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Structure of RyR1 in native membranes
Ryanodine receptor 1 (RyR1) mediates excitation–contraction coupling by releasing Ca(2+) from sarcoplasmic reticulum (SR) to the cytoplasm of skeletal muscle cells. RyR1 activation is regulated by several proteins from both the cytoplasm and lumen of the SR. Here, we report the structure of RyR1 fro...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202208/ https://www.ncbi.nlm.nih.gov/pubmed/32147968 http://dx.doi.org/10.15252/embr.201949891 |
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author | Chen, Wenbo Kudryashev, Mikhail |
author_facet | Chen, Wenbo Kudryashev, Mikhail |
author_sort | Chen, Wenbo |
collection | PubMed |
description | Ryanodine receptor 1 (RyR1) mediates excitation–contraction coupling by releasing Ca(2+) from sarcoplasmic reticulum (SR) to the cytoplasm of skeletal muscle cells. RyR1 activation is regulated by several proteins from both the cytoplasm and lumen of the SR. Here, we report the structure of RyR1 from native SR membranes in closed and open states. Compared to the previously reported structures of purified RyR1, our structure reveals helix‐like densities traversing the bilayer approximately 5 nm from the RyR1 transmembrane domain and sarcoplasmic extensions linking RyR1 to a putative calsequestrin network. We document the primary conformation of RyR1 in situ and its structural variations. The activation of RyR1 is associated with changes in membrane curvature and movement in the sarcoplasmic extensions. Our results provide structural insight into the mechanism of RyR1 in its native environment. |
format | Online Article Text |
id | pubmed-7202208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72022082020-05-07 Structure of RyR1 in native membranes Chen, Wenbo Kudryashev, Mikhail EMBO Rep Reports Ryanodine receptor 1 (RyR1) mediates excitation–contraction coupling by releasing Ca(2+) from sarcoplasmic reticulum (SR) to the cytoplasm of skeletal muscle cells. RyR1 activation is regulated by several proteins from both the cytoplasm and lumen of the SR. Here, we report the structure of RyR1 from native SR membranes in closed and open states. Compared to the previously reported structures of purified RyR1, our structure reveals helix‐like densities traversing the bilayer approximately 5 nm from the RyR1 transmembrane domain and sarcoplasmic extensions linking RyR1 to a putative calsequestrin network. We document the primary conformation of RyR1 in situ and its structural variations. The activation of RyR1 is associated with changes in membrane curvature and movement in the sarcoplasmic extensions. Our results provide structural insight into the mechanism of RyR1 in its native environment. John Wiley and Sons Inc. 2020-03-09 2020-05-06 /pmc/articles/PMC7202208/ /pubmed/32147968 http://dx.doi.org/10.15252/embr.201949891 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the 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 | Reports Chen, Wenbo Kudryashev, Mikhail Structure of RyR1 in native membranes |
title | Structure of RyR1 in native membranes |
title_full | Structure of RyR1 in native membranes |
title_fullStr | Structure of RyR1 in native membranes |
title_full_unstemmed | Structure of RyR1 in native membranes |
title_short | Structure of RyR1 in native membranes |
title_sort | structure of ryr1 in native membranes |
topic | Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7202208/ https://www.ncbi.nlm.nih.gov/pubmed/32147968 http://dx.doi.org/10.15252/embr.201949891 |
work_keys_str_mv | AT chenwenbo structureofryr1innativemembranes AT kudryashevmikhail structureofryr1innativemembranes |