TY - JOUR
T1 - Structural mechanism for gating of a eukaryotic mechanosensitive channel of small conductance
AU - Deng, Zengqin
AU - Maksaev, Grigory
AU - Schlegel, Angela M.
AU - Zhang, Jingying
AU - Rau, Michael
AU - Fitzpatrick, James A.J.
AU - Haswell, Elizabeth S.
AU - Yuan, Peng
N1 - Funding Information:
This work was supported by start-up funds from Washington University School of Medicine (to P.Y.) and an HHMI-Simons Faculty Scholar Grant to E.S.H. M.R and J.A.J. F are supported by the Washington University Center for Cellular Imaging, which is funded, in part by Washington University School of Medicine, the Children’s Discovery Institute of Washington University and St. Louis Children’s Hospital (CDI-CORE-2015-505 and CDI-CORE-2019-813) and the Foundation for Barnes-Jewish Hospital (3770). A.M.S. is supported by funding from the Spencer T. and Ann W. Olin Fellowship for Women in Graduate Study and the William H. Danforth Plant Sciences Fellowship.
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - Mechanosensitive ion channels transduce physical force into electrochemical signaling that underlies an array of fundamental physiological processes, including hearing, touch, proprioception, osmoregulation, and morphogenesis. The mechanosensitive channels of small conductance (MscS) constitute a remarkably diverse superfamily of channels critical for management of osmotic pressure. Here, we present cryo-electron microscopy structures of a MscS homolog from Arabidopsis thaliana, MSL1, presumably in both the closed and open states. The heptameric MSL1 channel contains an unusual bowl-shaped transmembrane region, which is reminiscent of the evolutionarily and architecturally unrelated mechanosensitive Piezo channels. Upon channel opening, the curved transmembrane domain of MSL1 flattens and expands. Our structures, in combination with functional analyses, delineate a structural mechanism by which mechanosensitive channels open under increased membrane tension. Further, the shared structural feature between unrelated channels suggests the possibility of a unified mechanical gating mechanism stemming from membrane deformation induced by a non-planar transmembrane domain.
AB - Mechanosensitive ion channels transduce physical force into electrochemical signaling that underlies an array of fundamental physiological processes, including hearing, touch, proprioception, osmoregulation, and morphogenesis. The mechanosensitive channels of small conductance (MscS) constitute a remarkably diverse superfamily of channels critical for management of osmotic pressure. Here, we present cryo-electron microscopy structures of a MscS homolog from Arabidopsis thaliana, MSL1, presumably in both the closed and open states. The heptameric MSL1 channel contains an unusual bowl-shaped transmembrane region, which is reminiscent of the evolutionarily and architecturally unrelated mechanosensitive Piezo channels. Upon channel opening, the curved transmembrane domain of MSL1 flattens and expands. Our structures, in combination with functional analyses, delineate a structural mechanism by which mechanosensitive channels open under increased membrane tension. Further, the shared structural feature between unrelated channels suggests the possibility of a unified mechanical gating mechanism stemming from membrane deformation induced by a non-planar transmembrane domain.
UR - http://www.scopus.com/inward/record.url?scp=85088397411&partnerID=8YFLogxK
U2 - 10.1038/s41467-020-17538-1
DO - 10.1038/s41467-020-17538-1
M3 - Article
C2 - 32704140
AN - SCOPUS:85088397411
SN - 2041-1723
VL - 11
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 3690
ER -