X-ray crystallographic techniques are being used to study the structures of some carcinogenic polycyclic aromatic hydrocarbons and their activated metabolites, the structures of some polycylic mutagens, and covalent products of the metabolites with nucleic acid bases, low molecular weight polynucleotides and peptides.
The aim i s to obtain information relevant to the interaction of an activated carcinogenic polycyclic aromatic hydrocarbon with its target that is critical to carcinogenesis. The mechanisms of action of carcinogen-metabolizing enzymes will be investigated by structural studies of substrates, inhibitors, and models of the active sites. We will also attempt to extract and purify some of these enzymes. We will determine the high resolution structure of the enzmye, xylose isomerase, together with the amino acid sequence of this protein. A low resolution electron density map has already been computed. In addition, attempts will be made to purify and crystallize the enzyme aconitase from mammalian and bacterial sources with the aim of obtaining the full three-dimensional structure. Mechanisms of enzyme-catalyzed reactions will be investigated by X-ray structural studies of the analogues of coenzymes B12 and biotin. Also, structures of substrates and inhibitors of enzymes, such as citrate enzymes, will be determined.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA010925-36
Application #
3163397
Study Section
Biophysics and Biophysical Chemistry B Study Section (BBCB)
Project Start
1976-04-01
Project End
1987-03-30
Budget Start
1985-04-01
Budget End
1987-03-30
Support Year
36
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Institute for Cancer Research
Department
Type
DUNS #
City
Philadelphia
State
PA
Country
United States
Zip Code
19111
Glusker, Jenny P; Carrell, H L; Kovalevsky, Andrey Y et al. (2010) Using neutron protein crystallography to understand enzyme mechanisms. Acta Crystallogr D Biol Crystallogr 66:1257-61
Kovalevsky, Andrey Y; Hanson, Leif; Fisher, S Zoe et al. (2010) Metal ion roles and the movement of hydrogen during reaction catalyzed by D-xylose isomerase: a joint x-ray and neutron diffraction study. Structure 18:688-99
Kovalevsky, Andrey Y; Katz, Amy K; Carrell, H L et al. (2008) Hydrogen location in stages of an enzyme-catalyzed reaction: time-of-flight neutron structure of D-xylose isomerase with bound D-xylulose. Biochemistry 47:7595-7
Bae, Suyeal; Mah, Heduck; Chaturvedi, Surendrakumar et al. (2007) Synthetic, crystallographic, computational, and biological studies of 1,4-difluorobenzo[c]phenanthrene and its metabolites. J Org Chem 72:7625-33