Academic Journal

Force-Dependent Interactions between Talin and Full-Length Vinculin

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Force-Dependent Interactions between Talin and Full-Length Vinculin
Συγγραφείς: Wang, Yinan, Yao, Mingxi, Baker, Karen B, Gough, Rosemarie E, Le, Shimin, Goult, Benjamin T, Yan, Jie
Στοιχεία εκδότη: American Chemical Society (ACS)
Έτος έκδοσης: 2021
Συλλογή: The University of Liverpool Repository
Περιγραφή: Talin and vinculin are part of a multicomponent system involved in mechanosensing in cell-matrix adhesions. Both exist in autoinhibited forms, and activation of vinculin requires binding to mechanically activated talin, yet how forces affect talin’s interaction with vinculin has not been investigated. Here by quantifying the kinetics of force-dependent talin-vinculin interactions using single-molecule analysis, we show that mechanical exposure of a single vinculin binding site (VBS) in talin is sufficient to relieve the autoinhibition of vinculin, resulting in high-affinity binding. We provide evidence that the vinculin undergoes dynamic fluctuations between an autoinhibited closed conformation and an open conformation that is stabilized upon binding to the VBS. Furthermore, we discover an additional level of regulation in which the mechanically exposed VBS binds vinculin significantly more tightly than the isolated VBS alone. Molecular dynamics simulations reveal the basis of this new regulatory mechanism, identifying a sensitive force-dependent change in the conformation of an exposed VBS that modulates binding. Together, these results provide a comprehensive understanding of how the interplay between force and autoinhibition provides exquisite complexity within this major mechanosensing axis.
Τύπος εγγράφου: article in journal/newspaper
Περιγραφή αρχείου: application/pdf
Γλώσσα: English
ISSN: 0002-7863
Relation: https://livrepository.liverpool.ac.uk/3179293/1/2021_Wang_JACS.pdf; Wang, Yinan, Yao, Mingxi, Baker, Karen B, Gough, Rosemarie E, Le, Shimin, Goult, Benjamin T orcid:0000-0002-3438-2807 and Yan, Jie (2021) Force-Dependent Interactions between Talin and Full-Length Vinculin JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 143 (36). pp. 14726-14737. ISSN 0002-7863, 1520-5126
DOI: 10.1021/jacs.1c06223
Διαθεσιμότητα: https://livrepository.liverpool.ac.uk/3179293/
https://doi.org/10.1021/jacs.1c06223
https://livrepository.liverpool.ac.uk/3179293/1/2021_Wang_JACS.pdf
Αριθμός Καταχώρησης: edsbas.1283CED9
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  Data: Talin and vinculin are part of a multicomponent system involved in mechanosensing in cell-matrix adhesions. Both exist in autoinhibited forms, and activation of vinculin requires binding to mechanically activated talin, yet how forces affect talin’s interaction with vinculin has not been investigated. Here by quantifying the kinetics of force-dependent talin-vinculin interactions using single-molecule analysis, we show that mechanical exposure of a single vinculin binding site (VBS) in talin is sufficient to relieve the autoinhibition of vinculin, resulting in high-affinity binding. We provide evidence that the vinculin undergoes dynamic fluctuations between an autoinhibited closed conformation and an open conformation that is stabilized upon binding to the VBS. Furthermore, we discover an additional level of regulation in which the mechanically exposed VBS binds vinculin significantly more tightly than the isolated VBS alone. Molecular dynamics simulations reveal the basis of this new regulatory mechanism, identifying a sensitive force-dependent change in the conformation of an exposed VBS that modulates binding. Together, these results provide a comprehensive understanding of how the interplay between force and autoinhibition provides exquisite complexity within this major mechanosensing axis.
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  Data: https://livrepository.liverpool.ac.uk/3179293/1/2021_Wang_JACS.pdf; Wang, Yinan, Yao, Mingxi, Baker, Karen B, Gough, Rosemarie E, Le, Shimin, Goult, Benjamin T orcid:0000-0002-3438-2807 and Yan, Jie (2021) Force-Dependent Interactions between Talin and Full-Length Vinculin JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 143 (36). pp. 14726-14737. ISSN 0002-7863, 1520-5126
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