3D Mapping of the SPRY2 domain of ryanodine receptor 1 by single-particle cryo-EM.
The type 1 skeletal muscle ryanodine receptor (RyR1) is principally responsible for Ca(2+) release from the sarcoplasmic reticulum and for the subsequent muscle contraction. The RyR1 contains three SPRY domains. SPRY domains are generally known to mediate protein-protein interactions, however the lo...
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doaj-104ae59be1d54bedb1b53b418169fa2a2020-11-25T02:15:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01610e2581310.1371/journal.pone.00258133D Mapping of the SPRY2 domain of ryanodine receptor 1 by single-particle cryo-EM.Alex Perálvarez-MarínHanshen TaePhilip G BoardMarco G CasarottoAngela F DulhuntyMontserrat SamsóThe type 1 skeletal muscle ryanodine receptor (RyR1) is principally responsible for Ca(2+) release from the sarcoplasmic reticulum and for the subsequent muscle contraction. The RyR1 contains three SPRY domains. SPRY domains are generally known to mediate protein-protein interactions, however the location of the three SPRY domains in the 3D structure of the RyR1 is not known. Combining immunolabeling and single-particle cryo-electron microscopy we have mapped the SPRY2 domain (S1085-V1208) in the 3D structure of RyR1 using three different antibodies against the SPRY2 domain. Two obstacles for the image processing procedure; limited amount of data and signal dilution introduced by the multiple orientations of the antibody bound in the tetrameric RyR1, were overcome by modifying the 3D reconstruction scheme. This approach enabled us to ascertain that the three antibodies bind to the same region, to obtain a 3D reconstruction of RyR1 with the antibody bound, and to map SPRY2 to the periphery of the cytoplasmic domain of RyR1. We report here the first 3D localization of a SPRY2 domain in any known RyR isoform.http://europepmc.org/articles/PMC3187800?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alex Perálvarez-Marín Hanshen Tae Philip G Board Marco G Casarotto Angela F Dulhunty Montserrat Samsó |
spellingShingle |
Alex Perálvarez-Marín Hanshen Tae Philip G Board Marco G Casarotto Angela F Dulhunty Montserrat Samsó 3D Mapping of the SPRY2 domain of ryanodine receptor 1 by single-particle cryo-EM. PLoS ONE |
author_facet |
Alex Perálvarez-Marín Hanshen Tae Philip G Board Marco G Casarotto Angela F Dulhunty Montserrat Samsó |
author_sort |
Alex Perálvarez-Marín |
title |
3D Mapping of the SPRY2 domain of ryanodine receptor 1 by single-particle cryo-EM. |
title_short |
3D Mapping of the SPRY2 domain of ryanodine receptor 1 by single-particle cryo-EM. |
title_full |
3D Mapping of the SPRY2 domain of ryanodine receptor 1 by single-particle cryo-EM. |
title_fullStr |
3D Mapping of the SPRY2 domain of ryanodine receptor 1 by single-particle cryo-EM. |
title_full_unstemmed |
3D Mapping of the SPRY2 domain of ryanodine receptor 1 by single-particle cryo-EM. |
title_sort |
3d mapping of the spry2 domain of ryanodine receptor 1 by single-particle cryo-em. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2011-01-01 |
description |
The type 1 skeletal muscle ryanodine receptor (RyR1) is principally responsible for Ca(2+) release from the sarcoplasmic reticulum and for the subsequent muscle contraction. The RyR1 contains three SPRY domains. SPRY domains are generally known to mediate protein-protein interactions, however the location of the three SPRY domains in the 3D structure of the RyR1 is not known. Combining immunolabeling and single-particle cryo-electron microscopy we have mapped the SPRY2 domain (S1085-V1208) in the 3D structure of RyR1 using three different antibodies against the SPRY2 domain. Two obstacles for the image processing procedure; limited amount of data and signal dilution introduced by the multiple orientations of the antibody bound in the tetrameric RyR1, were overcome by modifying the 3D reconstruction scheme. This approach enabled us to ascertain that the three antibodies bind to the same region, to obtain a 3D reconstruction of RyR1 with the antibody bound, and to map SPRY2 to the periphery of the cytoplasmic domain of RyR1. We report here the first 3D localization of a SPRY2 domain in any known RyR isoform. |
url |
http://europepmc.org/articles/PMC3187800?pdf=render |
work_keys_str_mv |
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