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鲑精蛋白AI的荧光探针研究

A fluorescent probe study of salmine AI.

作者信息

Russo S F, Engel R G

出版信息

Physiol Chem Phys. 1978;10(2):163-76.

PMID:569339
Abstract

A fluorescent probe, 1-p-toluidinylnapthalene-8-sulfonate (1,8-TNS), was used to study the nonpolar sites on salmine AI. Fluorescence enhancement resulting from binding between the probe and the protein occurs at a wavelength of maximum emission of 497-500 nm, indicating the existence of moderately nonpolar binding sites on salmine AI. Fluorescence enhancement decreases as the ionic strength of the solvent is increased from 0.002 M to 0.050 M. Fluorescence increases with increasing acidity although this effect is not correlated to the pKa of 1,8-TNS. Positive cooperative binding takes place between 1,8-TNS and salmine AI. Equilibrium dialysis indicates that binding occurs only under conditions resulting in significant fluorescent enhancement. The binding was also studied using thin film dialysis, which is much faster than equilibrium dialysis and avoids the observed changes in probe-protein interaction that occur over long time periods with the latter system.

摘要

一种荧光探针,1-对甲苯胺基萘-8-磺酸盐(1,8-TNS),被用于研究鲑精蛋白AI上的非极性位点。探针与蛋白质结合导致的荧光增强发生在最大发射波长497 - 500 nm处,表明鲑精蛋白AI上存在适度非极性结合位点。当溶剂的离子强度从0.002 M增加到0.050 M时,荧光增强减弱。荧光随酸度增加而增强,尽管这种效应与1,8-TNS的pKa无关。1,8-TNS与鲑精蛋白AI之间发生正协同结合。平衡透析表明,结合仅在导致显著荧光增强的条件下发生。还使用薄膜透析研究了结合情况,薄膜透析比平衡透析快得多,并且避免了在长时间使用后一种系统时观察到的探针 - 蛋白质相互作用的变化。

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