The mechanosensitive Piezo1 channel: a three‐bladed propeller‐like structure and a lever‐like mechanogating mechanism. (14th December 2018)
- Record Type:
- Journal Article
- Title:
- The mechanosensitive Piezo1 channel: a three‐bladed propeller‐like structure and a lever‐like mechanogating mechanism. (14th December 2018)
- Main Title:
- The mechanosensitive Piezo1 channel: a three‐bladed propeller‐like structure and a lever‐like mechanogating mechanism
- Authors:
- Zhao, Qiancheng
Zhou, Heng
Li, Xueming
Xiao, Bailong - Abstract:
- Abstract : The evolutionarily conserved Piezo proteins, including Piezo1 and Piezo2, constitute a bona fide class of mechanosensitive (MS) cation channels, which play critical roles in various mammalian physiologies, including sensation of touch, proprioception and regulation of vascular development, and blood pressure. Furthermore, mutations in Piezos have been linked to various human genetic diseases, validating their potential as therapeutic targets. Thus, it is pivotal to understand how Piezo channels effectively convert mechanical force into selective cation permeation, and therefore precisely control the various mechanotransduction processes. On the basis of our recently determined cryoelectron microscopy structures of the full‐length 2547‐residue mouse Piezo1, structure‐guided mutagenesis, and electrophysiological and pharmacological characterizations, here we focus on reviewing the key structural features and functional components that enable Piezo1 to employ a lever‐like mechanogating mechanism to function as a sophisticated mechanotransduction channel. Abstract : The mechanosensitive Piezo1 channel possesses a 38‐TM topology model and forms a unique three‐bladed, propeller‐like structure comprising three structural and functional modules: the TM‐blade‐constituted mechanosensing module that consists of nine repetitive transmembrane helical units (THUs), the C‐terminal ion‐conducting pore module, and the transduction module including the beam, anchor, and CTD. TheAbstract : The evolutionarily conserved Piezo proteins, including Piezo1 and Piezo2, constitute a bona fide class of mechanosensitive (MS) cation channels, which play critical roles in various mammalian physiologies, including sensation of touch, proprioception and regulation of vascular development, and blood pressure. Furthermore, mutations in Piezos have been linked to various human genetic diseases, validating their potential as therapeutic targets. Thus, it is pivotal to understand how Piezo channels effectively convert mechanical force into selective cation permeation, and therefore precisely control the various mechanotransduction processes. On the basis of our recently determined cryoelectron microscopy structures of the full‐length 2547‐residue mouse Piezo1, structure‐guided mutagenesis, and electrophysiological and pharmacological characterizations, here we focus on reviewing the key structural features and functional components that enable Piezo1 to employ a lever‐like mechanogating mechanism to function as a sophisticated mechanotransduction channel. Abstract : The mechanosensitive Piezo1 channel possesses a 38‐TM topology model and forms a unique three‐bladed, propeller‐like structure comprising three structural and functional modules: the TM‐blade‐constituted mechanosensing module that consists of nine repetitive transmembrane helical units (THUs), the C‐terminal ion‐conducting pore module, and the transduction module including the beam, anchor, and CTD. The THU‐beam‐structure constitutes a lever‐like transduction pathway for long‐distance chemical‐ and mechanical gating of Piezo1. … (more)
- Is Part Of:
- FEBS journal. Volume 286:Number 13(2019)
- Journal:
- FEBS journal
- Issue:
- Volume 286:Number 13(2019)
- Issue Display:
- Volume 286, Issue 13 (2019)
- Year:
- 2019
- Volume:
- 286
- Issue:
- 13
- Issue Sort Value:
- 2019-0286-0013-0000
- Page Start:
- 2461
- Page End:
- 2470
- Publication Date:
- 2018-12-14
- Subjects:
- cryo‐EM structure -- ion permeation -- lever -- mechanogating -- mechanotransduction -- Piezo channel -- pore
Biochemistry -- Periodicals
Molecular biology -- Periodicals
Pathology, Molecular -- Periodicals
572 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&NEWS=n&PAGE=toc&D=ovft&AN=01038983-000000000-00000 ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=ejb ↗
http://onlinelibrary.wiley.com/ ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=ejb ↗ - DOI:
- 10.1111/febs.14711 ↗
- Languages:
- English
- ISSNs:
- 1742-464X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3901.578500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11031.xml