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Design of a Photoswitchable Cadherin

[Image: see text] There is a growing interest in engineering proteins whose function can be controlled with the spatial and temporal precision of light. Here, we present a novel example of a functional light-triggered switch in the Ca-dependent cell–cell adhesion protein E-cadherin, created using a...

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Autores principales: Ritterson, Ryan S., Kuchenbecker, Kristopher M., Michalik, Michael, Kortemme, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774674/
https://www.ncbi.nlm.nih.gov/pubmed/23923816
http://dx.doi.org/10.1021/ja404992r
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author Ritterson, Ryan S.
Kuchenbecker, Kristopher M.
Michalik, Michael
Kortemme, Tanja
author_facet Ritterson, Ryan S.
Kuchenbecker, Kristopher M.
Michalik, Michael
Kortemme, Tanja
author_sort Ritterson, Ryan S.
collection PubMed
description [Image: see text] There is a growing interest in engineering proteins whose function can be controlled with the spatial and temporal precision of light. Here, we present a novel example of a functional light-triggered switch in the Ca-dependent cell–cell adhesion protein E-cadherin, created using a mechanism-based design strategy. We report an 18-fold change in apparent Ca(2+) binding affinity upon illumination. Our results include a detailed examination of functional switching via linked changes in Ca(2+) binding and cadherin dimerization. This design opens avenues toward controllable tools that could be applied to many long-standing questions about cadherin’s biological function in cell–cell adhesion and downstream signaling.
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spelling pubmed-37746742013-09-18 Design of a Photoswitchable Cadherin Ritterson, Ryan S. Kuchenbecker, Kristopher M. Michalik, Michael Kortemme, Tanja J Am Chem Soc [Image: see text] There is a growing interest in engineering proteins whose function can be controlled with the spatial and temporal precision of light. Here, we present a novel example of a functional light-triggered switch in the Ca-dependent cell–cell adhesion protein E-cadherin, created using a mechanism-based design strategy. We report an 18-fold change in apparent Ca(2+) binding affinity upon illumination. Our results include a detailed examination of functional switching via linked changes in Ca(2+) binding and cadherin dimerization. This design opens avenues toward controllable tools that could be applied to many long-standing questions about cadherin’s biological function in cell–cell adhesion and downstream signaling. American Chemical Society 2013-08-07 2013-08-28 /pmc/articles/PMC3774674/ /pubmed/23923816 http://dx.doi.org/10.1021/ja404992r Text en Copyright © 2013 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Ritterson, Ryan S.
Kuchenbecker, Kristopher M.
Michalik, Michael
Kortemme, Tanja
Design of a Photoswitchable Cadherin
title Design of a Photoswitchable Cadherin
title_full Design of a Photoswitchable Cadherin
title_fullStr Design of a Photoswitchable Cadherin
title_full_unstemmed Design of a Photoswitchable Cadherin
title_short Design of a Photoswitchable Cadherin
title_sort design of a photoswitchable cadherin
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774674/
https://www.ncbi.nlm.nih.gov/pubmed/23923816
http://dx.doi.org/10.1021/ja404992r
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