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• W1982727647 abstract "We have developed a facile, scalable method for preparation of enzyme-responsive copolypeptide vesicles that requires no protecting groups or expensive components. We designed amphiphilic copolypeptides containing segments of water-soluble methionine sulfoxide, M(O), residues that were prepared by synthesis of a fully hydrophobic precursor diblock copolypeptide, poly(l-methionine)65-b-poly(L-leucine0.5-stat-L-phenylalanine0.5)20, M65(L0.5/F0.5)20, followed by its direct oxidation in water to give the amphiphilic M(O) derivative, M(O)65(L0.5/F0.5)20. Assembly of M(O)65(L0.5/F0.5)20 in water gave vesicles with average diameters of a few micrometers that could then be extruded to nanoscale diameters. The M(O) segments in the vesicles were found to be substrates for reductase enzymes, which regenerated hydrophobic M segments and resulted in a change in supramolecular morphology that caused vesicle disruption and release of cargos." @default.
• W1982727647 created "2016-06-24" @default.
• W1982727647 creator A5020764051 @default.
• W1982727647 creator A5032184271 @default.
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• W1982727647 date "2013-09-09" @default.
• W1982727647 modified "2023-10-08" @default.
• W1982727647 title "Enzyme-Triggered Cargo Release from Methionine Sulfoxide Containing Copolypeptide Vesicles" @default.
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• W1982727647 doi "https://doi.org/10.1021/bm400971p" @default.
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