Mussels Fabricate Porous Glues via Multiphase Liquid-Liquid Phase Separation of Condensates ARTICLE

被引:17
|
作者
Renner-Rao, Max [1 ]
Jehle, Franziska [1 ,2 ]
Priemel, Tobias [1 ]
Duthoo, Emilie [1 ,3 ]
Fratzl, Peter [2 ]
Bertinetti, Luca [2 ,4 ]
Harrington, Matthew J. [1 ]
机构
[1] McGill Univ, Dept Chem, Montreal, PQ H4A 0B8, Canada
[2] Max Planck Inst Colloids & Interfaces, Dept Biomat, D-14476 Potsdam, Germany
[3] Res Inst Biosci, Biol Marine Organisms & Biomimet Unit, B-7000 Mons, Belgium
[4] Tech Univ Dresden, B CUBE Ctr Mol Bioengn, D-01307 Dresden, Germany
基金
加拿大自然科学与工程研究理事会;
关键词
protein condensates; liquid-liquid phase separation (LLPS); mussel byssus; adhesion; self-assembly; coacervation; ATTACHMENT PLAQUE; SULFATE UPTAKE; ADHESIVE; PROTEINS; PH; COACERVATION; MECHANICS; REPAIR;
D O I
10.1021/acsnano.2c08410
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mussels (Mytilus edulis) adhere to hard surfaces in intertidal marine habitats with a porous underwater glue called the byssus plaque. The plaque is an established role model for bioinspired underwater glues and comprises at least six proteins, most of which are highly cationic and enriched in the post-translationally modified amino acid 3,4-dihydroxyphenylalanine (DOPA). While much is known about the chemistry of plaque adhesion, less is understood about the natural plaque formation process. Here, we investigated plaque structure and formation using 3D electron microscopic imaging, revealing that micro-and nanopores form spontaneously during secretion of protein-filled secretory vesicles. To better understand this process, we developed a method to purify intact secretory vesicles for in vitro assembly studies. We discovered that each vesicle contains a sulfate-associated fluid condensate consisting of similar to 9 histidine-and/or DOPA-rich proteins, which are presumably the required ingredients for building a plaque. Rupturing vesicles under specific buffering conditions relevant for natural assembly led to controlled multiphase liquid-liquid phase separation (LLPS) of different proteins, resulting in formation of a continuous phase with coexisting droplets. Rapid coarsening of the droplet phase was arrested through pH-dependent cross-linking of the continuous phase, producing native like solid porous "microplaques" with droplet proteins remaining as fluid condensates within the pores. Results indicate that histidine deprotonation and sulfates figure prominently in condensate cross-linking. Distilled concepts suggest that combining phase separation with tunable cross-linking kinetics could be effective for microfabricating hierarchically porous materials via self-assembly.
引用
收藏
页码:20877 / 20890
页数:14
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