Wolff J, Knipling L, Cahnmann H J, Palumbo G
National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2820-4. doi: 10.1073/pnas.88.7.2820.
Ultraviolet irradiation of the [3H]colchicine-tubulin complex leads to direct photolabeling of tubulin with low but practicable efficiency. The bulk (70% to greater than 90%) of the labeling occurs on beta-tubulin and appears early after irradiation, whereas alpha-tubulin is labeled later. The labeling ratio of beta-tubulin to alpha-tubulin (beta/alpha ratio) is reduced by prolonged incubation, prolonged irradiation, urea, high ionic strength, the use of aged tubulin, dilution of tubulin, or large concentrations of colchicine or podophyllotoxin. Glycerol increases the beta/alpha ratio. Limited data with [3H]podophyllotoxin show that it covalently bound with a similar beta/alpha distribution. Vinblastine, on the other hand, exhibits preferential attachment to alpha-tubulin. The possibilities that colchicine binds at the interface between alpha-tubulin and beta-tubulin, that the drug spans this interface, and that both subunits may contribute to the binding site are suggested.
用[3H]秋水仙碱 - 微管蛋白复合物进行紫外线照射,可导致微管蛋白的直接光标记,效率虽低但切实可行。大部分(70%至大于90%)标记发生在β - 微管蛋白上,且在照射后早期出现,而α - 微管蛋白的标记较晚。β - 微管蛋白与α - 微管蛋白的标记比率(β/α比率)会因长时间孵育、长时间照射、尿素、高离子强度、使用老化的微管蛋白、微管蛋白稀释或高浓度秋水仙碱或鬼臼毒素而降低。甘油会增加β/α比率。关于[3H]鬼臼毒素的有限数据表明,它以类似的β/α分布共价结合。另一方面,长春花碱表现出对α - 微管蛋白的优先附着。由此推测秋水仙碱可能在α - 微管蛋白和β - 微管蛋白的界面处结合,药物跨越该界面,且两个亚基都可能对结合位点有贡献。