A dynamic biointerface in mussels mediated by a mechanoresponsive intermediate filament-based biopolymer

Mussels fabricate a distinctive biointerface that bridges their non-living biopolymeric byssus (used for anchoring in seashore habitats) with their soft-living tissue. Occurring in a region known as the byssus stem root, this biointerface is at once strong, yet also capable of on-demand release under apparent neurobiological control by the mussel, but this is not well understood. Here, we identify and sequence a previously unknown intermediate filament protein (MSP-1) that based on immunohistochemical staining and spectroscopic mapping comprises the surface of the stem root in direct contact with billions of motile cilia emerging from the living tissue. Further structural analysis indicates that MSP-1 is secreted as an α-helical coiled-coil but is mechanically converted subsequently to a β-sheet conformation. We posit that this mechanoresponsive conversion has a mechanical function in toughening the interface, but possibly also as a mechanosensory mechanism given its intimate contact with cilia in the living tissue.

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Publication Details

Journal
Nature Communications
Published
2025-10-28
DOI
https://doi.org/10.1038/s41467-025-64527-3
Citations
1
Primary Topic
Polymer Surface Interaction Studies
Type
article
Field-Weighted Citation Impact
0.66

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article

A dynamic biointerface in mussels mediated by a mechanoresponsive intermediate filament-based biopolymer

Jenaes Sivasundarampillai, Franziska Jehle, Daniel J. Jackson, Emily N. P. Prowse et al.
1 citations
Nature Communications
Polymer Surface Interaction Studies
0.66
article

A dynamic biointerface in mussels mediated by a mechanoresponsive intermediate filament-based biopolymer

Jenaes Sivasundarampillai, Franziska Jehle, Daniel J. Jackson, Emily N. P. Prowse, E. Deniz Eren, Lucia Youssef, Adam G. Hendricks, Matthew J. Harrington, Christopher J. Thibodeaux
article en
1 citations

Abstract

Mussels fabricate a distinctive biointerface that bridges their non-living biopolymeric byssus (used for anchoring in seashore habitats) with their soft-living tissue. Occurring in a region known as the byssus stem root, this biointerface is at once strong, yet also capable of on-demand release under apparent neurobiological control by the mussel, but this is not well understood. Here, we identify and sequence a previously unknown intermediate filament protein (MSP-1) that based on immunohistochemical staining and spectroscopic mapping comprises the surface of the stem root in direct contact with billions of motile cilia emerging from the living tissue. Further structural analysis indicates that MSP-1 is secreted as an α-helical coiled-coil but is mechanically converted subsequently to a β-sheet conformation. We posit that this mechanoresponsive conversion has a mechanical function in toughening the interface, but possibly also as a mechanosensory mechanism given its intimate contact with cilia in the living tissue.

Nature CommunicationsVol. 16(1)
Max Planck Institute of Colloids and Interfaces (DE), McGill University (CA), University of Göttingen (DE)
McGill University, McGill University Health Centre, Deutsche Forschungsgemeinschaft, Max-Planck-Gesellschaft, Canadian Institutes of Health Research, Natural Sciences and Engineering Research Council of Canada, Fonds de recherche du Québec – Nature et technologies
Openalex Percentile: Top 26%
Polymer Surface Interaction Studies
0.66
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