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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2013
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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. |
format | Online Article Text |
id | pubmed-3774674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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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