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LIPOSOME FUSION AND LIPID EXCHANGE ON ULTRAVIOLET IRRADIATION OF LIPOSOMES CONTAINING A PHOTOCHROMIC PHOSPHOLIPID
Author(s) -
Morgan C. G.,
Yianni Y. P.,
Sandhu S. S.,
Mitchell A. C.
Publication year - 1995
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/j.1751-1097.1995.tb05233.x
Subject(s) - liposome , chemistry , photochemistry , vesicle , flash photolysis , phospholipid , photochromism , phosphatidylcholine , chromatography , membrane , kinetics , biochemistry , reaction rate constant , physics , quantum mechanics
— A photochromic phospholipid, 1,2‐bis[4‐(4‐ n ‐butylphenylazo)phenylbutyroyl]phosphatidyl‐choline (Bis‐Azo PC) has been incorporated into liposomes of gel‐ and liquid‐crystalline‐phase phospholipids. Liposomes of gel‐phase phospholipid are stable in the presence of the trans photostationary state Bis‐Az.o PC and can encapsulate fluorescent marker dye. On photoisomerization to the cis photostationary state, trapped marker is rapidly released. Liposomes containing Bis‐Azo PC can rapidly fuse together after UV isomerization, this process continuing in the dark. Exposure to white light causes reversion of Bis‐Azo PC to the trans form and halts dye leakage and vesicle fusion. Both unilamellar and multilamellar liposomes are able to fuse together on UV exposure. On UV photolysis, liposomes containing Bis‐Azo PC do not fuse with a large excess of unlabeled liposomes, but transfer of Bis‐Azo PC can be demonstrated spectrophotometrically. Vesicles of pure gel‐phase lipid containing trapped marker dye but initially no Bis‐Azo PC become leaky as a result of this lipid transfer. Liposomes composed of liquid‐crystalline‐phase phosphatidylcholine‐containing Bis‐Azo PC neither leak trapped marker nor fuse together on photolysis, nor do liquid‐crystalline‐phase liposomes fuse with gel‐phase liposomes under these conditions. These results are discussed together with some possible applications of liposome photodestabilization.