Thaler C D, Haimo L T
Department of Biology, University of California, Riverside, USA.
Int Rev Cytol. 1996;164:269-327. doi: 10.1016/s0074-7696(08)62388-8.
Microtubule-based motility is precisely regulated, and the targets of regulation may be the motor proteins, the microtubules, or both components of this intricately controlled system. Regulation of microtubule behavior can be mediated by cell cycle-dependent changes in centrosomal microtubule nucleating ability and by cell-specific, microtubule-associated proteins (MAPs). Changes in microtubule organization and dynamics have been correlated with changes in phosphorylation. Regulation of motor proteins may be required both to initiate movement and to dictate its direction. Axonemal and cytoplasmic dyneins as well as kinesin can be phosphorylated and this modification may affect the motor activities of these enzymes or their ability to interact with organelles. A more complete understanding of how motors can be modulated by phosphorylation, either of the motor proteins or of other associated substrates, will be necessary in order to understand how bidirectional transport is regulated.
基于微管的运动受到精确调控,调控的靶点可能是运动蛋白、微管,或者是这个复杂控制系统的两个组成部分。微管行为的调控可通过中心体微管成核能力的细胞周期依赖性变化以及细胞特异性的微管相关蛋白(MAPs)来介导。微管组织和动力学的变化与磷酸化的变化相关。运动蛋白的调控可能在启动运动和决定其方向两方面都有必要。轴丝动力蛋白和胞质动力蛋白以及驱动蛋白都可以被磷酸化,这种修饰可能会影响这些酶的运动活性或它们与细胞器相互作用的能力。为了理解双向运输是如何被调控的,有必要更全面地了解运动蛋白或其他相关底物的磷酸化如何调节运动蛋白。