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踝蛋白-肌动蛋白结合的动力学测定

Kinetic determination of talin-actin binding.

作者信息

Goldmann W H, Isenberg G

机构信息

Dept. of Biophysics, Technical University of Munich, Garching, FRG.

出版信息

Biochem Biophys Res Commun. 1991 Jul 31;178(2):718-23. doi: 10.1016/0006-291x(91)90167-6.

Abstract

Smooth muscle talin prepared from chicken gizzard binds to skeletal muscle actin in vitro. The stoichiometry of 1:3 for talin:fluorescent labelled G-actin was confirmed by steady state titration and viscosity measurements under non-polymerizing conditions. The binding constant (Kd) of talin and G-actin was determined by continuous fluorescence titration and gave a value of approx 0.3 microM. The association rate constant of talin and fluorescent labelled G-actin of approx 7 x 10(6) M-1 x s-1 was ascertained by the stopped flow method; the dissociation rate constant was calculated at approx 2-3 s-1.

摘要

从鸡肫制备的平滑肌踝蛋白在体外可与骨骼肌肌动蛋白结合。在非聚合条件下,通过稳态滴定和粘度测量确定了踝蛋白与荧光标记的球形肌动蛋白的化学计量比为1:3。通过连续荧光滴定测定踝蛋白与球形肌动蛋白的结合常数(Kd),其值约为0.3微摩尔。采用停流法确定踝蛋白与荧光标记的球形肌动蛋白的缔合速率常数约为7×10⁶ M⁻¹·s⁻¹;解离速率常数经计算约为2 - 3 s⁻¹。

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