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关于在有氧条件下使用芘发光测量生物膜微粘度。

On measuring biomembrane microviscosity using pyrene luminescence in aerobic conditions.

作者信息

Vekshin N L

机构信息

Institute of Biological Physics, Acad. Sci. U.S.S.R., Pushchino, Moscow Region.

出版信息

J Biochem Biophys Methods. 1987 Nov;15(2):97-104. doi: 10.1016/0165-022x(87)90037-6.

Abstract

The movement of pyrene in a lipid bilayer is shown to occur not only in the lateral but also transmembrane direction. Within the excited state lifetime, the pyrene monomer elevates from the depth to the polar region of the membrane and emits a luminescence photon. The excimer does not exhibit any marked transmembrane movement. The luminescence quenching efficiency of monomers and excimers depends on the depth of penetration of the quencher into the membrane. In the lipid bilayer, pyrene luminescence is strongly quenched by oxygen. The binding of pyrene to membrane proteins protects it from quenching. It has been concluded that the widely used estimations of membrane viscosity from pyrene luminescence intensity are incorrect.

摘要

芘在脂质双层中的移动不仅发生在横向,也发生在跨膜方向。在激发态寿命内,芘单体从膜的深处提升至极性区域并发射一个发光光子。而准分子则未表现出任何显著的跨膜移动。单体和准分子的发光猝灭效率取决于猝灭剂进入膜内的深度。在脂质双层中,芘的发光会被氧气强烈猝灭。芘与膜蛋白的结合可保护其不被猝灭。得出的结论是,基于芘发光强度对膜粘度进行的广泛估计是不正确的。

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