Cell migration plays an integral role in many processes important for human health, including embryonic development, immunological response and metastasis. Ena/VASP proteins are key regulators of cell migration. Ena/VASP proteins bind to the barbed ends of filamentous actin and induce changes in the geometry of the actin cytoskeleton that include increased actin filament length. The overall goal of this proposal is to determine if Ena/VASP functions as an """"""""anti-capping"""""""" protein, causing alteration of the actin network by shielding the barbed ends of actin from capping protein. To test this hypothesis, levels of capping protein activity will be altered in cells to determine if reciprocal changes in actin cytoskeleton geometry can be achieved. In vitro actin polymerization experiments will be performed to directly measure antagonism between Ena/VASP and capping protein. Microscopy will be used to detect binding of Ena/VASP to barbed ends and to determine if the anti-capping mechanism involves exclusion of capping protein from the barbed ends. Finally, Ena/VASP mutants will be used to determine domains necessary for anti-capping function and to test if phosphorylation of Ena/VASP by PKA regulates anti-capping activity.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM071156-02
Application #
6888532
Study Section
Special Emphasis Panel (ZRG1-F05 (20))
Program Officer
Rodewald, Richard D
Project Start
2004-05-01
Project End
2006-04-30
Budget Start
2005-05-01
Budget End
2006-04-30
Support Year
2
Fiscal Year
2005
Total Cost
$49,928
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Dent, Erik W; Kwiatkowski, Adam V; Mebane, Leslie M et al. (2007) Filopodia are required for cortical neurite initiation. Nat Cell Biol 9:1347-59