Centre for Mechanochemical Cell Biology, Warwick Medical School, University of Warwick, Coventry, CV4 7AL, United Kingdom.
Semin Cell Dev Biol. 2011 Dec;22(9):927-34. doi: 10.1016/j.semcdb.2011.09.021. Epub 2011 Oct 5.
The simple mechanistic and functional division of the kinesin family into either active translocators or non-motile microtubule depolymerases was initially appropriate but is now proving increasingly unhelpful, given evidence that several translocase kinesins can affect microtubule dynamics, whilst non-translocase kinesins can promote microtubule assembly and depolymerisation. Such multi-role kinesins act either directly on microtubule dynamics, by interaction with microtubules and tubulin, or indirectly, through the transport of other factors along the lattice to the microtubule tip. Here I review recent progress on the mechanisms and roles of these translocase kinesins.
最初,将驱动蛋白家族简单地划分为活性转运蛋白或非运动微管解聚酶的机械和功能分类是合理的,但现在越来越没有帮助,因为有证据表明,一些转运蛋白驱动蛋白可以影响微管动力学,而非转运蛋白驱动蛋白可以促进微管组装和解聚。这些多功能驱动蛋白通过与微管和微管蛋白相互作用直接作用于微管动力学,或者通过将其他因子沿着晶格运输到微管末端来间接作用。在这里,我回顾了这些转运蛋白驱动蛋白的机制和作用的最新进展。