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Issue title: 25th Anniversary Volume. Dedicated in Memory and in Honor of George William Scott Blair. 23 July 1902 to 30 September 1987
Article type: Research Article
Authors: Kinjo, M. | Araiso, T. | Koyama, T.
Affiliations: Section of Physiology, Research Institute of Applied Electricity, Hokkaido University, Sapporo, 060, Japan
Note: [] Accepted by: Editor E. Fukada
Abstract: Membrane fluidity and osmotic sensitivity were examined in DPPC liposomes treated with phospholipase A2 (PL.A2) in the presence of Ca2+ or Mg2+. The amount of liposome phospholipid hydrolyzed differed with the two ions. Embedded DPH, a rod-like fluorescent probe, was employed in the determination of membrane fluidity. Membrane fluidity decreased according to the degree of phospholipid hydrolization in liposomes by PL.A2. The reciprocal value of absorption at 450 nm was measured as the index of osmotic sensitivity of liposomes. Intact sonicated liposomes showed osmotic insensitivity. PL.A2-treated liposomes in which about 40 % of total phospholipid was hydrolyzed showed osmotic sensitivity. No change in the membrane fluidity was obtained when PL.A2-treated liposomes were exposed to hypertonic or hypotonic solution. These results suggested that the motion of the acyl-chain of phospholipids and free fatty acids was resisted in PL.A2-treated liposomes. The resistance may be due to a phase separation between phospholipids and free fatty acids. The pore for water permeation might be induced in the border between phase-separated domains in PL.A2-treated liposomes.
Keywords: 1,6-diphenyl-1,3,5-hexatriene, fluorescence anisotropy, liposome, permeability, phospholipase A2, membrane fluidity
DOI: 10.3233/BIR-1988-25311
Journal: Biorheology, vol. 25, no. 3, pp. 517-525, 1988
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