Jordan M A, Wilson L
Department of Biological Sciences, University of California, Santa Barbara 93106.
Biochemistry. 1990 Mar 20;29(11):2730-9. doi: 10.1021/bi00463a016.
We have investigated the effects of vinblastine at micromolar concentrations and below on the dynamics of tubulin exchange at the ends of microtubule-associated-protein-rich bovine brain microtubules. The predominant behavior of these microtubules at polymer-mass steady state under the conditions examined was tubulin flux, i.e., net addition of tubulin at one end of each microtubule, operationally defined as the assembly or A end, and balanced net loss at the opposite (disassembly or D) end. No dynamic instability behavior could be detected by video-enhanced dark-field microscopy. Addition of vinblastine to the microtubules at polymer-mass steady state resulted in an initial concentration-dependent depolymerization predominantly at the A ends, until a new steady-state plateau at an elevated critical concentration was established. Microtubules ultimately attained the same stable polymer-mass plateau when vinblastine was added prior to initiation of polymerization as when the drug was added to already polymerized microtubules. Vinblastine inhibited tubulin exchange at the ends of the microtubules at polymer-mass steady state, as determined by using microtubules differentially radiolabeled at their opposite ends. Inhibition of tubulin exchange occurred at concentrations of vinblastine that had very little effect on polymer mass. Both the initial burst of incorporation that occurs in control microtubule suspensions following a pulse of labeled GTP and the relatively slower linear incorporation of label that follows the initial burst were inhibited in a concentration-dependent manner by vinblastine. Both processes were inhibited to the same extent at all vinblastine concentrations examined. If the initial burst of label incorporation represents a low degree of dynamic instability (very short excursions of growth and shortening of the microtubules at one or both ends), then vinblastine inhibits both dynamic instability and flux to similar extents. The ability of vinblastine to inhibit tubulin exchange at microtubule ends in the micromolar concentration range appeared to be mediated by the reversible binding of vinblastine to tubulin binding sites exposed at the polymer ends. Determination by dilution analysis of the effects of vinblastine on the apparent dissociation rate constants for tubulin loss at opposite microtubule ends indicated that a principal effect of vinblastine is to decrease the dissociation rate constant at A ends (i.e., it produces a kinetic cap at A ends), whereas it has no effect on the D-end dissociation rate constant.
我们研究了微摩尔浓度及以下长春花碱对富含微管相关蛋白的牛脑微管末端微管蛋白交换动力学的影响。在所研究的条件下,这些微管在聚合物质量稳态时的主要行为是微管蛋白通量,即每个微管一端微管蛋白的净添加,在操作上定义为组装端或A端,而在相对的另一端(拆卸端或D端)则是平衡的净损失。通过视频增强暗场显微镜未检测到动态不稳定性行为。在聚合物质量稳态下向微管中添加长春花碱会导致初始的浓度依赖性解聚,主要发生在A端,直到在升高的临界浓度下建立新的稳态平台。当在聚合开始前添加长春花碱时,微管最终达到的稳定聚合物质量平台与将药物添加到已聚合的微管时相同。通过使用在相对末端进行不同放射性标记的微管确定,长春花碱在聚合物质量稳态下抑制微管末端的微管蛋白交换。在对聚合物质量影响很小的长春花碱浓度下就发生了微管蛋白交换的抑制。在标记的GTP脉冲后对照微管悬浮液中发生的初始掺入爆发以及初始爆发后相对较慢的线性标记掺入,均被长春花碱以浓度依赖性方式抑制。在所检查的所有长春花碱浓度下,这两个过程均被抑制到相同程度。如果初始的标记掺入爆发代表低度的动态不稳定性(微管一端或两端生长和缩短的非常短的波动),那么长春花碱对动态不稳定性和通量的抑制程度相似。长春花碱在微摩尔浓度范围内抑制微管末端微管蛋白交换的能力似乎是由长春花碱与聚合物末端暴露的微管蛋白结合位点的可逆结合介导的。通过稀释分析确定长春花碱对微管相对末端微管蛋白损失的表观解离速率常数的影响表明,长春花碱的主要作用是降低A端的解离速率常数(即,它在A端产生一个动力学帽),而对D端解离速率常数没有影响。