| Literature DB >> 29074139 |
Maximilian Hörner1, Claire Chatelle2, Wignand W D Mühlhäuser3, David R Stocker4, Michael Coats5, Wilfried Weber6, Gerald Radziwill7.
Abstract
Focal adhesion kinase (FAK) integrates signaling from integrins, growth factor receptors and mechanical stress to control cell adhesion, motility, survival and proliferation. Here, we developed a single-component, photo-activatable FAK, termed optoFAK, by using blue light-induced oligomerization of cryptochrome 2 (CRY2) to activate FAK-CRY2 fusion proteins. OptoFAK functions uncoupled from physiological stimuli and activates downstream signaling rapidly and reversibly upon blue light exposure. OptoFAK stimulates SRC creating a positive feedback loop on FAK activation, facilitating phosphorylation of paxillin and p130Cas in adherent cells. In detached cells or in mechanically stressed adherent cells, optoFAK is autophosphorylated upon exposure to blue light, however, downstream signaling is hampered indicating that the accessibility to these substrates is disturbed. OptoFAK may prove to be a useful tool to study the biological function of FAK in growth factor and integrin signaling, tension-mediated focal adhesion maturation or anoikis and could additionally serve as test system for kinase inhibitors.Entities:
Keywords: Cryptochrome 2; Feedback loop; Focal adhesion kinase; Kinase inhibitor; Optogenetics; Signaling
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Year: 2017 PMID: 29074139 DOI: 10.1016/j.cellsig.2017.10.012
Source DB: PubMed Journal: Cell Signal ISSN: 0898-6568 Impact factor: 4.315