Awardee OrganizationWORCESTER FOUNDATION FOR BIOMEDICAL RES
Description
Abstract Text
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.
No Sub Projects information available for 5R01GM033048-09
Publications
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