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He is from Germany and relocated to the US
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'''Alexander Hoffmann''' is an [[United States|American]] biologist. He is the director of the [[Institute for Quantitative and Computational Biosciences]] (QCBio) and the Thomas M Asher Professor of Microbiology in the Department of Microbiology, Immunology, and Molecular Genetics (MIMG) at the [[University of California, Los Angeles]] (UCLA). His research interest is the development of a predictive understanding of how cellular and molecular networks regulate immune responses.<ref>http://signalingsystems.ucla.edu</ref>
'''Alexander Hoffmann''' is a [[German]]-[[United States|American]] biologist. He is the director of the [[Institute for Quantitative and Computational Biosciences]] (QCBio) and the Thomas M Asher Professor of Microbiology in the Department of Microbiology, Immunology, and Molecular Genetics (MIMG) at the [[University of California, Los Angeles]] (UCLA). His research interest is the development of a predictive understanding of how cellular and molecular networks regulate immune responses.<ref>http://signalingsystems.ucla.edu</ref>


== Education ==
== Education ==

Revision as of 20:12, 2 January 2022

For the German politician, see Alexander Hoffmann (politician).
Alexander Hoffmann
Alma materRockefeller University, Cambridge University
Scientific career
InstitutionsUniversity of California, Los Angeles
Doctoral advisorRobert G. Roeder
Other academic advisorsDavid Baltimore

Alexander Hoffmann is a German-American biologist. He is the director of the Institute for Quantitative and Computational Biosciences (QCBio) and the Thomas M Asher Professor of Microbiology in the Department of Microbiology, Immunology, and Molecular Genetics (MIMG) at the University of California, Los Angeles (UCLA). His research interest is the development of a predictive understanding of how cellular and molecular networks regulate immune responses.[1]

Education

Hoffmann gained his BA in Physics and Zoology at Cambridge University in 1988, pursuing research projects under the tutelage of John Gurdon and John Lasky. He obtained his Ph.D. in Biochemistry and Molecular Biology from the Rockefeller University in 1994 under the supervision of Robert G. Roeder. Working with Roeder, Hoffmann identified genes encoding the central transcription factor TFIID, including its DNA binding subunit TATA-box binding subunit.[2][3][4][5][6] He also developed the now popular His-tag expression system,[7] which facilitates the purification of recombinant proteins.[8][9]

Career

Hoffmann pursued postdoctoral research with David Baltimore at MIT from 1998, focusing on the transcriptional control of HIV, and then relocating with Baltimore to Caltech in 1998. At Caltech he focused on the transcriptional[10] and signaling functions of the immune response transcription factor NF-kB, discovering its oscillatory control.[11] Collaborating with Andre Levchenko, Hoffmann developed a mathematical model that explained the molecular basis for the complex dynamic control of NF-kB.[12] The paper describing this model is considered foundational for the field of cellular signaling.

Hoffmann established the Signaling Systems Laboratory at UCSD in 2003. A hallmark of his research is the Systems Biology research approach of iterative mathematical modeling and experimental analysis, and how kinetic and dynamic control of molecular processes confer specificity to cellular responses,.[13][14] In 2009, he co-founded the UCSD's Biocircuits Institute with Jeff Hasty and Lev Tsimring.[15] In 2010, he established the San Diego Center for Systems Biology, being awarded a "Center of Excellence" grant from the National Institutes of Health.[16] In 2013 he took a position at UCLA, and, in 2014, established the Institute for Quantitative and Computational Biosciences (QCBio).[17]

Other Roles

Hoffmann served with Pavel Pevzner as co-director of UCSD's Graduate Program in Bioinformatics from 2009-2013, overseeing a dramatic expansion and inclusion of Systems Biology, Biomedical Informatics and Quantitative Biology[18]
Hoffmann has worked to improve equity in educational opportunities. He led educational outreach programs at Caltech (Young Engineering Science Scholars,[19] Freshman Summer Institute[20]), and served at UCSD on the committee for Equity, Diversity and Inclusion, and as chair of the Chancellor's Diversity Council, focusing on student and faculty recruitment and retention practices, and institutional change.

References

  1. ^ http://signalingsystems.ucla.edu
  2. ^ Hoffmann, A., Horikoshi, M., Wang, C. K., Schroeder, S., Weil, P.A., Roeder, R.G. 1990. Cloning of the Schizosaccharomyces pombe TFIID gene reveals a strong conservation of functional domains present in Saccharomyces cerevisiae TFIID. Genes & Development 4, pp. 1141-1148
  3. ^ Hoffmann, A., Sinn, E., Yamamoto, T., Wang, J., Roy, A., Horikoshi, M., Roeder, R.G. 1990. Highly conserved core domain and unique N-terminus with presumptive regulatory motifs in a human TATA factor (TFIID). Nature 346, No.6282, pp.387-390
  4. ^ Gasch, A., Hoffmann, A., Horikoshi, M., Roeder, R.G., Chua, N.H. 1990. Arabidopsis thaliana contains two genes for TFIID. Nature 346, No.6282, pp.390-394
  5. ^ Hoffmann, A., Chiang, C.-M., Oelgeschläger, T., Burley, S.K., Nakatani, Y., Roeder, R.G. 1996 A histone octamer-like structure within TFIID. Nature 380, No.6572, pp. 356-359
  6. ^ Hoffmann, A., Oelgeschläger, T., Roeder, R.G. 1997 Considerations of transcriptional control mechanisms: Do TFIID-core promoter complexes recapitulate nucleosome-like functions ? Proc. Natl. Acad. Sci. USA 94, pp. 8928-8935
  7. ^ Hoffmann, A. and Roeder, R.G. 1991. Purification of his-tagged proteins in non-denaturing conditions suggests a convenient method for protein interaction studies. Nucleic Acids Research 19, No.22, pp. 6337-6338
  8. ^ Nikolov, D.B., Hu, S.-H., Lin, J., Gasch, A., Hoffmann, A., Horikoshi, M., Chua, N.-H., Roeder, R.G., Burley, S.K. 1992. Crystal structure of TFIID TATA-box binding protein. Nature 360, pp. 40-46
  9. ^ Xie, X.-L., Kokubo, T., Cohen, S., Mirza, U.A., Hoffmann, A., Chait, B.T., Roeder, R.G., Nakatani, Y., Burley, S.K. 1996 Structural similarity between TAFs and the heterotetrameric core of the histone octamer. Nature 380, No.6572, pp. 316-322.
  10. ^ Hoffmann, A., Leung, T.H., Baltimore, D. 2003 Genetic analysis of NF-kB/Rel transcription factors reveals molecular specificities. EMBO J., 22, pp.5530-9.
  11. ^ Hoffmann, A., Baltimore, D. 2006 Circuitry of NF-kB Signaling. Immunological Reviews, 210, pp.171-186. PMID 16623771
  12. ^ Hoffmann, A., Levchenko, A., Scott, M., Baltimore, D. 2002 The NF-B/IB signaling module: temporal control and selective gene activation. Science, 298, pp. 1241-1245
  13. ^ Behar, M., Hoffmann, A. 2010 Temporal Codes of Intra-Cellular Signals. Current Opinion in Genetics and Development, 20, pp.684-693. PMID 20956081, PMC 2982931
  14. ^ Basak, S., Behar, M., Hoffmann, A. 2012 Lessons from mathematically modeling the NFκB pathway. Immunological Reviews, 246, pp.221-38. PMID 22435558, PMC 3343698
  15. ^ http://biocircuits.ucsd.edu/
  16. ^ http://www.sdcsb.org
  17. ^ http://qcb.ucla.edu
  18. ^ http://bioinformatics.ucsd.edu
  19. ^ "Archived copy". Archived from the original on 2015-02-09. Retrieved 2018-10-10.{{cite web}}: CS1 maint: archived copy as title (link)
  20. ^ "Archived copy". Archived from the original on 2014-11-29. Retrieved 2014-10-04.{{cite web}}: CS1 maint: archived copy as title (link)
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