This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. This proposal concerns the study of: i) the DNA repair protein, O6-alkylguanine-DNA alkyltransferase (AGT) and AlkB, from both E. coli and human; ii) a drug-resistant regulator MgrA in Staphylococcus aureus. AGT and AlkB repair the alkylation DNA base damage via direct removal of the damage. The repair activity of AGT is an important component for cellular resistance to the toxic and mutagenic effects of alkylation damage since the deleterious modification that is corrected by this family of proteins, O6-alkylguanine, represents one of the most mutagenic lesions known. We have recently solved the crystal structure of the human AGT/DNA complex with hAGT recognizing a base damage mimic. We plan to apply a chemical-crosslinking technique to stabilize AGT on normal DNA without damage. We hope to capture the structure of the non-specific DNA damage-searching mode of the repair protein. We are also working on structural studies of a very important group of DNA repair proteins, AlkB. The function of these proteins has only identified recently and this is an emerging frontier in cancer research. We are working on crystal structures of both E. coli and human AlkB proteins. Crystals of the human protein have been obtained in our group. We also work on structural studies of MgrA, a global regulator and major virulence determinant in S. aureus. Staphylococcus aureus is an important human pathogen responsible for most wound and hospital acquired infections. We demonstrate here that MgrA is a major virulence determinant during infection and is a regulator of antibiotic resistance in S. aureus. We have solved the first crystal structure of apo-MgrA at 2.8 resolution, which provides a template for designing potential therapeutic interventions for staphylococcal infections. We have obtained crystals of MgrA/DNA complexes and are also working on drug-bound MgrA structures. These works will provide insight into the regulatory mechanism of this very important protein.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR007707-15
Application #
7366198
Study Section
Special Emphasis Panel (ZRG1-BBCB (01))
Project Start
2006-08-01
Project End
2007-07-31
Budget Start
2006-08-01
Budget End
2007-07-31
Support Year
15
Fiscal Year
2006
Total Cost
$7,213
Indirect Cost
Name
University of Chicago
Department
Biochemistry
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Weingarten, Adam S; Dannenhoffer, Adam J; Kazantsev, Roman V et al. (2018) Chromophore Dipole Directs Morphology and Photocatalytic Hydrogen Generation. J Am Chem Soc 140:4965-4968
Yang, Cheolhee; Choi, Minseo; Kim, Jong Goo et al. (2018) Protein Structural Dynamics of Wild-Type and Mutant Homodimeric Hemoglobin Studied by Time-Resolved X-Ray Solution Scattering. Int J Mol Sci 19:
Kazantsev, Roman V; Dannenhoffer, Adam J; Weingarten, Adam S et al. (2017) Crystal-Phase Transitions and Photocatalysis in Supramolecular Scaffolds. J Am Chem Soc 139:6120-6127
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Cho, Hyun Sun; Schotte, Friedrich; Dashdorj, Naranbaatar et al. (2016) Picosecond Photobiology: Watching a Signaling Protein Function in Real Time via Time-Resolved Small- and Wide-Angle X-ray Scattering. J Am Chem Soc 138:8815-23
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Weingarten, Adam S; Kazantsev, Roman V; Palmer, Liam C et al. (2015) Supramolecular Packing Controls H? Photocatalysis in Chromophore Amphiphile Hydrogels. J Am Chem Soc 137:15241-6
Pfoh, Roland; Pai, Emil F; Saridakis, Vivian (2015) Nicotinamide mononucleotide adenylyltransferase displays alternate binding modes for nicotinamide nucleotides. Acta Crystallogr D Biol Crystallogr 71:2032-9
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Yang, Xiaojing; Stojkovi?, Emina A; Ozarowski, Wesley B et al. (2015) Light Signaling Mechanism of Two Tandem Bacteriophytochromes. Structure 23:1179-89

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