain of mitochondrial Hsp70 and regulates nucleotide hydrolysis.  J. Biol. Chem., 283 2008: 26098-26106

Nguyen, P.Q., Liu, S., Thompson, J., and Silberg, J.J. Thermostability promotes the cooperative function of adenylate kinase fragments..  Prot. Eng. Des. Sel., 21 2008: 303-310

Drummond, D.A., Silberg, J.J., Wilke, C.O., Meyer, M.M., and Arnold, F.H. On the conservative nature of intragenic recombination.  Proc. Nat'l. Acad. Sci. U.S.A., 102 2005: 5380-5385

Bloom, J.D., Silberg, J.J., Wilke, C., Drummond, D.A., Adami, C., and Arnold, F.H. Thermodynamic prediction of protein neutrality.  Proc. Nat'l. Acad. Sci. U.S.A., 102 2005: 606-611

Cupp-Vickery, J.R., Silberg, J.J., Ta, D.T., and Vickery, L.E. Crystal structure of IscA, an iron-sulfur cluster assembly protein from Escherichia coli.  J. Mol. Biol., 338 2004: 127-137

Otey, C., Silberg, J.J., Endelman, J.B., Bandara, G., Voigt, C.A., and Arnold, F.H. Functional evolution and structural conservation in chimeric cytochromes P450: Calibrating a structure-guided approach.  Chemistry & Biology, 11 2004: 309-318

Endelman, J.B., Silberg, J.J., Wang, Z.G., and Arnold, F.H. Protein chimera library design as a shortest-path problem.  Prot. Eng. Des. & Sel., 17 2004: 589-594

Silberg, J.J., Tapley, T.L., Hoff, K.G., and Vickery, L.E. Regulation of the Hsc66 ATPase reaction cycle by the J-type cochaperone Hsc20 and the iron-sulfur escort protein IscU.  J. Biol. Chem., 279 2004: 53924-53931

Meyer, M.M., Silberg, J.J., Voigt, C.A., Endelman, J.B., Mayo, S.L., Wang, Z.G., and Arnold, F.H. Library analysis of SCHEMA-guided recombination.  Protein Science, 12 2003: 1686-1693

Hoff, K.G., Ta, D., Tapley, T.L., Silberg, J.J., and Vickery, L.E. Hsc66 substrate specificity is directed towards a discrete region of the Fe/S template protein IscU.  J. Biol. Chem., 277 2002: 27353-27359

Silberg, J.J., Hoff, K.G., Tapley, T.L., and Vickery, L.E. The Fe/S-escort protein IscU behaves as a substrate for the molecular chaperone Hsc66 from Escherichia coli.  J. Biol. Chem., 276 2002: 1696-1700

Urbina, H.D., Silberg, J.J., Hoff, K.G., and Vickery, L.E. Transfer of sulfur from IscS to IscU during iron-sulfur cluster assembly.  J. Biol. Chem., 276 2001: 44521-44526

Hoff, K.G., Silberg, J.J., and Vickery, L.E. Interaction of the iron-sulfur cluster assembly protein IscU with the Hsc66/Hsc20 molecular chaperone system in Escherichia coli.  Proc. Nat'l. Acad. Sci. U.S.A., 97 2000: 7790-7795

Silberg, J.J., and Vickery, L.E. Kinetic characterization of the ATPase cycle of the molecular chaperone Hsc66 from Escherichia coli.  J. Biol. Chem., 275 2000: 7779-7786

Silberg Research Group

  • B.S. Biology (1994) University of California Irvine
  • B.S. Chemistry (1994) University of California Irvine
  • Ph.D. Biology (2000) University of California Irvine
  • Department of Bioengineering
  • Institute of Biosciences and Bioengineering
  • Keck Center for Quantitative Biomedical Sciences
  • Systems, Synthetic, and Physical Biology
  • Chaperones, Laboratory Evolution, Mitochondrial Biochemistry, and Protein Design
Email: joff@rice.edu
Phone: 713 348-3849
Office: Keck Hall, 209