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Integr Biol (Camb). 2015 Oct;7(10):1285-96. doi: 10.1039/c5ib00133a. Epub 2015 Jul 9.

Mechanisms of integrin and filamin binding and their interplay with talin during early focal adhesion formation.

Author information

1
Molecular Cell Biomechanics Laboratory, Departments of Bioengineering and Mechanical Engineering, University of California Berkeley, 208A Stanley Hall #1762, Berkeley, CA 94704-1762, USA. mofrad@berkeley.edu.

Abstract

Filamin plays a key role in cellular biomechanics as an actin cross-linker and as a versatile focal adhesion binding partner. It binds directly to integrins, a family of mechanosensitive transmembrane receptors that mediate attachment to several extracellular ligands such as fibronectin, collagen, and laminin. Filamin binds β-integrin at its cytoplasmic tail, competing with talin, a major integrin activator that plays a chief role in cell adhesion. Herein, we develop molecular dynamics models to study the mechanism of early binding of αIIbβ3 integrin with filamin A (FLNa). Our models predict three important electrostatic interactions and one stabilizing hydrophobic interaction that mediate binding between filamin and integrin. In its native conformation, filamin's integrin binding site is auto-inhibited. Our models help shed light on the role of integrin binding on regulating filamin activation. Finally, the effect of talin on the filamin-integrin interaction is explored and possible scenarios of the interplay among these molecules are examined.

PMID:
26156744
DOI:
10.1039/c5ib00133a
[Indexed for MEDLINE]

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