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Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission

Neural networks are optimized to detect temporal coincidence on the millisecond timescale. Here, we offer a synthetic hypothesis based on recent structural insights into SNAREs and the C2 domain proteins to explain how synaptic transmission can keep this pace. We suggest that an outer ring of up to...

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Autores principales: Rothman, James E., Krishnakumar, Shyam S., Grushin, Kirill, Pincet, Frederic
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698743/
https://www.ncbi.nlm.nih.gov/pubmed/28983915
http://dx.doi.org/10.1002/1873-3468.12874
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author Rothman, James E.
Krishnakumar, Shyam S.
Grushin, Kirill
Pincet, Frederic
author_facet Rothman, James E.
Krishnakumar, Shyam S.
Grushin, Kirill
Pincet, Frederic
author_sort Rothman, James E.
collection PubMed
description Neural networks are optimized to detect temporal coincidence on the millisecond timescale. Here, we offer a synthetic hypothesis based on recent structural insights into SNAREs and the C2 domain proteins to explain how synaptic transmission can keep this pace. We suggest that an outer ring of up to six curved Munc13 ‘MUN’ domains transiently anchored to the plasma membrane via its flanking domains surrounds a stable inner ring comprised of synaptotagmin C2 domains to serve as a work‐bench on which SNAREpins are templated. This ‘buttressed‐ring hypothesis’ affords straightforward answers to many principal and long‐standing questions concerning how SNAREpins can be assembled, clamped, and then released synchronously with an action potential.
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spelling pubmed-56987432017-11-30 Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission Rothman, James E. Krishnakumar, Shyam S. Grushin, Kirill Pincet, Frederic FEBS Lett Hypothesis Neural networks are optimized to detect temporal coincidence on the millisecond timescale. Here, we offer a synthetic hypothesis based on recent structural insights into SNAREs and the C2 domain proteins to explain how synaptic transmission can keep this pace. We suggest that an outer ring of up to six curved Munc13 ‘MUN’ domains transiently anchored to the plasma membrane via its flanking domains surrounds a stable inner ring comprised of synaptotagmin C2 domains to serve as a work‐bench on which SNAREpins are templated. This ‘buttressed‐ring hypothesis’ affords straightforward answers to many principal and long‐standing questions concerning how SNAREpins can be assembled, clamped, and then released synchronously with an action potential. John Wiley and Sons Inc. 2017-10-31 2017-11 /pmc/articles/PMC5698743/ /pubmed/28983915 http://dx.doi.org/10.1002/1873-3468.12874 Text en © 2017 The Authors. FEBS Letters published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Hypothesis
Rothman, James E.
Krishnakumar, Shyam S.
Grushin, Kirill
Pincet, Frederic
Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission
title Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission
title_full Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission
title_fullStr Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission
title_full_unstemmed Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission
title_short Hypothesis – buttressed rings assemble, clamp, and release SNAREpins for synaptic transmission
title_sort hypothesis – buttressed rings assemble, clamp, and release snarepins for synaptic transmission
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698743/
https://www.ncbi.nlm.nih.gov/pubmed/28983915
http://dx.doi.org/10.1002/1873-3468.12874
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