Peptide-Based Coacervate-Core Vesicles with Semipermeable Membranes

© 2021 The Authors. Advanced Materials published by Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 34(2022), 34 vom: 07. Aug., Seite e2202913
1. Verfasser: Abbas, Manzar (VerfasserIn)
Weitere Verfasser: Law, Jack O, Grellscheid, Sushma N, Huck, Wilhelm T S, Spruijt, Evan
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article coacervate-core vesicles enzyme compartmentalization liquid-liquid phase separation membranes protocells Peptides Polymers Tyrosine 42HK56048U mehr... RNA 63231-63-0
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520 |a Coacervates droplets have long been considered as potential protocells to mimic living cells. However, these droplets lack a membrane and are prone to coalescence, limiting their ability to survive, interact, and organize into higher-order assemblies. This work shows that tyrosine-rich peptide conjugates can undergo liquid-liquid phase separation in a well-defined pH window and transform into stable membrane-enclosed protocells by enzymatic oxidation and cross-linking at the liquid-liquid interface. The oxidation of the tyrosine-rich peptides into dityrosine creates a semipermeable, flexible membrane around the coacervates with tunable thickness, which displays strong intrinsic fluorescence, and stabilizes the coacervate protocells against coalescence. The membranes have an effective molecular weight cut-off of 2.5 kDa, as determined from the partitioning of small dyes and labeled peptides, RNA, and polymers into the membrane-enclosed coacervate protocells. Flicker spectroscopy reveals a membrane bending rigidity of only 0.1kB T, which is substantially lower than phospholipid bilayers despite a larger membrane thickness. Finally, it is shown that enzymes can be stably encapsulated inside the protocells and be supplied with substrates from outside, which opens the way for these membrane-bound compartments to be used as molecularly crowded artificial cells capable of communication or as a vehicle for drug delivery 
650 4 |a Journal Article 
650 4 |a coacervate-core vesicles 
650 4 |a enzyme compartmentalization 
650 4 |a liquid-liquid phase separation 
650 4 |a membranes 
650 4 |a protocells 
650 7 |a Peptides  |2 NLM 
650 7 |a Polymers  |2 NLM 
650 7 |a Tyrosine  |2 NLM 
650 7 |a 42HK56048U  |2 NLM 
650 7 |a RNA  |2 NLM 
650 7 |a 63231-63-0  |2 NLM 
700 1 |a Law, Jack O  |e verfasserin  |4 aut 
700 1 |a Grellscheid, Sushma N  |e verfasserin  |4 aut 
700 1 |a Huck, Wilhelm T S  |e verfasserin  |4 aut 
700 1 |a Spruijt, Evan  |e verfasserin  |4 aut 
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773 1 8 |g volume:34  |g year:2022  |g number:34  |g day:07  |g month:08  |g pages:e2202913 
856 4 0 |u http://dx.doi.org/10.1002/adma.202202913  |3 Volltext 
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