The primary goal of this project is to determine the solution tertiary structure of putidaredoxin (Pdx), a 11.6 kD protein consisting of a single 106-residue polypeptide chain and a 2Fe-2S prosthetic group. The determination will be performed using phase-sensitive two dimensional NMR methods, including direct and relayed coherence transfer 1H experiments, homo- and heteronuclear multiple-quantum, Hartmann-Hahn coherence transfer and NOESY experiments. Pdx has bee cloned and is readily isolated from the bacterial expression system which we employ. NMR samples will be prepared both as natural abundance samples for 1H experiments and isotopically labeled with 13C and 15N either randomly or site-specifically for inverse detection experiments. Knowledge of the solution structure of Pdx is critical for a complete understanding of the mechanism of electron transfer between Pdx and its physiological redox partners, Pdx reductase and P-450cam. However, no structure has yet been assigned by X-ray crystallographic methods because of difficulty in obtaining suitable crystals, and NMR methods offer the best route to a rapid determination of tertiary structure. Pdx acts as both reductant and effector for the ternary complex of P- 450cam, camphor and O2 which results in the 5-exo-hydroxylation of camphor in the first step in camphor catabolism by Pseudomonas. The camphor hydroxylase system has been studied for many years as a model for monooxygenase activity, which is important in myriad biological processes, including hormone biosynthesis and carcinogen activation. In the course of this project, we also will be investigating the mechanism of recognition and incorporation of the 2Fe-2S center into Pdx, determining the solution structure of the apoprotein by NMR and its relationship to the holoprotein and observing the thermodynamics of the transitions between folded and unfolded states in the apo- and holoproteins calorimetrically.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29GM044191-05
Application #
2182417
Study Section
Metallobiochemistry Study Section (BMT)
Project Start
1990-04-01
Project End
1995-03-31
Budget Start
1994-04-01
Budget End
1995-03-31
Support Year
5
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Brandeis University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
616845814
City
Waltham
State
MA
Country
United States
Zip Code
02454
Li, Shengying; Tietz, Drew R; Rutaganira, Florentine U et al. (2012) Substrate recognition by the multifunctional cytochrome P450 MycG in mycinamicin hydroxylation and epoxidation reactions. J Biol Chem 287:37880-90
Herbst, Robert W; Perovic, Iva; Martin-Diaconescu, Vlad et al. (2010) Communication between the zinc and nickel sites in dimeric HypA: metal recognition and pH sensing. J Am Chem Soc 132:10338-51
Asciutto, Eliana K; Madura, Jeffry D; Pochapsky, Susan Sondej et al. (2009) Structural and dynamic implications of an effector-induced backbone amide cis-trans isomerization in cytochrome P450cam. J Mol Biol 388:801-14