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• W4387310523 abstract "Protocells have garnered considerable attention from cell biologists, materials scientists, and synthetic biologists. Phase-separating coacervate microdroplets have emerged as a promising cytomimetic model because they can internalize and concentrate components from dilute surrounding environments. However, the membrane-free nature of such coacervates leads to coalescence into a bulk phase, a phenomenon that is not representative of the cells they are designed to mimic. Herein, we develop a membranized peptide coacervate (PC) with oppositely charged oligopeptides as the molecularly crowded cytosol and a metal–phenolic network (MPN) coating as the membrane. The hybrid protocell efficiently internalizes various bioactive macromolecules (e.g., bovine serum albumin and immunoglobulin G) (>90%) while also resisting radicals due to the semipermeable cytoprotective membrane. Notably, the resultant PC@MPNs are capable of anabolic cascade reactions and remain in discrete protocellular populations without coalescence. Finally, we demonstrate that the MPN protocell membrane can be postfunctionalized with various functional molecules (e.g., folic acid and fluorescence dye) to more closely resemble actual cells with complex membranes, such as recognition molecules, which allows for drug delivery. This membrane-bound cytosolic protocell structure paves the way for innovative synthetic cells with structural and functional complexity." @default.
• W4387310523 created "2023-10-04" @default.
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• W4387310523 date "2023-10-03" @default.
• W4387310523 modified "2023-10-15" @default.
• W4387310523 title "Peptide-Based Coacervate Protocells with Cytoprotective Metal–Phenolic Network Membranes" @default.
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• W4387310523 doi "https://doi.org/10.1021/jacs.3c07748" @default.
• W4387310523 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37788442" @default.
• W4387310523 hasPublicationYear "2023" @default.
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