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与兔骨骼肌F-肌动蛋白和疟原虫肌动蛋白聚合物共轭的N-(3-芘基)马来酰亚胺的荧光研究。

Fluorescence study of N-(3-pyrene)maleimide conjugated to rabbit skeletal F-actin and plasmodium actin polymers.

作者信息

Kawasaki Y, Mihashi K, Tanaka H, Ohnuma H

出版信息

Biochim Biophys Acta. 1976 Sep 28;446(1):166-78. doi: 10.1016/0005-2795(76)90108-2.

Abstract

A fluorescent probe N-(3-pyrene)maleimide was conjugated to rabbit skeletal F-actin at the site of most reactive sulfhydryl group (Cys-373). Its fluorescence anisotropy decay showed a single correlation time of 560 ns at 25 degrees C, which is in a very good agreement with the correlation time of the dansyl-L-cysteine group conjugated to the same site of F-actin reported very recently [Wahl, Ph., Mihashi, K, and Auchet, J-C. (1975) FEBS Lett. 8, 164-167]. Actin from plasmodia of myxomycates, Physarum polycepharum, was also conjugated with N-(3-pyrene) maleimide and the fluorescence anisotropy was compared with rabbit skeletal F-actin using the classical steady excitation method. It was found that the internal mobility of the magnesium polymer of plasmodium actin is remarkably larger than both plasmodium F-actin and rabbit skeletal F-actin.

摘要

一种荧光探针N-(3-芘基)马来酰亚胺在最具反应活性的巯基(半胱氨酸-373)位点与兔骨骼肌F-肌动蛋白结合。其荧光各向异性衰减在25℃时显示出单一的相关时间为560纳秒,这与最近报道的与F-肌动蛋白相同位点结合的丹磺酰-L-半胱氨酸基团的相关时间非常吻合[瓦尔,Ph.,三桥,K,和奥谢,J-C.(1975年)《欧洲生物化学学会联合会快报》8,164 - 167]。黏菌多头绒泡菌的原质团中的肌动蛋白也与N-(3-芘基)马来酰亚胺结合,并使用经典的稳态激发方法将其荧光各向异性与兔骨骼肌F-肌动蛋白进行比较。发现原质团肌动蛋白的镁聚合物的内部流动性明显大于原质团F-肌动蛋白和兔骨骼肌F-肌动蛋白。

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