Complexes of vertebrate TMC1/2 and CIB2/3 proteins form hair-cell mechanotransduction cation channels

Bibliographic Details
Title: Complexes of vertebrate TMC1/2 and CIB2/3 proteins form hair-cell mechanotransduction cation channels
Authors: Arnaud PJ Giese, Wei-Hsiang Weng, Katie S Kindt, Hui Ho Vanessa Chang, Jonathan S Montgomery, Evan M Ratzan, Alisha J Beirl, Roberto Aponte Rivera, Jeffrey M Lotthammer, Sanket Walujkar, Mark P Foster, Omid A Zobeiri, Jeffrey R Holt, Saima Riazuddin, Kathleen E Cullen, Marcos Sotomayor, Zubair M Ahmed
Source: eLife, Vol 12 (2025)
Publisher Information: eLife Sciences Publications Ltd, 2025.
Publication Year: 2025
Collection: LCC:Medicine
LCC:Science
LCC:Biology (General)
Subject Terms: zebrafish, CIB2, CIB3, mechanotransduction, TMC1, TMC2, Medicine, Science, Biology (General), QH301-705.5
More Details: Calcium and integrin-binding protein 2 (CIB2) and CIB3 bind to transmembrane channel-like 1 (TMC1) and TMC2, the pore-forming subunits of the inner-ear mechano-electrical transduction (MET) apparatus. These interactions have been proposed to be functionally relevant across mechanosensory organs and vertebrate species. Here, we show that both CIB2 and CIB3 can form heteromeric complexes with TMC1 and TMC2 and are integral for MET function in mouse cochlea and vestibular end organs as well as in zebrafish inner ear and lateral line. Our AlphaFold 2 models suggest that vertebrate CIB proteins can simultaneously interact with at least two cytoplasmic domains of TMC1 and TMC2 as validated using nuclear magnetic resonance spectroscopy of TMC1 fragments interacting with CIB2 and CIB3. Molecular dynamics simulations of TMC1/2 complexes with CIB2/3 predict that TMCs are structurally stabilized by CIB proteins to form cation channels. Overall, our work demonstrates that intact CIB2/3 and TMC1/2 complexes are integral to hair-cell MET function in vertebrate mechanosensory epithelia.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2050-084X
Relation: https://elifesciences.org/articles/89719; https://doaj.org/toc/2050-084X
DOI: 10.7554/eLife.89719
Access URL: https://doaj.org/article/85e19829aa7c4297a417d83991f2bdda
Accession Number: edsdoj.85e19829aa7c4297a417d83991f2bdda
Database: Directory of Open Access Journals
More Details
ISSN:2050084X
DOI:10.7554/eLife.89719
Published in:eLife
Language:English