The role of focal adhesion anchoring domains of CAS in mechanotransduction

• Published in: Scientific reports Vol. 7; no. 1; p. 46233
• Main Authors: Braniš, Jaroslav, Pataki, Csilla, Spörrer, Marina, Gerum, Richard C., Mainka, Astrid, Cermak, Vladimir, Goldmann, Wolfgang H., Fabry, Ben, Brabek, Jan, Rosel, Daniel
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 13.04.2017; Nature Publishing Group
• Subjects: 13/51; 13/95; 14/19; 631/57/2272; 631/80/79/2066; Adhesion; Antibodies; Binding sites; Biosensors; Cellular apoptosis susceptibility protein; Deletion mutant; Extracellular matrix; Humanities and Social Sciences; Localization; Mechanotransduction; multidisciplinary; Phosphorylation; Proteins; Science
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep46233

CAS is a docking protein, which was shown to act as a mechanosensor in focal adhesions. The unique assembly of structural domains in CAS is important for its function as a mechanosensor. The tension within focal adhesions is transmitted to a stretchable substrate domain of CAS by focal adhesion-targeting of SH3 and CCH domain of CAS, which anchor the CAS protein in focal adhesions. Mechanistic models of the stretching biosensor propose equal roles for both anchoring domains. Using deletion mutants and domain replacements, we have analyzed the relative importance of the focal adhesion anchoring domains on CAS localization and dynamics in focal adhesions as well as on CAS-mediated mechanotransduction. We confirmed the predicted prerequisite of the focal adhesion targeting for CAS-dependent mechanosensing and unraveled the critical importance of CAS SH3 domain in mechanosensing. We further show that CAS localizes to the force transduction layer of focal adhesions and that mechanical stress stabilizes CAS in focal adhesions.