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Mechanical activation of vinculin binding to talin locks talin in an unfolded conformation.

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posted on 2015-04-16, 13:11 authored by M. Yao, Benjamin T. Goult, H. Chen, P. Cong, M. P. Sheetz, J. Yan
The force-dependent interaction between talin and vinculin plays a crucial role in the initiation and growth of focal adhesions. Here we use magnetic tweezers to characterise the mechano-sensitive compact N-terminal region of the talin rod, and show that the three helical bundles R1-R3 in this region unfold in three distinct steps consistent with the domains unfolding independently. Mechanical stretching of talin R1-R3 enhances its binding to vinculin and vinculin binding inhibits talin refolding after force is released. Mutations that stabilize R3 identify it as the initial mechano-sensing domain in talin, unfolding at ∼5 pN, suggesting that 5 pN is the force threshold for vinculin binding and adhesion progression.

Funding

This work was supported by the National Research Foundation of Singapore through the Mechanobiology Institute at National University of Singapore (to J.Y. and M.P.S.), and NIH grant #EB001480 (to M.P.S.).

History

Citation

Scientific Reports, 2014, 4:4610

Author affiliation

/Organisation/COLLEGE OF MEDICINE, BIOLOGICAL SCIENCES AND PSYCHOLOGY/School of Biological Sciences/Department of Biochemistry

Version

  • VoR (Version of Record)

Published in

Scientific Reports

Publisher

Nature Publishing Group

issn

2045-2322

eissn

2045-2322

Available date

2015-04-16

Publisher version

http://www.nature.com/srep/2014/140409/srep04610/full/srep04610.html

Notes

PMCID: PMC3980218

Language

en

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