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结合显微荧光测定法进行显微注射,以研究质子沿磷脂膜的扩散。

Microinjection in combination with microfluorimetry to study proton diffusion along phospholipid membranes.

作者信息

Antonenko Yuri N, Pohl Peter

机构信息

A.N. Belozersky Institute of Physico-Chemical Biology, Moscow State University, Moscow, 119992, Russia.

出版信息

Eur Biophys J. 2008 Jul;37(6):865-70. doi: 10.1007/s00249-008-0295-y. Epub 2008 Mar 11.

Abstract

Proton diffusion along the surface of a planar bilayer lipid membrane was measured by means of acid/base injection with a micropipette and recording of the kinetics of fluorescence changes of fluorescein-labelled lipid on the surface. The dimensionality of the process was assayed by fitting the kinetic curves with two-dimensional (2D) or three-dimensional (3D) diffusion equations. In agreement with Serowy et al. (Biophys J 84:1031-1037, 2003), lateral proton diffusion proceeded via bulk phase by means of buffer molecules as proton carriers (D = 600 microm2/s) under the conditions of 1 mM buffer in the solution. Introduction of proton binding sites on the membrane surface led to the appearance of a considerable contribution of two-dimensional proton diffusion on the membrane surface with D = 1,100 mum(2)/s. The system described can be used to study the dependence of the proton diffusion rate on the phospholipid and protein composition of the membrane.

摘要

通过用微量移液器进行酸/碱注入并记录表面上荧光素标记脂质的荧光变化动力学,来测量质子沿平面双层脂质膜表面的扩散。通过将动力学曲线与二维(2D)或三维(3D)扩散方程拟合来测定该过程的维度。与Serowy等人(《生物物理杂志》84:1031 - 1037,2003年)的研究一致,在溶液中1 mM缓冲液的条件下,横向质子扩散通过缓冲分子作为质子载体在体相当中进行(D = 600平方微米/秒)。在膜表面引入质子结合位点导致二维质子在膜表面扩散的显著贡献出现,其扩散系数D = 1100平方微米/秒。所描述的系统可用于研究质子扩散速率对膜的磷脂和蛋白质组成的依赖性。

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