Lipid-mediated gating of a miniature mechanosensitive MscS channel from Trypanosoma cruzi

Abstract The mechanosensitive channel of small conductance (MscS) from E. coli (EcMscS) has served as the prevailing model system for understanding mechanotransduction in ion channels. Trypanosoma cruzi, the protozoan parasite causing Chagas disease, encodes a miniature MscS ortholog (TcMscS) critic...

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Main Authors: Jingying Zhang, Aashish Bhatt, Grigory Maksaev, Yun Lyna Luo, Peng Yuan
Format: Article
Language:English
Published: Nature Portfolio 2025-08-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-025-62757-z
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author Jingying Zhang
Aashish Bhatt
Grigory Maksaev
Yun Lyna Luo
Peng Yuan
author_facet Jingying Zhang
Aashish Bhatt
Grigory Maksaev
Yun Lyna Luo
Peng Yuan
author_sort Jingying Zhang
collection DOAJ
description Abstract The mechanosensitive channel of small conductance (MscS) from E. coli (EcMscS) has served as the prevailing model system for understanding mechanotransduction in ion channels. Trypanosoma cruzi, the protozoan parasite causing Chagas disease, encodes a miniature MscS ortholog (TcMscS) critical for parasite development and infectivity. TcMscS contains a minimal portion of the canonical EcMscS fold yet maintains mechanosensitive channel activity, thus presenting a unique model system to assess the essential molecular determinants underlying mechanotransduction. Using cryo-electron microscopy and molecular dynamics simulations, we show that TcMscS contains two short membrane-embedded helices that would not fully cross an intact lipid bilayer. Consequently, drastic membrane deformation is induced at the protein-lipid interface, resulting in a funnel-shaped bilayer surrounding the channel. Resident lipids within the central pore lumen block ion permeation pathway, and their departure driven by lateral membrane tension is required for ion conduction. Together with electrophysiology and mutagenesis studies, our results support a direct lipid-mediated mechanical gating transition. Moreover, these findings provide a foundation for the development of alternative treatment of Chagas disease by inhibition of the TcMscS channel.
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spelling doaj-art-0000aef5d0f94190ab482cd5899f80c92025-08-20T03:46:11ZengNature PortfolioNature Communications2041-17232025-08-0116111110.1038/s41467-025-62757-zLipid-mediated gating of a miniature mechanosensitive MscS channel from Trypanosoma cruziJingying Zhang0Aashish Bhatt1Grigory Maksaev2Yun Lyna Luo3Peng Yuan4Department of Pharmacological Sciences, Icahn School of Medicine at Mount SinaiDepartment of Biotechnology and Pharmaceutical Sciences, Western University of Health SciencesDepartment of Cell Biology and Physiology, Washington University School of MedicineDepartment of Biotechnology and Pharmaceutical Sciences, Western University of Health SciencesDepartment of Pharmacological Sciences, Icahn School of Medicine at Mount SinaiAbstract The mechanosensitive channel of small conductance (MscS) from E. coli (EcMscS) has served as the prevailing model system for understanding mechanotransduction in ion channels. Trypanosoma cruzi, the protozoan parasite causing Chagas disease, encodes a miniature MscS ortholog (TcMscS) critical for parasite development and infectivity. TcMscS contains a minimal portion of the canonical EcMscS fold yet maintains mechanosensitive channel activity, thus presenting a unique model system to assess the essential molecular determinants underlying mechanotransduction. Using cryo-electron microscopy and molecular dynamics simulations, we show that TcMscS contains two short membrane-embedded helices that would not fully cross an intact lipid bilayer. Consequently, drastic membrane deformation is induced at the protein-lipid interface, resulting in a funnel-shaped bilayer surrounding the channel. Resident lipids within the central pore lumen block ion permeation pathway, and their departure driven by lateral membrane tension is required for ion conduction. Together with electrophysiology and mutagenesis studies, our results support a direct lipid-mediated mechanical gating transition. Moreover, these findings provide a foundation for the development of alternative treatment of Chagas disease by inhibition of the TcMscS channel.https://doi.org/10.1038/s41467-025-62757-z
spellingShingle Jingying Zhang
Aashish Bhatt
Grigory Maksaev
Yun Lyna Luo
Peng Yuan
Lipid-mediated gating of a miniature mechanosensitive MscS channel from Trypanosoma cruzi
Nature Communications
title Lipid-mediated gating of a miniature mechanosensitive MscS channel from Trypanosoma cruzi
title_full Lipid-mediated gating of a miniature mechanosensitive MscS channel from Trypanosoma cruzi
title_fullStr Lipid-mediated gating of a miniature mechanosensitive MscS channel from Trypanosoma cruzi
title_full_unstemmed Lipid-mediated gating of a miniature mechanosensitive MscS channel from Trypanosoma cruzi
title_short Lipid-mediated gating of a miniature mechanosensitive MscS channel from Trypanosoma cruzi
title_sort lipid mediated gating of a miniature mechanosensitive mscs channel from trypanosoma cruzi
url https://doi.org/10.1038/s41467-025-62757-z
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