This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.The actin cytoskeleton near the protruding cell edge consists of two kinetically, kinematically, molecularly, and materially distinct networks. Only one of the two, which we refer to as the lamellipodium, has the properties of an Arp2/3-controlled, dendritically branched and treadmilling network. The second network, referred to as the lamella, does contain Arp2/3 as well, but its polymerization is largely independent of Arp2/3 activity. We hypothesize that the assembly of F-actin in the lamella is mediated by formins and tropomyosin.
The aim of this project is to implement a Virtual Cell (VC) model of F-actin network assembly at the leading edge to predict the differential kinetics of simultaneous Arp2/3- and formin-mediated lamellipodium and lamella formation.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR013186-11
Application #
7722730
Study Section
Special Emphasis Panel (ZRG1-CB-L (40))
Project Start
2008-08-01
Project End
2009-04-30
Budget Start
2008-08-01
Budget End
2009-04-30
Support Year
11
Fiscal Year
2008
Total Cost
$27,639
Indirect Cost
Name
University of Connecticut
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
022254226
City
Farmington
State
CT
Country
United States
Zip Code
06030
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