The best-studied molecular motors are the muscle myosins, which work in filamentous assemblies. Here we focus on unconventional myosin V, which functions as a monomer or in small numbers to transport vesicles. A comparative approach allows us to identify common principles among molecular motors, as well as to understand how variations in the kinetic cycle adapt a particular class of motors for its cellular role. The lessons learned from the regulation and function of myosin II will be applied to the design and interpretation of the experiments proposed here. The goal of specific aim #1 is to use enzymatic and in vitro motility assays to understand the molecular mechanism by which myosin V's motor activity is regulated by calcium binding to calmodulin, which binds to 6 JO motifs (consensus sequence lQxxxRGxxxR) in the neck region of myosin V. Cryoelectron microscopy will be used to assess the structural impact of calcium binding.
In specific aim #2, we will investigate the mechanism of myosin V processivity. Transient kinetics of wild type and mutant expressed myosin Vs will be used to understand the kinetic and structural features whereby the two heads of myosin V can be coordinated. Optical trapping studies (collaboration with Dr. Warshaw) will complement the biochemical studies. We will also visualize myosin V bound to actin in the presence of ATP by cryo-electron microscopy (collaboration with Drs. Hanein and Volkmann), and identify the structural elements that account for this tight binding.
Specific aim #3 is to express and isolate a small oligomer of actin for crystallization studies. We have recently been successful in developing a high-yield expression system for muscle actin. We will express mutants designed to terminate polymerization at the dimeric (or tetrameric) state for studies of the native actin-actin interface, and for potential co-crystallization efforts with myosin subfragments (collaboration with Dr. Rould). The overall goal is to exploit the unique features of other members of the myosin superfamily to more fully understand the principles by which molecular motors are designed

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL038113-19
Application #
7058730
Study Section
Special Emphasis Panel (ZRG1-SSS-B (01))
Program Officer
Lin, Michael
Project Start
1987-04-01
Project End
2008-05-31
Budget Start
2006-07-01
Budget End
2008-05-31
Support Year
19
Fiscal Year
2006
Total Cost
$369,849
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
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Lowey, Susan; Bretton, Vera; Gulick, James et al. (2013) Transgenic mouse ?- and ?-cardiac myosins containing the R403Q mutation show isoform-dependent transient kinetic differences. J Biol Chem 288:14780-7
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