Ryanodine receptor 1 and its potential gating mechanism: recent progress
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Grade 2013,Clinical Medicine,Second Military Medical University,Shanghai,Grade 2013,Naval Clinical Medicine,Faculty of Naval Medicine,Second Military Medical University,Shanghai,Faculty of Naval Medicine,Second Military Medical University,Shanghai,Department of Marine Biotechnology,Faculty of Naval Medicine,Second Military Medical University,Shanghai

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Supported by National Natural Science Foundation of China (81470518) and Innovation Fund for Students of Second Military Medical University of 2015 (MS2015014, MS2015028).

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    Abstract:

    The ryanodine receptors (RyRs) are intracellular Ca2+ releasing channels on the sarcoplasmic reticulum membrane and play a pivotal role in the excitation-contraction coupling of skeletal and cardiac muscles as well as other physiological processes. With the recent development of Cryo-EM and the improvement of data analysis technique, scientists from China, the United States and Germany have acquired high-quality RyR1 images at the total resolutions of 3.8 Å (1 Å=10-10 m), 4.8 Å and 6.1 Å, respectively, which have been published in the same issue of Nature in 2015. RyR1s are homotetrameric complexes with a molecular mass of more than 2200000, mainly containing a cytoplasmic region composed of NTD, SPRY, P1, P2, B-sol and C-sol domains and a channel region composed of S1-S6, VSL and CTD domains. As the most common factor affecting the condition of RyR1, Ca2+ is able to bind the EF-hand subdomain in the cytoplasmic region, which further causes the conformational change and finally leads to the channel opening.

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History
  • Received:March 15,2016
  • Revised:June 07,2016
  • Adopted:July 07,2016
  • Online: July 27,2016
  • Published:
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