Sun Sun


Department of Chemistry & Biochemistry
The University of Texas at Austin
1 University Station A5300
Austin, TX 78712-0165





















Contact Information


Office: WEL: 5.235
Phone: 232-7811

Lab


Office:
Phone:
Fax: 471-8696

Hung-Wen (Ben) Liu


h.w.liu@mail.utexas.edu
Professor, Faculty
Professor of Pharmacy George H Hitchings Regents Chair in Drug Design

Research Group


Ben Liu Group

Education


PhD, Columbia University, 1981
BS, Tunghai University, 1974

NIEHS Postdoctoral Fellow, Massachusetts Institute of Technology 1981-84

Awards


American Chemical Society Division of Biological Chemistry, Repligen Award, 2008
Elected Academician, Academia Sinica, 2008
American Chemical Society Organic Division, Nakanishi Prize, 2007
Japan Society for the Promotion of Science Fellow, 2006
Elected Fellow, American Academy of Microbiology, 2006
Elected Fellow, American Association for the Advancement of Science, 2005
Distinguished McKnight University Professor, University of Minnesota, 1999
National Institute of General Medical Sciences MERIT Award, 1999
American Chemical Society Division of Carbohydrate Chemistry, Horace S. Isbell Award, 1993
NIH Research Career Development Award, 1990
NIEHS Postdoctoral Fellow, Massachusetts Institute of Technology, 1984

Affiliations


Institute for Cellular and Molecular Biology;

Bioorganic Chemistry and Chemical Biology


The major thrust of my research lies at the crossroads of chemistry and biology. My group is currently working on three general areas with the focus aimed at the elucidation of the mechanisms of novel enzymatic reactions and the design of methods to control and/or regulate their functions.

Enzyme Mechanism and Inhibitor Design

Using a multi-faceted approach, we study the mechanisms of enzymes involved in diverse biological processes including the formation of bacterial cell wall, biosynthesis of and resistance to antibiotics, metabolism of lipids, and the posttranslational modification of nuclear proteins. A significant effort is devoted to the synthesis of compounds as mechanistic probes or specific inhibitors for these biological catalysts.

Metabolic Pathway Engineering

Through selective disruption and/or substitution of sugar biosynthetic genes in the microorganisms which produce bioactive glycosylated secondary metabolites, we have demonstrated the feasibility of engineering nature's biosynthetic machinery for the production of novel compounds carrying designed sugar appendages. Such a combinatorial biosynthetic approach bears a great promise of finding drugs with new or improved biological activity.

Protein Function Regulation

We have recently initiated a study on poly(ADP-ribose) polymerase, an enzyme that recognizes damaged DNA and turns on the repairing machinery through polyADP-ribosylation of itself and other nuclear proteins. Such a posttranslational modification of proteins is also essential to other crucial cellular events including apoptosis. Overall, most of the biological systems under investigation are target candidates for therapeutic drugs. My group is motivated by the challenge and excitement from understanding these biological transformations and tackling the relevant biomedical problems through chemical approaches.



Representative Publications



Munos, J. W.; Pu, X.; Mansoorabadi, S. O.; Kim, H. J.; Liu, H.-w. "A Secondary Kinetic Isotope Effect Study of 1-Deoxy-D-xylulose-5-phosphate Reductoisomerase-catalyzed Reaction: Evidence for a Retroaldol-Aldol Rearrangement" J. Am. Chem. Soc. 131 (2009): 2048-2049.

Szu, P.; Ruszczucky, M.; Choi, S. H.; Yan, F.; Liu, H.-w. "Characterization and Mechanistic Studies of DesII: A Radical S-Adenosylmethionine Enzyme Involved in the Biosynthesis of TDP-D-Desosamine" J. Am. Chem. Soc. 131 (2009): in press.

Tao, Z.; Gao, P.; Hofmann, D. W.; Liu, H.-w. "Domain C of Human Poly(ADP-ribose) Polymerase-1 is Important for Enzyme Activity and Contains a Novel Zinc-Ribbon Motif." Biochemistry 47 (2008): 5804-5813.

Thibodeaux, C. J.; Melancon, C. E., III.; Liu, H.-w. "Natural Product Sugar Biosynthesis and Enzymatic Glycodiversification" Angew. Chem. Int. Ed. 47 (2008): 9814-9859.

Thibodeaux, C. J.; Melancon, C. E.; Liu, H.-w. "Unusual Sugar Biosynthesis and Natural Product Glycodiversification" Nature 446 (2007): 1008-1016.

Zhang, H.; White-Phillip, J. A.; Melancon, C. E. III; Yu, W.-l.; Kwon, H.-j.; Liu, H.-w. "Biosynthetic Studies of Kijanimicin Provide Insights into Unusual Sugar Biosynthesis and Spirotetronate Formation" J. Am. Chem. Soc. 129 (2007): 14670-14683.