Our goal is to determine which cellular movements require myosin for force production and to understand, on the molecular level, the mechanisms of myosin function in vitro and in vivo. Our approach has been to produce and characterize monoclonal, site-specific antibodies to cytoplasmic myosin as probes of myosin function in Acanthamoeba. We will analyze force production by myosin with purified proteins, in cell free model systems and in living cells through microinjection. Acanthamoeba contains two classes of myosin that are morphologically distinct. The role these two myosins play in cell movement is not known. In vitro, we have and will map antibody binding sites by electron microscopy of antibody-myosin complexes and by antibody binding to myosin peptides. We have and will analyze the interaction of antibodies with purified contractile proteins to determine how distinct domains in the myosin molecule contribute to myosin filament formation, actin binding and actin-activated ATPase activity. We have and will apply the antibodies to cell free model systems of contractility. To date we have characterized 23 monoclonal antibodies directed against at least 15 unique sites distributed from the myosin-II head to the tip of its tail. Two antibodies block polymerization, 12 block actomyosin-II ATPase activity and 14 inhibit contraction of gelled extracts of amoeba cytoplasm. Our data shows that regions near the tip of the myosin tail are required for polymerization and that another domain on the myosin tail, close to the myosin head, is essential for ATPase activity and force production. Finally, we have and will probe myosin function in whole cells. Fluorescent antibody staining of fixed cells, electron microscopy of antibody stained frozen thin sections, and the distribution of labeled myosin microinjected into living cells will localize myosin. Most significantly, we will microinject the antibodies into living cells to determine which motilities (locomotion, cytokinesis, etc.) require myosin function. We are encouraged by preliminary microinjection studies on Acanthamoeba, and by our antibody-microinjection studies on myosin function in starfish eggs, which showed that myosin is necessary for cytokinesis but not chromosome movement. By analyzing antibody effects on biochemical function, on contractility in vitro, on the location of myosin in whole cells, and on motility in vivo, we expect to elucidate the molecular mechanism of myosin function in living cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033830-02
Application #
3283908
Study Section
Molecular Cytology Study Section (CTY)
Project Start
1984-09-30
Project End
1987-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
2
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Harvard University
Department
Type
Schools of Arts and Sciences
DUNS #
071723621
City
Cambridge
State
MA
Country
United States
Zip Code
Mortensen, Richard D; Moore, Regan P; Fogerson, Stephanie M et al. (2018) Identifying Genetic Players in Cell Sheet Morphogenesis Using a Drosophila Deficiency Screen for Genes on Chromosome 2R Involved in Dorsal Closure. G3 (Bethesda) 8:2361-2387
Lo, Wei-Chang; Madrak, Craig; Kiehart, Daniel P et al. (2018) Unified biophysical mechanism for cell-shape oscillations and cell ingression. Phys Rev E 97:062414
Aristotelous, A C; Crawford, J M; Edwards, G S et al. (2018) Mathematical models of dorsal closure. Prog Biophys Mol Biol 137:111-131
Guo, Yuting; Li, Di; Zhang, Siwei et al. (2018) Visualizing Intracellular Organelle and Cytoskeletal Interactions at Nanoscale Resolution on Millisecond Timescales. Cell 175:1430-1442.e17
Kiehart, Daniel P; Crawford, Janice M; Aristotelous, Andreas et al. (2017) Cell Sheet Morphogenesis: Dorsal Closure in Drosophila melanogaster as a Model System. Annu Rev Cell Dev Biol 33:169-202
Cao, Jingli; Wang, Jinhu; Jackman, Christopher P et al. (2017) Tension Creates an Endoreplication Wavefront that Leads Regeneration of Epicardial Tissue. Dev Cell 42:600-615.e4
Lu, Heng; Sokolow, Adam; Kiehart, Daniel P et al. (2016) Quantifying dorsal closure in three dimensions. Mol Biol Cell 27:3948-3955
Marston, Daniel J; Higgins, Christopher D; Peters, Kimberly A et al. (2016) MRCK-1 Drives Apical Constriction in C. elegans by Linking Developmental Patterning to Force Generation. Curr Biol 26:2079-89
Goldstein, Bob; Kiehart, Daniel P (2015) Moving Inward: Establishing the Mammalian Inner Cell Mass. Dev Cell 34:385-6
Lu, Heng; Sokolow, Adam; Kiehart, Daniel P et al. (2015) Remodeling Tissue Interfaces and the Thermodynamics of Zipping during Dorsal Closure in Drosophila. Biophys J 109:2406-17

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