Ontology highlight
ABSTRACT:
SUBMITTER: Kalli AC
PROVIDER: S-EPMC3032884 | biostudies-literature | 2010 Oct
REPOSITORIES: biostudies-literature
Kalli Antreas C AC Wegener Kate L KL Goult Benjamin T BT Anthis Nicholas J NJ Campbell Iain D ID Sansom Mark S P MS
Structure (London, England : 1993) 20101001 10
Integrins are cell surface receptors crucial for cell migration and adhesion. They are activated by interactions of the talin head domain with the membrane surface and the integrin β cytoplasmic tail. Here, we use coarse-grained molecular dynamic simulations and nuclear magnetic resonance spectroscopy to elucidate the membrane-binding surfaces of the talin head (F2-F3) domain. In particular, we show that mutations in the four basic residues (K258E, K274E, R276E, and K280E) in the F2 binding surf ...[more]