A complete understanding of phenomena such as morphogenesis, wound healing, and viral transformation is contingent upon an understanding of fundamental cell processes such as motility, the maintenance and change of cell shape, and cell-cell and cell-substrate attachment. At the core of our ignorance about these basic life processes is a lack of knowledge about the molecular details of transmembrane interactions between the cytoskeleton and the cell surface. The ameboid stage of the cellular slime mold, Dictyostelium discoideum is easily grown in large quantities, is motile, and exhibits cell-cell as well as cell-substrate attachment. Using D. discoideum as a model for cells in general, I am investigating the interactions between this cell's plasma membrane and its cytoplasmic cytoskeletal proteins. In the past three years we have isolated cell-cell contact regions from aggregated amebae, and have developed two new low-speed sedimentation binding assays to monitor associations between actin and membranes. We find that integral proteins mediate a specific, saturable binding of plasma membranes to the sides of actin filaments and that plasma membranes can catalyze the polymerization of actin at the membrane surface even at actin concentrations well below the normal critical concentration for polymerization. Using detergent solubilization and F-actin affinity chromatography, we have identified an integral actin-binding protein with an apparent molecular weight of 17,000 daltons. The immediate goals are to characterize and reconstitute the 17kd protein, to use chemical crosslinking to identify detergent-sensitive actin-binding proteins missed by F-actin affinity chromatography, to prepare monospecific antibodies against the major integral membrane components of an ameboid membrane cytoskeleton, to explore the structure and regulation of the transmembrane linkages in this system, and to determine whether structurally similar linkages are found in other species. Of ultimate interest is the molecular basis for motility and cell-cell and cell-substrate interactions.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033048-07
Application #
3282377
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1988-07-01
Project End
1991-12-31
Budget Start
1989-01-01
Budget End
1989-12-31
Support Year
7
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Worcester Foundation for Biomedical Research
Department
Type
DUNS #
City
Shrewsbury
State
MA
Country
United States
Zip Code
01545
Son, Kyonghee; Smith, Tara C; Luna, Elizabeth J (2015) Supervillin binds the Rac/Rho-GEF Trio and increases Trio-mediated Rac1 activation. Cytoskeleton (Hoboken) 72:47-64
Spinazzola, Janelle M; Smith, Tara C; Liu, Min et al. (2015) Gamma-sarcoglycan is required for the response of archvillin to mechanical stimulation in skeletal muscle. Hum Mol Genet 24:2470-81
Lawlor, Michael W; Viola, Marissa G; Meng, Hui et al. (2014) Differential muscle hypertrophy is associated with satellite cell numbers and Akt pathway activation following activin type IIB receptor inhibition in Mtm1 p.R69C mice. Am J Pathol 184:1831-42
Fang, Zhiyou; Luna, Elizabeth J (2013) Supervillin-mediated suppression of p53 protein enhances cell survival. J Biol Chem 288:7918-29
Fedechkin, Stanislav O; Brockerman, Jacob; Luna, Elizabeth J et al. (2013) An N-terminal, 830 residues intrinsically disordered region of the cytoskeleton-regulatory protein supervillin contains Myosin II- and F-actin-binding sites. J Biomol Struct Dyn 31:1150-9
Smith, Tara C; Fridy, Peter C; Li, Yinyin et al. (2013) Supervillin binding to myosin II and synergism with anillin are required for cytokinesis. Mol Biol Cell 24:3603-19
Edelstein, Leonard C; Luna, Elizabeth J; Gibson, Ian B et al. (2012) Human genome-wide association and mouse knockout approaches identify platelet supervillin as an inhibitor of thrombus formation under shear stress. Circulation 125:2762-71
Bhuwania, Ridhirama; Cornfine, Susanne; Fang, Zhiyou et al. (2012) Supervillin couples myosin-dependent contractility to podosomes and enables their turnover. J Cell Sci 125:2300-14
Hao, Zhikui; Cai, Yujie; Liao, Xiangru et al. (2011) Chitinolyticbacter meiyuanensis SYBC-H1T, gen. nov., sp. nov., a chitin-degrading bacterium isolated from soil. Curr Microbiol 62:1732-8
Fang, Zhiyou; Takizawa, Norio; Wilson, Korey A et al. (2010) The membrane-associated protein, supervillin, accelerates F-actin-dependent rapid integrin recycling and cell motility. Traffic 11:782-99

Showing the most recent 10 out of 48 publications