Howard T H, Lin S
J Supramol Struct. 1979;11(3):283-93. doi: 10.1002/jss.400110303.
The cytochalasins (CE, CD, CB and H2CB) inhibit numerous cellular processes which require the interaction of actin with other structural and contractile proteins. In this report we describe the effects of the cytochalasins on the viscosity and morphology of muscle and platelet actin. The cytochalasins decreased the viscosity of F-actin solutions. The effect of H2CB, CB and CD ON F-actin viscosity was maximal at concentrations of 20-50 micro M and did not increase with time. In contrast, CE caused a progressive decrease in the viscosity of F-actin solutions which was dependent upon the concentration of CE and the duration of incubation of the CE-actin mixture. After two hours of incubation of drug-actin mixtures, the relative effectiveness of the cytochalasins in reducing the viscosity of F-actin was CE greater than CD greater than CB=H2CB. The effects of CD and CE were paralleled by morphologic changes in negatively stained actin filaments. The effects of the cytochalasins on the viscosity and morphology of muscle and platelet actin were the same whether the drugs were added before or after the polymerization of the protein. These studies show that the interaction of the cytochalasins with actin is highly specific. Because the relative potencies of these drugs for affecting motile processes and the relative affinities of the drugs for binding sites within a variety of cells are CE greater than CD greater than CB=H2CB, the effects of cytochalasins on actin described here may contribute to some of the biological effects of the drugs on motile processes.
细胞松弛素(CE、CD、CB和H2CB)抑制许多需要肌动蛋白与其他结构蛋白和收缩蛋白相互作用的细胞过程。在本报告中,我们描述了细胞松弛素对肌肉和血小板肌动蛋白的粘度和形态的影响。细胞松弛素降低了F-肌动蛋白溶液的粘度。H2CB、CB和CD对F-肌动蛋白粘度的影响在浓度为20 - 50微摩尔时最大,且不随时间增加。相比之下,CE导致F-肌动蛋白溶液的粘度逐渐降低,这取决于CE的浓度和CE-肌动蛋白混合物的孵育时间。药物-肌动蛋白混合物孵育两小时后,细胞松弛素在降低F-肌动蛋白粘度方面的相对效力为CE大于CD大于CB = H2CB。CD和CE的作用伴随着负染肌动蛋白丝的形态变化。无论药物是在蛋白质聚合之前还是之后添加,细胞松弛素对肌肉和血小板肌动蛋白的粘度和形态的影响都是相同的。这些研究表明,细胞松弛素与肌动蛋白的相互作用具有高度特异性。由于这些药物影响运动过程的相对效力以及它们对多种细胞内结合位点的相对亲和力为CE大于CD大于CB = H2CB,本文所述的细胞松弛素对肌动蛋白的影响可能有助于解释这些药物对运动过程的一些生物学效应。