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Aqueous photo-RAFT polymerization under ambient conditions: synthesis of protein-polymer hybrids in open air.

Authors :
Jazani AM
Murata H
Cvek M
Lewandowska-Andralojc A
Bernat R
Kapil K
Hu X
De Luca Bossa F
Szczepaniak G
Matyjaszewski K
Source :
Chemical science [Chem Sci] 2024 May 24; Vol. 15 (25), pp. 9742-9755. Date of Electronic Publication: 2024 May 24 (Print Publication: 2024).
Publication Year :
2024

Abstract

A photoinduced reversible addition-fragmentation chain-transfer (photo-RAFT) polymerization technique in the presence of sodium pyruvate (SP) and pyruvic acid derivatives was developed. Depending on the wavelength of light used, SP acted as a biocompatible photoinitiator or promoter for polymerization, allowing rapid open-to-air polymerization in aqueous media. Under UV irradiation (370 nm), SP decomposes to generate CO <subscript>2</subscript> and radicals, initiating polymerization. Under blue (450 nm) or green (525 nm) irradiation, SP enhances the polymerization rate via interaction with the excited state RAFT agent. This method enabled the polymerization of a range of hydrophilic monomers in reaction volumes up to 250 mL, eliminating the need to remove radical inhibitors from the monomers. In addition, photo-RAFT polymerization using SP allowed for the facile synthesis of protein-polymer hybrids in short reaction times (<1 h), low organic content (≤16%), and without rigorous deoxygenation and the use of transition metal photocatalysts. Enzymatic studies of a model protein (chymotrypsin) showed that despite a significant loss of protein activity after conjugation with RAFT chain transfer agents, the grafting polymers from proteins resulted in a 3-4-fold recovery of protein activity.<br />Competing Interests: The authors declare no competing financial interest.<br /> (This journal is © The Royal Society of Chemistry.)

Details

Language :
English
ISSN :
2041-6520
Volume :
15
Issue :
25
Database :
MEDLINE
Journal :
Chemical science
Publication Type :
Academic Journal
Accession number :
38939137
Full Text :
https://doi.org/10.1039/d4sc01409j