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Molecular structure and conformation of stereocilia tip-links elucidated by cryo-electron tomography

View ORCID ProfileJohannes Elferich, View ORCID ProfileSarah Clark, View ORCID ProfileJingpeng Ge, View ORCID ProfileApril Goehring, View ORCID ProfileAya Matsui, View ORCID ProfileEric Gouaux
doi: https://doi.org/10.1101/2021.10.01.462800
Johannes Elferich
1Vollum Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239
2RNA Therapeutics Institute, UMass Chan Medical School, 368 Plantation St, Worcester, MA 01605
3Howard Hughes Medical Institute, Portland, OR 97239
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  • ORCID record for Johannes Elferich
Sarah Clark
1Vollum Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239
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Jingpeng Ge
1Vollum Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239
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April Goehring
1Vollum Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239
3Howard Hughes Medical Institute, Portland, OR 97239
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Aya Matsui
1Vollum Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239
3Howard Hughes Medical Institute, Portland, OR 97239
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Eric Gouaux
1Vollum Institute, Oregon Health & Science University, 3181 SW Sam Jackson Park Road, Portland, OR 97239
3Howard Hughes Medical Institute, Portland, OR 97239
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  • For correspondence: gouauxe@ohsu.edu
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Abstract

Mechanosensory transduction (MT), the conversion of mechanical stimuli into electrical signals, underpins hearing and balance and is carried out within hair cells in the inner ear. Hair cells harbor actin-filled stereocilia, arranged in rows of descending heights, where the tips of stereocilia are connected to their taller neighbors by a filament composed of protocadherin 15 (PCDH15) and cadherin 23 (CDH23), deemed the ‘tip-link’. Tension exerted on the tip-link opens an ion channel at the tip of the shorter stereocilia, thus converting mechanical force into an electrical signal. While biochemical and structural studies have provided insights into the molecular composition and structure of isolated portions of the tip-link, the architecture, location and conformational states of intact tip-links, on stereocilia, remains unknown. Here we report in situ cryo-electron microscopy imaging of the tip-link in mouse stereocilia. We observe individual PCDH15 molecules at the tip and shaft of stereocilia and determine their stoichiometry, conformational heterogeneity, and their complexes with CDH23. The PCDH15/CDH23 complexes occur in clusters, frequently with more than one copy of PCDH15 at the tip of stereocilia, suggesting that tip-links might consist of more than one copy of the PCDH15/CDH23 heterotetramer and by extension, might include multiple MT complexes.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • ↵4 Lead contact

  • https://figshare.com/articles/media/Movies_of_tomograms_containing_PCDH15_molecules_stained_with_39G7-AuNP/16725199

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted October 01, 2021.
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Molecular structure and conformation of stereocilia tip-links elucidated by cryo-electron tomography
Johannes Elferich, Sarah Clark, Jingpeng Ge, April Goehring, Aya Matsui, Eric Gouaux
bioRxiv 2021.10.01.462800; doi: https://doi.org/10.1101/2021.10.01.462800
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Molecular structure and conformation of stereocilia tip-links elucidated by cryo-electron tomography
Johannes Elferich, Sarah Clark, Jingpeng Ge, April Goehring, Aya Matsui, Eric Gouaux
bioRxiv 2021.10.01.462800; doi: https://doi.org/10.1101/2021.10.01.462800

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