Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Wenbo, Kudryashev, Mikhail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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
_version_ 1783529675619827712
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