Caplow M, Langford G M, Zeeberg B
J Biol Chem. 1982 Dec 25;257(24):15012-21.
Radioactive tubulin subunit incorporation into porcine and dogfish shark brain microtubules which are at steady state has been found to result primarily from a diffusional reaction, in which subunits are incorporated although there are an equal number of tubulin subunit additions to and losses from each of the two microtubule ends in a unit of time. Treadmilling is very inefficient, and the Wegner s-values are equal to 0.0005-0.001. At steady state there are approximately 5000 (pig brain) or 2500 (dogfish brain) tubulin subunits lost from the two microtubule ends/s; an equivalent number of subunit addition reactions maintains a constant microtubule mass. The rate constants for subunit loss and addition with porcine brain microtubules, determined from analysis of the steady state rate for radioactive subunit incorporation, are much larger than those measured previously, when the rate constants were determined from the disassembly rate following perturbation of the steady state by dilution (Zeeberg, B., Reid, R., and Caplow, M. (1980) J. Biol. Chem. 255, 9891-9899). To account for this discrepancy it is suggested that at steady state the microtubule is capped by a short finite length of tubulin-GTP subunits, which undergo extremely facile association and dissociation (2500-5000 subunits/microtubule/s). This cap would be rapidly lost following dilution so that the observed rate only measures the relatively slow loss of tubulin-GDP subunits (120 subunits/microtubule/s) which had been in the interior of the microtubule; this is not equal to the rate constant for subunit loss (and addition) from the ends at steady state. Because of this, previous estimates of the Wegner s-value for treadmilling which utilized dilution for determining the steady state molecular rate constants for subunit loss are believed to be too high.
已发现,处于稳态的猪脑和姥鲨脑微管中,放射性微管蛋白亚基的掺入主要源于扩散反应。在该反应中,尽管在单位时间内两个微管末端的微管蛋白亚基添加数量与丢失数量相等,但亚基仍会掺入。踏车行为效率极低,韦格纳s值为0.0005 - 0.001。在稳态下,每秒约有5000个(猪脑)或2500个(姥鲨脑)微管蛋白亚基从两个微管末端丢失;同等数量的亚基添加反应维持了微管质量的恒定。通过分析放射性亚基掺入的稳态速率确定的猪脑微管亚基丢失和添加的速率常数,比之前通过稀释扰动稳态后从解聚速率测定的速率常数大得多(泽伯格、里德、卡普洛,1980年,《生物化学杂志》255卷,9891 - 9899页)。为了解释这种差异,有人提出在稳态下,微管由一段短的有限长度的微管蛋白 - GTP亚基封端,这些亚基经历极其容易的缔合和解离(每个微管每秒2500 - 5000个亚基)。稀释后,这个封端会迅速丢失,因此观察到的速率仅测量了原本在微管内部的微管蛋白 - GDP亚基相对较慢的丢失速率(每个微管每秒120个亚基);这与稳态下末端亚基丢失(和添加)的速率常数不相等。正因为如此,之前利用稀释法确定亚基丢失稳态分子速率常数来估算踏车行为韦格纳s值的结果被认为过高。