Saito S, Watabe S, Ozaki H, Kigoshi H, Yamada K, Fusetani N, Karaki H
Department of Veterinary Pharmacology, Graduate School of Agriculture and Life Sciences, University of Tokyo.
J Biochem. 1996 Sep;120(3):552-5. doi: 10.1093/oxfordjournals.jbchem.a021449.
Aplyronine A is a macrolide isolated from Aplysia kurodai. By monitoring fluorescent intensity of pyrenyl-actin, it was found that aplyronine A inhibited both the velocity and the degree of actin polymerization. Aplyronine A also quickly depolymerized F-actin. The kinetics of depolymerization suggest that aplyronine A severs F-actin. The relationship between the concentration of total actin and F-actin at different concentrations of aplyronine A suggests that aplyronine A forms a 1:1 complex with G-actin. From these results, it is concluded that aplyronine A inhibits actin polymerization and depolymerizes F-actin by nibbling. Comparison of the chemical structure of aplyronine A and another actin-depolymerizing macrolide, mycalolide B, suggests that the side-chain but not the macrolide ring of aplyronine A may account for its actin binding and severing activity.
阿普利罗宁A是一种从黑指纹海兔中分离出的大环内酯。通过监测芘基肌动蛋白的荧光强度,发现阿普利罗宁A既抑制肌动蛋白聚合的速度,也抑制其聚合程度。阿普利罗宁A还能使F-肌动蛋白迅速解聚。解聚动力学表明阿普利罗宁A切断F-肌动蛋白。在不同浓度的阿普利罗宁A下,总肌动蛋白和F-肌动蛋白浓度之间的关系表明,阿普利罗宁A与G-肌动蛋白形成1:1复合物。从这些结果可以得出结论,阿普利罗宁A通过蚕食抑制肌动蛋白聚合并使F-肌动蛋白解聚。对阿普利罗宁A和另一种肌动蛋白解聚大环内酯——麦考酚酸B的化学结构比较表明,阿普利罗宁A的侧链而非大环内酯环可能是其肌动蛋白结合和切断活性的原因。