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Activation of von Willebrand factor via mechanical unfolding of its discontinuous autoinhibitory module

Von Willebrand factor (VWF) activates in response to shear flow to initiate hemostasis, while aberrant activation could lead to thrombosis. Above a critical shear force, the A1 domain of VWF becomes activated and captures platelets via the GPIb-IX complex. Here we show that the shear-responsive elem...

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Autores principales: Arce, Nicholas A., Cao, Wenpeng, Brown, Alexander K., Legan, Emily R., Wilson, Moriah S., Xu, Emma-Ruoqi, Berndt, Michael C., Emsley, Jonas, Zhang, X. Frank, Li, Renhao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060278/
https://www.ncbi.nlm.nih.gov/pubmed/33883551
http://dx.doi.org/10.1038/s41467-021-22634-x
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author Arce, Nicholas A.
Cao, Wenpeng
Brown, Alexander K.
Legan, Emily R.
Wilson, Moriah S.
Xu, Emma-Ruoqi
Berndt, Michael C.
Emsley, Jonas
Zhang, X. Frank
Li, Renhao
author_facet Arce, Nicholas A.
Cao, Wenpeng
Brown, Alexander K.
Legan, Emily R.
Wilson, Moriah S.
Xu, Emma-Ruoqi
Berndt, Michael C.
Emsley, Jonas
Zhang, X. Frank
Li, Renhao
author_sort Arce, Nicholas A.
collection PubMed
description Von Willebrand factor (VWF) activates in response to shear flow to initiate hemostasis, while aberrant activation could lead to thrombosis. Above a critical shear force, the A1 domain of VWF becomes activated and captures platelets via the GPIb-IX complex. Here we show that the shear-responsive element controlling VWF activation resides in the discontinuous autoinhibitory module (AIM) flanking A1. Application of tensile force in a single-molecule setting induces cooperative unfolding of the AIM to expose A1. The AIM-unfolding force is lowered by truncating either N- or C-terminal AIM region, type 2B VWD mutations, or binding of a ristocetin-mimicking monoclonal antibody, all of which could activate A1. Furthermore, the AIM is mechanically stabilized by the nanobody that comprises caplacizumab, the only FDA-approved anti-thrombotic drug to-date that targets VWF. Thus, the AIM is a mechano-regulator of VWF activity. Its conformational dynamics may define the extent of VWF autoinhibition and subsequent activation under force.
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spelling pubmed-80602782021-05-11 Activation of von Willebrand factor via mechanical unfolding of its discontinuous autoinhibitory module Arce, Nicholas A. Cao, Wenpeng Brown, Alexander K. Legan, Emily R. Wilson, Moriah S. Xu, Emma-Ruoqi Berndt, Michael C. Emsley, Jonas Zhang, X. Frank Li, Renhao Nat Commun Article Von Willebrand factor (VWF) activates in response to shear flow to initiate hemostasis, while aberrant activation could lead to thrombosis. Above a critical shear force, the A1 domain of VWF becomes activated and captures platelets via the GPIb-IX complex. Here we show that the shear-responsive element controlling VWF activation resides in the discontinuous autoinhibitory module (AIM) flanking A1. Application of tensile force in a single-molecule setting induces cooperative unfolding of the AIM to expose A1. The AIM-unfolding force is lowered by truncating either N- or C-terminal AIM region, type 2B VWD mutations, or binding of a ristocetin-mimicking monoclonal antibody, all of which could activate A1. Furthermore, the AIM is mechanically stabilized by the nanobody that comprises caplacizumab, the only FDA-approved anti-thrombotic drug to-date that targets VWF. Thus, the AIM is a mechano-regulator of VWF activity. Its conformational dynamics may define the extent of VWF autoinhibition and subsequent activation under force. Nature Publishing Group UK 2021-04-21 /pmc/articles/PMC8060278/ /pubmed/33883551 http://dx.doi.org/10.1038/s41467-021-22634-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Arce, Nicholas A.
Cao, Wenpeng
Brown, Alexander K.
Legan, Emily R.
Wilson, Moriah S.
Xu, Emma-Ruoqi
Berndt, Michael C.
Emsley, Jonas
Zhang, X. Frank
Li, Renhao
Activation of von Willebrand factor via mechanical unfolding of its discontinuous autoinhibitory module
title Activation of von Willebrand factor via mechanical unfolding of its discontinuous autoinhibitory module
title_full Activation of von Willebrand factor via mechanical unfolding of its discontinuous autoinhibitory module
title_fullStr Activation of von Willebrand factor via mechanical unfolding of its discontinuous autoinhibitory module
title_full_unstemmed Activation of von Willebrand factor via mechanical unfolding of its discontinuous autoinhibitory module
title_short Activation of von Willebrand factor via mechanical unfolding of its discontinuous autoinhibitory module
title_sort activation of von willebrand factor via mechanical unfolding of its discontinuous autoinhibitory module
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060278/
https://www.ncbi.nlm.nih.gov/pubmed/33883551
http://dx.doi.org/10.1038/s41467-021-22634-x
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