The specific aims of our proposed research program continue to focus on the problems and mechanisms of molecular recognition. Through the broad long term objectives of this research application we seek to understand the molecular mechanisms of metalloenzyme function, with specific focus on the mechanisms by which biological macromolecules recognize other macromolecular and small organic structures. Primary goals are to understand the detailed process for: (1) the recognition of a small substrate/inhibitors by a protein, (2) the structure and dynamics of specific protein - protein complexes involved in metalloprotein catalysis and (3) the mechanisms for specificity in recognition of nucleic acids by proteins. A corollary aim of our research is to develop and apply new and novel physical and chemical techniques to solve the questions of molecular recognition.
Our aim i s for these technological advances to have broad applicability to a wide variety of systems and be incorporated into the repertoire of other scientists. The question of molecular recognition is a central paradigm of molecular biology, playing central roles in most, if not all, cellular processes. Failed recognition events have been implicated in numerous disease states ranging from flawed control of gene regulation and cellular proliferation, to defects in specific metabolic activities. Our use of recombinant DNA technology, in concert with advanced biophysical methods, has proven to be ideal for understanding the fundamental mechanisms of recognition in metalloenzyme systems. Our proposed research thrust in biological oxidations utilizes as exemplary systems the cytochromes P450 which play central significance in the biotransformations of human hepatic and adrenal tissue and in the plethora of oxidative metabolism that exist across the eukaryotic, procaryotic and archaea divisions of life. Thus, the central problems of metalloenzyme biology, chemistry, and biophysics will be attacked through the selective choice of the tractable systems proposed in this application, and the combined use of recombinant DNA technology and state of the art structure-function characterization in order to place molecular mechanisms on a firm foundation for scientific understanding.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM033775-15
Application #
2743754
Study Section
Physical Biochemistry Study Section (PB)
Project Start
1984-12-01
Project End
2002-11-30
Budget Start
1998-12-01
Budget End
1999-11-30
Support Year
15
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
Mak, Piotr J; Duggal, Ruchia; Denisov, Ilia G et al. (2018) Human Cytochrome CYP17A1: The Structural Basis for Compromised Lyase Activity with 17-Hydroxyprogesterone. J Am Chem Soc 140:7324-7331
Denisov, Ilia G; Sligar, Stephen G (2017) Nanodiscs in Membrane Biochemistry and Biophysics. Chem Rev 117:4669-4713
Ye, Xin; McLean, Mark A; Sligar, Stephen G (2016) Phosphatidylinositol 4,5-Bisphosphate Modulates the Affinity of Talin-1 for Phospholipid Bilayers and Activates Its Autoinhibited Form. Biochemistry 55:5038-48
Denisov, Ilia G; Mak, Piotr J; Grinkova, Yelena V et al. (2016) The use of isomeric testosterone dimers to explore allosteric effects in substrate binding to cytochrome P450 CYP3A4. J Inorg Biochem 158:77-85
Reichart, Timothy M; Baksh, Michael M; Rhee, Jin-Kyu et al. (2016) Trimerization of the HIV Transmembrane Domain in Lipid Bilayers Modulates Broadly Neutralizing Antibody Binding. Angew Chem Int Ed Engl 55:2688-92
Carney, Christiane E; Lenov, Ivan L; Baker, Catherine J et al. (2015) Nanodiscs as a Modular Platform for Multimodal MR-Optical Imaging. Bioconjug Chem 26:899-905
Skar-Gislinge, Nicholas; Kynde, Søren A R; Denisov, Ilia G et al. (2015) Small-angle scattering determination of the shape and localization of human cytochrome P450 embedded in a phospholipid nanodisc environment. Acta Crystallogr D Biol Crystallogr 71:2412-21
Denisov, Ilia G; Grinkova, Yelena V; Baylon, Javier L et al. (2015) Mechanism of drug-drug interactions mediated by human cytochrome P450 CYP3A4 monomer. Biochemistry 54:2227-39
Mak, Piotr J; Gregory, Michael C; Denisov, Ilia G et al. (2015) Unveiling the crucial intermediates in androgen production. Proc Natl Acad Sci U S A 112:15856-61
Wilcox, Kyle C; Marunde, Matthew R; Das, Aditi et al. (2015) Nanoscale Synaptic Membrane Mimetic Allows Unbiased High Throughput Screen That Targets Binding Sites for Alzheimer's-Associated A? Oligomers. PLoS One 10:e0125263

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