Oda Toshiro, Crane Zackary D, Dicus Christopher W, Sufi Bilal A, Bates Robert B
Department of Biophysics, Max Planck Institute for Medical Research, Jahnstr 29, Heidelberg, D-69120, Germany.
J Mol Biol. 2003 Apr 25;328(2):319-24. doi: 10.1016/s0022-2836(03)00306-1.
Dolastatin 11, a drug isolated from the Indian Ocean sea hare Dolabella auricularia, arrests cytokinesis in vivo and increases the amount of F-actin to stabilize F-actin in vitro, like phalloidin and jasplakinolide. However, according to the previous biochemical study, the binding of dolastatin 11 to F-actin does not compete with that of phalloidin, suggesting that the binding sites are different. To understand the mechanism of F-actin stabilization by dolastatin 11, we determined the position of bound dolastatin 11 in F-actin using the X-ray fiber diffraction from oriented filament sols. Our analysis shows that the position of dolastatin 11 is clearly different from that of phalloidin. However, these bound drugs are present in the gap between the two long-pitch F-actin strands in a similar way. The result suggests that the connection between the two long-pitch F-actin strands might be a key for the control of F-actin stabilization.
多拉司他汀11是一种从印度洋海兔耳状多肋鳃海蛞蝓中分离出的药物,它能在体内阻止胞质分裂,并在体外增加F-肌动蛋白的量以稳定F-肌动蛋白,类似于鬼笔环肽和茉莉酮酸酯。然而,根据之前的生化研究,多拉司他汀11与F-肌动蛋白的结合并不与鬼笔环肽竞争,这表明结合位点不同。为了了解多拉司他汀11稳定F-肌动蛋白的机制,我们利用定向丝状溶胶的X射线纤维衍射确定了多拉司他汀11在F-肌动蛋白中的结合位置。我们的分析表明,多拉司他汀11的位置与鬼笔环肽明显不同。然而,这些结合的药物以类似的方式存在于两条长间距F-肌动蛋白链之间的间隙中。结果表明,两条长间距F-肌动蛋白链之间的连接可能是控制F-肌动蛋白稳定性的关键。