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Allostery and instability in the functional plasticity of synaptotagmin I

Synaptotagmin I (Syt I) is the calcium ion sensor for regulated release of neurotransmitter. How Syt I mediates this cellular event has been a question of extensive study for decades and yet, a clear understanding of the protein’s diverse functionality has remained elusive. Using tools of thermodyna...

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Detalles Bibliográficos
Autores principales: Fealey, Michael E., Hinderliter, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3609835/
https://www.ncbi.nlm.nih.gov/pubmed/23750295
http://dx.doi.org/10.4161/cib.22830
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author Fealey, Michael E.
Hinderliter, Anne
author_facet Fealey, Michael E.
Hinderliter, Anne
author_sort Fealey, Michael E.
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description Synaptotagmin I (Syt I) is the calcium ion sensor for regulated release of neurotransmitter. How Syt I mediates this cellular event has been a question of extensive study for decades and yet, a clear understanding of the protein’s diverse functionality has remained elusive. Using tools of thermodynamics, we have identified two intrinsic properties that may account for Syt I’s functional plasticity: marginal stability and negative coupling. These two intrinsic properties have the potential to provide great conformational flexibility and suggest that Syt I’s functional plasticity stems in part from subtle rearrangements in the protein’s conformational ensemble. This model for Syt I function is discussed within the context of the nervous system’s overall plasticity.
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spelling pubmed-36098352013-06-07 Allostery and instability in the functional plasticity of synaptotagmin I Fealey, Michael E. Hinderliter, Anne Commun Integr Biol Article Addendum Synaptotagmin I (Syt I) is the calcium ion sensor for regulated release of neurotransmitter. How Syt I mediates this cellular event has been a question of extensive study for decades and yet, a clear understanding of the protein’s diverse functionality has remained elusive. Using tools of thermodynamics, we have identified two intrinsic properties that may account for Syt I’s functional plasticity: marginal stability and negative coupling. These two intrinsic properties have the potential to provide great conformational flexibility and suggest that Syt I’s functional plasticity stems in part from subtle rearrangements in the protein’s conformational ensemble. This model for Syt I function is discussed within the context of the nervous system’s overall plasticity. Landes Bioscience 2013-03-01 2013-03-01 /pmc/articles/PMC3609835/ /pubmed/23750295 http://dx.doi.org/10.4161/cib.22830 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Article Addendum
Fealey, Michael E.
Hinderliter, Anne
Allostery and instability in the functional plasticity of synaptotagmin I
title Allostery and instability in the functional plasticity of synaptotagmin I
title_full Allostery and instability in the functional plasticity of synaptotagmin I
title_fullStr Allostery and instability in the functional plasticity of synaptotagmin I
title_full_unstemmed Allostery and instability in the functional plasticity of synaptotagmin I
title_short Allostery and instability in the functional plasticity of synaptotagmin I
title_sort allostery and instability in the functional plasticity of synaptotagmin i
topic Article Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3609835/
https://www.ncbi.nlm.nih.gov/pubmed/23750295
http://dx.doi.org/10.4161/cib.22830
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