The long-term goal of this research project is to understand the molecular mechanism of force production in muscle through 3-D visualization of crossbridge states stabilized with nucleotide analogues or trapped during contraction by rapid freezing. The research focuses on the structure of the large waterbug Lethocerus sp. because its filament lattice is the best ordered of all known muscles thereby making it an excellent candidate for 3-D imaging as well as facilitating the trapping of many crossbridges into similar structures. Structures observed by 3-D electron microscopy of sectioned muscle will be correlated with X-ray diffraction of native muscle and mechanical measurements on the stabilized muscle or mechanical traces made prior to freezing. Our reconstruction work will continue to focus on thin 12-30 nm sections because these specimens yield the highest detail on crossbridge structure. Oblique section reconstruction will continue to be used to produce averaged images whose transforms are readily comparable with X-ray diffraction of the native muscle. Images of crossbridges in states with a relatively high variation in structure will be studied using plus/minus 70 degrees tilt series reconstructions that do not average crossbridges. We will then explore methods for aligning, classifying and averaging 3-D crossbridge structures. Finally, we will correlate variations in crossbridge structure observed in different states with the recent atomic models of actin and the myosin motor domain. These efforts will being with modelling the known structures of myosin and actin into 3-D reconstructions of rigor and muscle treated with the non-hydrolyzable analog AMPPNP.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM030598-12
Application #
2175845
Study Section
Biophysical Chemistry Study Section (BBCB)
Project Start
1982-05-01
Project End
1995-10-31
Budget Start
1995-05-01
Budget End
1995-10-31
Support Year
12
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Duke University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Hu, Guiqing; Taylor, Dianne W; Liu, Jun et al. (2018) Identification of interfaces involved in weak interactions with application to F-actin-aldolase rafts. J Struct Biol 201:199-209
Hu, Zhongjun; Taylor, Dianne W; Edwards, Robert J et al. (2017) Coupling between myosin head conformation and the thick filament backbone structure. J Struct Biol 200:334-342
Rusu, Mara; Hu, Zhongjun; Taylor, Kenneth A et al. (2017) Structure of isolated Z-disks from honeybee flight muscle. J Muscle Res Cell Motil 38:241-250
Banerjee, Chaity; Hu, Zhongjun; Huang, Zhong et al. (2017) The structure of the actin-smooth muscle myosin motor domain complex in the rigor state. J Struct Biol 200:325-333
Hu, Zhongjun; Taylor, Dianne W; Reedy, Michael K et al. (2016) Structure of myosin filaments from relaxed Lethocerus flight muscle by cryo-EM at 6 Å resolution. Sci Adv 2:e1600058
Arakelian, Claudia; Warrington, Anthony; Winkler, Hanspeter et al. (2015) Myosin S2 origins track evolution of strong binding on actin by azimuthal rolling of motor domain. Biophys J 108:1495-1502
Winkler, Hanspeter; Taylor, Kenneth A (2013) Marker-free dual-axis tilt series alignment. J Struct Biol 182:117-24
Winkler, Hanspeter; Wu, Shenping; Taylor, Kenneth A (2013) Electron tomography of paracrystalline 2D arrays. Methods Mol Biol 955:427-60
Wu, Shenping; Liu, Jun; Reedy, Mary C et al. (2012) Structural changes in isometrically contracting insect flight muscle trapped following a mechanical perturbation. PLoS One 7:e39422
Luther, Pradeep K; Winkler, Hanspeter; Taylor, Kenneth et al. (2011) Direct visualization of myosin-binding protein C bridging myosin and actin filaments in intact muscle. Proc Natl Acad Sci U S A 108:11423-8

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