Conformational changes upon pore blocker removal reveal conductive states of TMEM16A
Christina Alexandra StephensiD, Frank V. MarcolineiD, Christian J. PetersiD, Michael GrabeiD
Abstract
TMEM16A is a Ca2+-activated anion channel that provides direct electrical feedback to the plasma membrane in response to intracellular Ca2+. Its conductive state remains unresolved, leaving questions about gating, Cl- permeation, and modulation by Ca2+, depolarization, and lipids. To investigate the open state, we performed molecular dynamics simulations of TMEM16A bound to the putative open-state blocker 1PBC. After inhibitor removal, the putative, pore-lining helix TM4 developed kinks at two sites: an upper site that opens the pore for Cl- permeation, and a deeper site causing constriction. A conserved hydrophobic network between TM3 and TM4 persisted in most open structures but separated during extreme dilation, allowing lipids to transiently block the pore. Patch-clamp recordings indicated that the intact network promotes activation. Further simulations yielded >60 Cl- permeation events and a single-channel conductance matching experiments. Additional electrostatic and kinetic modeling indicated that TMEM16As transition from outward-rectification to Ohmic conductance with increasing Ca2+ results from a weak voltage dependence of Ca2+ binding, which act cooperatively to open the pore. HIGHLIGHTSO_LIRemoval of the inhibitor 1PBC from TMEM16A induces spontaneous transitions to ion conductive and non-conductive states via bending in TM4 at two different locations. C_LIO_LISimulations suggest that the open state is stabilized by a small hydrophobic network between TM3 and 4 and disrupting this network biases channel closure in electrophysiological recordings. C_LIO_LIA kinetic model of conduction based on energetics from the all-atom MD simulations coupled to continuum calculations gives a linear current-voltage curve consistent with the fully open conformation and removal of 1 Ca2+ switches to an outwardly rectifying state via electrostatic influence on the Cl- energy profile. However, the rectification is too weak to match experiment, but a cooperative model of Ca2+ binding with weak voltage-dependence does match experiment. C_LI
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- FWCI
- 2.09
- Field percentile
- top 11%
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Specific PIP2 Binding Promotes Calcium Activation of TMEM16A Chloride Channels
Z. Jia, J. Chen·Communications BiologyPeer-reviewed·Feb 26, 2021
- Accessing pore-blocker bound and alternative conductive conformations of TMEM16A using PIP2-assisted adaptive sampling
Tanadet Pipatpolkai, Ee Hou Yong·bioRxiv·Aug 5, 2026
- Orthosteric interactions with PIP2 activate TMEM16A channels
Jimin Xu, Ana Santa Cruz, … Leigh Daniel Plant·bioRxiv·Feb 24, 2025
- PIP2 and Ca2+ regulation of TMEM16A currents in excised inside-out patches
M. Tembo, C. Lara-Santos, … A. E. Carlson·bioRxiv·Aug 30, 2022
- Distinct modulation of calcium-activated chloride channel TMEM16A by a novel drug-binding site
- Dynamic Change of Electrostatic Field in TMEM16F Permeation Pathway Shifts Its Ion Selectivity