The long term goal of this project is to understand how the catalytic reaction of the hydrolysis or synthesis of adenosine triphosphate is coupled to the transport of protons across the membrane in the multi-subunit FOF 1 ATP synthase. Recent observations have established that the catalytic and transport functions utilize rotational mechanisms and energy is transferred between them, in part, by the torque generated on the rotor subunits. Characterization of several mutant enzymes with substitutions in the interfaces between rotor and stator indicate that the efficiency of energy transfer between transport and catalysis involves transmission of conformational information. To understand how the conformational effects modulate the catalytic and transport mechanisms, we will carry out two Specific Aims.
Specific Aim 1 : the site-directed spin labeling strategy of EPR spectroscopy and determination of solvent accessibility of cysteine substitutions by reactivity with hydrophilic sulfhydryl reagents will be used to generate a structure-function map of the gamma and epsilon rotor subunits. Physical properties of the rotor and how it interacts with the stator will be elucidated.
Specific Aim 2 : we will dissect the coordination between the catalytic transition state and the rotational behavior of the catalytic motor. The effects of amino acid replacements on ATP-driven gamma subunit rotation, which is observed directly on a nano-fabricated experimental platform, will be correlated to the partial reaction steps of the catalytic mechanism, which are determined chemically by pre-steady state quench-flow and fluorescence stopped-flow kinetic measurements. Mutant enzymes will be analyzed that have amino acid replacements that perturb rotor-stator interactions and have effects on the catalytic transition state and rotation. These studies seek to understand the molecular mechanisms of a true molecular rotary motor, and in particular, the mechanisms of coupling efficiency that generate high torque forces which makes it the most powerful nanoelectromechanical motor.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM050957-11
Application #
6741964
Study Section
Special Emphasis Panel (ZRG1-SSS-B (01))
Program Officer
Preusch, Peter C
Project Start
1994-05-01
Project End
2006-04-30
Budget Start
2004-05-01
Budget End
2005-04-30
Support Year
11
Fiscal Year
2004
Total Cost
$294,217
Indirect Cost
Name
University of Virginia
Department
Physiology
Type
Schools of Medicine
DUNS #
065391526
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Sekiya, Mizuki; Hosokawa, Hiroyuki; Nakanishi-Matsui, Mayumi et al. (2010) Single molecule behavior of inhibited and active states of Escherichia coli ATP synthase F1 rotation. J Biol Chem 285:42058-67
Sekiya, Mizuki; Nakamoto, Robert K; Al-Shawi, Marwan K et al. (2009) Temperature dependence of single molecule rotation of the Escherichia coli ATP synthase F1 sector reveals the importance of gamma-beta subunit interactions in the catalytic dwell. J Biol Chem 284:22401-10
Nakamoto, Robert K; Baylis Scanlon, Joanne A; Al-Shawi, Marwan K (2008) The rotary mechanism of the ATP synthase. Arch Biochem Biophys 476:43-50
Scanlon, Joanne A Baylis; Al-Shawi, Marwan K; Nakamoto, Robert K (2008) A rotor-stator cross-link in the F1-ATPase blocks the rate-limiting step of rotational catalysis. J Biol Chem 283:26228-40
Scanlon, Joanne A Baylis; Al-Shawi, Marwan K; Le, Nga Phi et al. (2007) Determination of the partial reactions of rotational catalysis in F1-ATPase. Biochemistry 46:8785-97
Mnatsakanyan, Nelli; Bagramyan, Karine; Vassilian, Anait et al. (2002) F0 cysteine, bCys21, in the Escherichia coli ATP synthase is involved in regulation of potassium uptake and molecular hydrogen production in anaerobic conditions. Biosci Rep 22:421-30
Andrews, S H; Peskova, Y B; Polar, M K et al. (2001) Conformation of the gamma subunit at the gamma-epsilon-c interface in the complete Escherichia coli F(1)-ATPase complex by site-directed spin labeling. Biochemistry 40:10664-70
Nakamoto, R K; Ketchum, C J; Kuo, P H et al. (2000) Molecular mechanisms of rotational catalysis in the F(0)F(1) ATP synthase. Biochim Biophys Acta 1458:289-99
Le, N P; Omote, H; Wada, Y et al. (2000) Escherichia coli ATP synthase alpha subunit Arg-376: the catalytic site arginine does not participate in the hydrolysis/synthesis reaction but is required for promotion to the steady state. Biochemistry 39:2778-83
Peskova, Y B; Nakamoto, R K (2000) Catalytic control and coupling efficiency of the Escherichia coli FoF1 ATP synthase: influence of the Fo sector and epsilon subunit on the catalytic transition state. Biochemistry 39:11830-6

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