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Molecular Design of Chemically Fueled Peptide–Polyelectrolyte Coacervate-Based Assemblies

Complex coacervated-based assemblies form when two oppositely charged polyelectrolytes combine to phase separate into a supramolecular architecture. These architectures range from complex coacervate droplets, spherical and worm-like micelles, to vesicles. These assemblies are widely applied, for exa...

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Published in:Journal of the American Chemical Society 2021-03, Vol.143 (12), p.4782-4789
Main Authors: Späth, Fabian, Donau, Carsten, Bergmann, Alexander M, Kränzlein, Moritz, Synatschke, Christopher V, Rieger, Bernhard, Boekhoven, Job
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Language:English
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cited_by cdi_FETCH-LOGICAL-a324t-7b01971ccce794bf170364503f4126dcd8295631de071f3db0d5a6553bb3530b3
cites cdi_FETCH-LOGICAL-a324t-7b01971ccce794bf170364503f4126dcd8295631de071f3db0d5a6553bb3530b3
container_end_page 4789
container_issue 12
container_start_page 4782
container_title Journal of the American Chemical Society
container_volume 143
creator Späth, Fabian
Donau, Carsten
Bergmann, Alexander M
Kränzlein, Moritz
Synatschke, Christopher V
Rieger, Bernhard
Boekhoven, Job
description Complex coacervated-based assemblies form when two oppositely charged polyelectrolytes combine to phase separate into a supramolecular architecture. These architectures range from complex coacervate droplets, spherical and worm-like micelles, to vesicles. These assemblies are widely applied, for example, in the food industry, and as underwater or medical adhesives, but they can also serve as a great model for biological assemblies. Indeed, biology relies on complex coacervation to form so-called membraneless organelles, dynamic and transient droplets formed by the coacervation of nucleic acids and proteins. To regulate their function, membraneless organelles are dynamically maintained by chemical reaction cycles, including phosphorylation and dephosphorylation, but exact mechanisms remain elusive. Recently, some model systems also regulated by chemical reaction cycles have been introduced, but how to design such systems and how molecular design affects their properties is unclear. In this work, we test a series of cationic peptides for their chemically fueled coacervation, and we test how their design can affect the dynamics of assembly and disassembly of the emerging structures. We combine them with both homo- and block copolymers and study the morphologies of the assemblies, including morphological transitions that are driven by the chemical reaction cycle. We deduce heuristic design rules that can be applied to other chemically regulated systems. These rules will help develop membraneless organelle model systems and lead to exciting new applications of complex coacervate-based examples like temporary adhesives.
doi_str_mv 10.1021/jacs.1c01148
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title Molecular Design of Chemically Fueled Peptide–Polyelectrolyte Coacervate-Based Assemblies
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