Simon J R, Parsons S F, Salmon E D
Department of Biology, University of North Carolina, Chapel Hill 27599-7260.
Cell Motil Cytoskeleton. 1992;21(1):1-14. doi: 10.1002/cm.970210102.
The dynamic instability of individual microtubules (Mts) in cytoplasmic extracts or assembled from highly purified sea urchin egg tubulin was examined using video-enhanced, differential-interference contrast (VE-DIC) light microscopy. Extract Mts (endogenous tubulin = 12.1 microM) displayed only plus-ended growth. The elongation velocity was 7.8 microns/min for an average duration of 1.3 min before switching (catastrophe) to rapid shortening, which occurred at 13.0 microns/min for an average duration of 0.5 min before switching (rescue) back to the elongation phase. These parameters are typical of interphase Mt dynamic instability. Surprisingly, Mts assembled from purified urchin egg tubulin in standard buffers were less dynamic that those reported for purified brain tubulin or Mts in the extract. Buffer parameters were changed in an attempt to mimic the extract Mt results. The pH buffer itself, Hepes or Pipes, drastically altered Mt dynamics but could not achieve high elongation velocity with high catastrophe frequencies. Calcium at 1 microM had negligible effects, while increasing pH from 6.9 to 7.2 stimulated elongation velocity. Finally, Mt dynamics of purified egg tubulin (11.9 microM) were assayed in ultrafiltrates (MW cut-off less than 30 kD) of the cytoplasmic extracts. Mts elongated slowly at 1.2 microns/min for 26 min before a catastrophe and rapid shortening at 11.8 microns/min. Rescue was less frequent than unfiltered extracts, minus-ended growth was observed, and self-assembly occurred at slightly higher tubulin concentrations. Therefore, the egg extracts and cytoplasm must contain non-buffer factors which stimulate elongation velocity by 6.5-fold without self-assembly, increase catastrophe frequency by 20-fold, and block minus-ended growth.
利用视频增强型微分干涉相差(VE-DIC)光学显微镜,研究了细胞质提取物中或由高度纯化的海胆卵微管蛋白组装而成的单个微管(Mts)的动态不稳定性。提取物微管(内源性微管蛋白=12.1微摩尔)仅表现出正端生长。伸长速度为7.8微米/分钟,平均持续1.3分钟,然后转换(灾变)为快速缩短,快速缩短速度为13.0微米/分钟,平均持续0.5分钟,之后再转换(拯救)回到伸长阶段。这些参数是间期微管动态不稳定性的典型特征。令人惊讶的是,在标准缓冲液中由纯化的海胆卵微管蛋白组装而成的微管,其动态性比纯化的脑微管蛋白或提取物中的微管报道的要低。尝试改变缓冲液参数以模拟提取物微管的结果。缓冲液本身,即Hepes或Pipes,会极大地改变微管动态性,但无法在高灾变频率下实现高伸长速度。1微摩尔的钙影响可忽略不计,而将pH从6.9提高到7.2会刺激伸长速度。最后,在细胞质提取物的超滤物(截留分子量小于30 kD)中测定了纯化的卵微管蛋白(11.9微摩尔)的微管动态性。微管在灾变前以1.2微米/分钟的速度缓慢伸长26分钟,然后以11.8微米/分钟的速度快速缩短。拯救比未过滤的提取物更不频繁,观察到了负端生长,并且在略高的微管蛋白浓度下发生了自组装。因此,卵提取物和细胞质中必定含有非缓冲因子,这些因子可将伸长速度提高6.5倍而不发生自组装,将灾变频率提高20倍,并阻止负端生长。