EMD-7042

Single-particle
3.8 Å
EMD-7042 Deposition: 22/09/2017
Map released: 20/12/2017
Last modified: 23/10/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links

EMD-7042

Structure of the mechanosensitive channel Piezo1

EMD-7042

Single-particle
3.8 Å
EMD-7042 Deposition: 22/09/2017
Map released: 20/12/2017
Last modified: 23/10/2024
Overview 3D View Sample Experiment Validation Volume Browser Additional data Links
Sample Organism: Mus musculus
Sample: mouse Piezo1 channel
Fitted models: 6b3r (Avg. Q-score: 0.236)

Deposition Authors: Guo YR , MacKinnon R
Structure-based membrane dome mechanism for Piezo mechanosensitivity.
Guo YR , MacKinnon R
(2017) eLife , 6
PUBMED: 29231809
DOI: doi:10.7554/eLife.33660
ISSN: 2050-084X
Abstract:
Mechanosensitive ion channels convert external mechanical stimuli into electrochemical signals for critical processes including touch sensation, balance, and cardiovascular regulation. The best understood mechanosensitive channel, MscL, opens a wide pore, which accounts for mechanosensitive gating due to in-plane area expansion. Eukaryotic Piezo channels have a narrow pore and therefore must capture mechanical forces to control gating in another way. We present a cryo-EM structure of mouse Piezo1 in a closed conformation at 3.7Å-resolution. The channel is a triskelion with arms consisting of repeated arrays of 4-TM structural units surrounding a pore. Its shape deforms the membrane locally into a dome. We present a hypothesis in which the membrane deformation changes upon channel opening. Quantitatively, membrane tension will alter gating energetics in proportion to the change in projected area under the dome. This mechanism can account for highly sensitive mechanical gating in the setting of a narrow, cation-selective pore.