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The Thermodynamics and Kinetics of Focal Adhesion Dynamics
The Thermodynamics and Kinetics of Focal Adhesion Dynamics
By Professor Krishna Garikipati
University of Michigan Mechanical Engineering and Michigan Center for Theoretical Physics
Thu, Feb 5, 2009 2:30 PM
Location: Cupples II, Room 100
The free energy that drives growth, resorption and sliding of focal adhesions includes mechanical and chemical contributions. We have identified a competition among four effects that control focal adhesion dynamics: (1) work done during addition of complexes, (2) the chemical potential inherent to focal adhesions, (3) the elastic free energy associated with deformation of focal adhesions, and (4) work done on a molecular conformational change. A theoretical treatment of focal adhesion dynamics developed in the framework of kinetic processes driven by out of equilibrium thermodynamic forces demonstrates that the mechanisms governed by these four effects allow focal adhesions to exhibit a rich variety of behavior without the need to introduce special constitutive assumptions. In this treatment, the structural unit of focal adhesions is a complex consisting of a ligand such as fibronectin, an integrin molecule, and associated plaque proteins. The binding and unbinding of these complexes causes focal adhesion growth and resorption, respectively. The reaction-limited case is considered. Our central findings are that growth, resorption and sliding are all predicted by a very simple chemo-mechanical model. Sliding requires symmetry breaking and is achieved via (1) above; (4) promotes symmetric growth, and (2) and (3) cause symmetric desorption.
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Mechanical, Aerospace & Structural Engineering, Washington University in St. Louis
One Brookings Drive, Box 1185, St. Louis, Missouri 63130
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