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. 2019 Sep 11;19(9):5982-5990.
doi: 10.1021/acs.nanolett.9b01732. Epub 2019 Aug 13.

Force-Dependent Regulation of Talin-KANK1 Complex at Focal Adhesions

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Free article

Force-Dependent Regulation of Talin-KANK1 Complex at Focal Adhesions

Miao Yu et al. Nano Lett. .
Free article

Abstract

KANK proteins mediate cross-talk between dynamic microtubules and integrin-based adhesions to the extracellular matrix. KANKs interact with the integrin/actin-binding protein talin and with several components of microtubule-stabilizing cortical complexes. Because of actomyosin contractility, the talin-KANK complex is likely under mechanical force, and its mechanical stability is expected to be a critical determinant of KANK recruitment to focal adhesions. Here, we quantified the lifetime of the complex of the talin rod domain R7 and the KN domain of KANK1 under shear-force geometry and found that it can withstand forces for seconds to minutes over a physiological force range up to 10 pN. Complex stability measurements combined with cell biological experiments suggest that shear-force stretching promotes KANK1 localization to the periphery of focal adhesions. These results indicate that the talin-KANK1 complex is mechanically strong, enabling it to support the cross-talk between microtubule and actin cytoskeleton at focal adhesions.

Keywords: KANK1; focal adhesions; magnetic tweezers; mechanotransduction; talin.

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