The theme of this Program Project is to understand how molecular motor work, and in particular to elucidate the structural transitions that occur in myosin during the contractile cycle. To address these elucidate the structural transitions that occur in myosin during the contractile cycle. To address these questions, the four projects bring together a wide array of state-of-the art techniques, including single molecular mechanical measurements, in vitro motility assays, fluorescence spectroscopy, protein expression in eukaryotic systems, and protein biochemistry and characterization. In Project #1, Dr. Berger will use a spectroscopic approach, both in solution and at the single molecule level, to determine how the lever arm tilts during the contractile cycle, and at the single molecule level, to determine how the lever arm tilts during the contractile cycle, and if the cleft opens and closes to mediate its affinity for actin. Dr. Warsaw (Project #2) will use the laser trap coupled with total internal reflectance microscopy to simultaneously measure the mechanics of single myosin molecules and either the nucleotide at its active site (single molecule fluorescence), or the orientation of the lever arm (fluorescence polarization). Project #3 (Dr. Trybus) will use a mutational approach coupled to biochemical and structural techniques (cryoelectron microscopy, crystallography) to decipher how the two heads of myosin cooperate in force and motion production, how the actomyosin interface changes during the powerstroke, and if ATP hydrolysis is required for priming of the lever arm. Dr. Lowey (Project #4) proposes to test the generality of domain movements at the actomyosin interface and in the lever arm, using cryoelectron microscopic techniques. It will also be determined if the orientation of actin and myosin affect the working stroke at the single molecule level. The long-term goal is to understand how each of the structural domains of myosin contributes to chemomechanical coupling, so that it becomes possible to derive a set of design principles for molecular motors.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Program Projects (P01)
Project #
5P01AR047906-04
Application #
6758040
Study Section
Special Emphasis Panel (ZAR1-TAS-C (M2))
Program Officer
Nuckolls, Glen H
Project Start
2001-09-21
Project End
2006-05-31
Budget Start
2004-06-01
Budget End
2005-05-31
Support Year
4
Fiscal Year
2004
Total Cost
$1,296,493
Indirect Cost
Name
University of Vermont & St Agric College
Department
Physiology
Type
Schools of Medicine
DUNS #
066811191
City
Burlington
State
VT
Country
United States
Zip Code
05405
Lowey, Susan; Saraswat, Lakshmi D; Liu, HongJun et al. (2007) Evidence for an interaction between the SH3 domain and the N-terminal extension of the essential light chain in class II myosins. J Mol Biol 371:902-13
Volkmann, Niels; Lui, Hongjun; Hazelwood, Larnele et al. (2007) The R403Q myosin mutation implicated in familial hypertrophic cardiomyopathy causes disorder at the actomyosin interface. PLoS One 2:e1123
Kad, Neil M; Patlak, Joseph B; Fagnant, Patricia M et al. (2007) Mutation of a conserved glycine in the SH1-SH2 helix affects the load-dependent kinetics of myosin. Biophys J 92:1623-31
Ali, M Yusuf; Krementsova, Elena B; Kennedy, Guy G et al. (2007) Myosin Va maneuvers through actin intersections and diffuses along microtubules. Proc Natl Acad Sci U S A 104:4332-6
Rovner, Arthur S; Fagnant, Patricia M; Trybus, Kathleen M (2006) Phosphorylation of a single head of smooth muscle myosin activates the whole molecule. Biochemistry 45:5280-9
Krementsova, Elena B; Hodges, Alex R; Lu, Hailong et al. (2006) Processivity of chimeric class V myosins. J Biol Chem 281:6079-86
Debold, Edward P; Patlak, Joseph B; Warshaw, David M (2005) Slip sliding away: load-dependence of velocity generated by skeletal muscle myosin molecules in the laser trap. Biophys J 89:L34-6
Volkmann, Niels; Liu, HongJun; Hazelwood, Larnele et al. (2005) The structural basis of myosin V processive movement as revealed by electron cryomicroscopy. Mol Cell 19:595-605
Warshaw, David M; Kennedy, Guy G; Work, Steven S et al. (2005) Differential labeling of myosin V heads with quantum dots allows direct visualization of hand-over-hand processivity. Biophys J 88:L30-2
Sherwood, Jennifer J; Waller, Guillermina S; Warshaw, David M et al. (2004) A point mutation in the regulatory light chain reduces the step size of skeletal muscle myosin. Proc Natl Acad Sci U S A 101:10973-8

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