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Research GroupBen Liu Group |
EducationBS, Tunghai University, 1974 PhD, Columbia University, 1981 NIEHS Postdoctoral Fellow, Massachusetts Institute of Technology 1981-84 |
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AwardsAmerican Chemical Society Division of Biological Chemistry, Repligen Award, 2008 American Chemical Society Organic Division, Nakanishi Prize, 2007 Elected Fellow, American Academy of Microbiology, 2006 Japan Society for the Promotion of Science Fellow, 2006 Elected Fellow, American Association for the Advancement of Science, 2005 National Institute of General Medical Sciences MERIT Award, 1999 Distinguished McKnight University Professor, University of Minnesota, 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 |
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.