We will extend our studies of the mechanism by which chemical energy is transformed into mechanical energy by motors from the myosin and kinesin families. The approach for the kinesin motors will build on our previous work which determined the structures of several of the microtubule based motors in multiple conformations, and which used spectroscopic methods to determine how these structures changed during the cycle. We will obtain structures for new members of the kinesin family. We will investigate the conformational changes that occur in these structures by obtaining dynamic information using spectroscopic probes, both fluorescent and paramagnetic. We will expand our knowledge of the neckdocking mechanism of conventional kinesin. We will initiate studies of NCD, which may work through a mechanism very different from kinesin. Myosin VI is a processive motor with a long step, but a short lever arm, and spectroscopic probes will be used to investigate this unusual motor. In addition we will investigate the structure and function of both the motor region and the cargo-binding region of a member of another motor family, dynein. These structural and functional data will be complemented by measurements of motor mechanics. Oligomers of the actin filament and their complexes with myosin fragments will be formed, and their properties and structures determined. We will initiate a new direction for our program, and investigate the cargo domains of the motor proteins and identify their protein partners that together connect the motors to their loads. The cargo domains are less well characterized than are the motor domains, and only a few of their many partners are known. We will employ chemical, structural, biochemical, and genetic techniques to identify the proteins involved in cargo recognition, determine structures for selected cargo binding domains and their partners, and characterize their function. In summary, our goal of understanding the mechanism of biological motors requires: a) determination of their atomic resolution structures, b) knowledge of how these structures change in specific states, and c) measurements of the mechanics and energetics associated with these states. In this program we have brought together a unique group of investigators that can extend our knowledge in each of these areas leading to a better picture of the molecular mechanism of these two motors that produce force and motion.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Research Program Projects (P01)
Project #
5P01AR042895-13
Application #
7115745
Study Section
Special Emphasis Panel (ZAR1-TEN-A (M1))
Program Officer
Nuckolls, Glen H
Project Start
1997-07-01
Project End
2009-06-30
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
13
Fiscal Year
2006
Total Cost
$1,022,110
Indirect Cost
Name
University of California San Francisco
Department
Biochemistry
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Lal, Sean; Li, Amy; Allen, David et al. (2015) Best Practice BioBanking of Human Heart Tissue. Biophys Rev 7:399-406
Eldred, Catherine C; Naber, Nariman; Pate, Edward et al. (2013) Conformational changes at the nucleotide site in the presence of bound ADP do not set the velocity of fast Drosophila myosins. J Muscle Res Cell Motil 34:35-42
Harrington, Timothy D; Naber, Nariman; Larson, Adam G et al. (2011) Analysis of the interaction of the Eg5 Loop5 with the nucleotide site. J Theor Biol 289:107-15
Purcell, Thomas J; Naber, Nariman; Franks-Skiba, Kathy et al. (2011) Nucleotide pocket thermodynamics measured by EPR reveal how energy partitioning relates myosin speed to efficiency. J Mol Biol 407:79-91
Waitzman, Joshua S; Larson, Adam G; Cochran, Jared C et al. (2011) The loop 5 element structurally and kinetically coordinates dimers of the human kinesin-5, Eg5. Biophys J 101:2760-9
Purcell, Thomas J; Naber, Nariman; Sutton, Shirley et al. (2011) EPR spectra and molecular dynamics agree that the nucleotide pocket of myosin V is closed and that it opens on binding actin. J Mol Biol 411:16-26
Naber, Nariman; Larson, Adam; Rice, Sarah et al. (2011) Multiple conformations of the nucleotide site of Kinesin family motors in the triphosphate state. J Mol Biol 408:628-42
Naber, Nariman; Málnási-Csizmadia, András; Purcell, Thomas J et al. (2010) Combining EPR with fluorescence spectroscopy to monitor conformational changes at the myosin nucleotide pocket. J Mol Biol 396:937-48
Larson, Adam G; Naber, Nariman; Cooke, Roger et al. (2010) The conserved L5 loop establishes the pre-powerstroke conformation of the Kinesin-5 motor, eg5. Biophys J 98:2619-27
Stewart, Melanie A; Franks-Skiba, Kathleen; Chen, Susan et al. (2010) Myosin ATP turnover rate is a mechanism involved in thermogenesis in resting skeletal muscle fibers. Proc Natl Acad Sci U S A 107:430-5

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