Assembly of photosynthetic reaction center with ABA tri-block polymersomes: highlights on the protein localization.
AuthorsTangorra, Roberto Rocco
Hassan Omar, Omar
De Leo, Vincenzo
KAUST DepartmentBiological and Environmental Sciences and Engineering (BESE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/559597
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AbstractThe reconstitution of the integral membrane protein photosynthetic reaction center (RC) in polymersomes, i. e. artificial closed vesicles, was achieved by the micelle-to-vesicle transition technique, a very mild protocol based on size exclusion chromatography often used to drive the incorporation of proteins contemporarily to liposomes formation. An optimized protocol was used to successfully reconstitute the protein in a fully active state in polymersomes formed by the tri-block copolymers PMOXA22-PDMS61-PMOXA22. The RC is very sensitive to its solubilizing environment and was used to probe the positioning of the protein in the vesicles. According to charge-recombination experiments and to the enzymatic activity assay, the RC is found to accommodate in the PMOXA22 region of the polymersome, facing the water bulk solution, rather than in the PDMS61 transmembrane-like region. Furthermore, polymersomes were found to preserve protein integrity efficiently as the biomimetic lipid bilayers but show a much longer temporal stability than lipid based vesicles.
CitationAssembly of photosynthetic reaction center with ABA tri-block polymersomes: highlights on the protein localization. 2015 Photochem. Photobiol. Sci.
PublisherRoyal Society of Chemistry (RSC)
JournalPhotochem. Photobiol. Sci.