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Main Authors: Rivard, Mathieu D, Poulhazan, Alexandre, Renner-Rao, Max J, Duthoo, Emilie, Jehle, Franziska, Flammang, Patrick, Jackson, Daniel J, Harrington, Matthew J
Format: Artículo científico
Language:en
Published: Nature communications 2026
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/41692796/
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author Rivard, Mathieu D
Poulhazan, Alexandre
Renner-Rao, Max J
Duthoo, Emilie
Jehle, Franziska
Flammang, Patrick
Jackson, Daniel J
Harrington, Matthew J
author_facet Rivard, Mathieu D
Poulhazan, Alexandre
Renner-Rao, Max J
Duthoo, Emilie
Jehle, Franziska
Flammang, Patrick
Jackson, Daniel J
Harrington, Matthew J
Rivard, Mathieu D
Poulhazan, Alexandre
Renner-Rao, Max J
Duthoo, Emilie
Jehle, Franziska
Flammang, Patrick
Jackson, Daniel J
Harrington, Matthew J
collection PubMed - marine biology
contents Histidine-rich coiled-coils promote zinc-dependent self-assembly and curing of porous mussel glues. Rivard, Mathieu D Poulhazan, Alexandre Renner-Rao, Max J Duthoo, Emilie Jehle, Franziska Flammang, Patrick Jackson, Daniel J Harrington, Matthew J Animals Zinc Adhesives Bivalvia Porosity Histidine Proteins Amino Acid Sequence Dihydroxyphenylalanine Hydrogen-Ion Concentration Phase Separation Challenging to engineer in synthetic glues, wet adhesion is critical for many technical and biomedical applications. Mussels, however, have evolved underwater glues that adhere effectively onto slippery seashore surfaces. Past research on mussel adhesion highlights the importance of the post-translationally modified amino acid 3,4-dihydroxyphenylalanine (DOPA), found in abundance in mussel glue proteins. Yet, DOPA alone is insufficient to match native adhesion in synthetic mimics. Here, we provide evidence that a previously uncharacterized histidine-rich protein (mefp-12) plays a crucial role in the formation, curing, and performance of mussel glue. Biochemical analysis localizes mefp-12 within vesicles of the mussel glue secretory glands, while AI-assisted modeling of its sequence predicts Zn-stabilized coiled coil conformation and several domains resembling zinc-finger motifs. In vitro investigation of a His-rich α-helical peptide from mefp-12 shows Zn- and pH-dependent liquid-liquid phase separation (LLPS), coalescence, and spreading over the substrate. Exposure to seawater pH induces subsequent self-organization of the fluid condensates into solid nanoporous networks resembling the structure of the native mussel glue. Based on these findings we gain a deeper mechanistic understanding of mussel glue formation and function that challenges the dominant DOPA-centric paradigm, providing inspiration for design of bio-inspired wet adhesives.
format Artículo científico
id pubmed_41692796
institution PubMed
language en
publishDate 2026
publisher Nature communications
record_format pubmed
spellingShingle Histidine-rich coiled-coils promote zinc-dependent self-assembly and curing of porous mussel glues.
Rivard, Mathieu D
Poulhazan, Alexandre
Renner-Rao, Max J
Duthoo, Emilie
Jehle, Franziska
Flammang, Patrick
Jackson, Daniel J
Harrington, Matthew J
Animals
Zinc
Adhesives
Bivalvia
Porosity
Histidine
Proteins
Amino Acid Sequence
Dihydroxyphenylalanine
Hydrogen-Ion Concentration
Phase Separation
Histidine-rich coiled-coils promote zinc-dependent self-assembly and curing of porous mussel glues. Rivard, Mathieu D Poulhazan, Alexandre Renner-Rao, Max J Duthoo, Emilie Jehle, Franziska Flammang, Patrick Jackson, Daniel J Harrington, Matthew J Animals Zinc Adhesives Bivalvia Porosity Histidine Proteins Amino Acid Sequence Dihydroxyphenylalanine Hydrogen-Ion Concentration Phase Separation Challenging to engineer in synthetic glues, wet adhesion is critical for many technical and biomedical applications. Mussels, however, have evolved underwater glues that adhere effectively onto slippery seashore surfaces. Past research on mussel adhesion highlights the importance of the post-translationally modified amino acid 3,4-dihydroxyphenylalanine (DOPA), found in abundance in mussel glue proteins. Yet, DOPA alone is insufficient to match native adhesion in synthetic mimics. Here, we provide evidence that a previously uncharacterized histidine-rich protein (mefp-12) plays a crucial role in the formation, curing, and performance of mussel glue. Biochemical analysis localizes mefp-12 within vesicles of the mussel glue secretory glands, while AI-assisted modeling of its sequence predicts Zn-stabilized coiled coil conformation and several domains resembling zinc-finger motifs. In vitro investigation of a His-rich α-helical peptide from mefp-12 shows Zn- and pH-dependent liquid-liquid phase separation (LLPS), coalescence, and spreading over the substrate. Exposure to seawater pH induces subsequent self-organization of the fluid condensates into solid nanoporous networks resembling the structure of the native mussel glue. Based on these findings we gain a deeper mechanistic understanding of mussel glue formation and function that challenges the dominant DOPA-centric paradigm, providing inspiration for design of bio-inspired wet adhesives.
title Histidine-rich coiled-coils promote zinc-dependent self-assembly and curing of porous mussel glues.
topic Animals
Zinc
Adhesives
Bivalvia
Porosity
Histidine
Proteins
Amino Acid Sequence
Dihydroxyphenylalanine
Hydrogen-Ion Concentration
Phase Separation
url https://pubmed.ncbi.nlm.nih.gov/41692796/