Department of Molecular and Cellular Biology, University of California, Davis, Davis, CA 95616, USA.
Department of Cell Biology and Human Anatomy, School of Medicine, University of California, Davis, Davis, CA 95616, USA.
Dev Cell. 2020 Apr 6;53(1):60-72.e4. doi: 10.1016/j.devcel.2020.01.029. Epub 2020 Feb 27.
Many eukaryotic cells distribute their intracellular components asymmetrically through regulated active transport driven by molecular motors along microtubule tracks. While intrinsic and extrinsic regulation of motor activity exists, what governs the overall distribution of activated motor-cargo complexes within cells remains unclear. Here, we utilize in vitro reconstitution of purified motor proteins and non-enzymatic microtubule-associated proteins (MAPs) to demonstrate that MAPs exhibit distinct influences on the motility of the three main classes of transport motors: kinesin-1, kinesin-3, and cytoplasmic dynein. Further, we dissect how combinations of MAPs affect motors and unveil MAP9 as a positive modulator of kinesin-3 motility. From these data, we propose a general "MAP code" that has the capacity to strongly bias directed movement along microtubules and helps elucidate the intricate intracellular sorting observed in highly polarized cells such as neurons.
许多真核细胞通过沿着微管轨道的分子马达驱动的调节主动运输来不对称地分配其细胞内成分。虽然存在内在和外在的马达活性调节,但在细胞内激活的马达-货物复合物的整体分布由什么决定仍不清楚。在这里,我们利用纯化的马达蛋白和非酶微管相关蛋白(MAPs)的体外重构来证明 MAPs 对三种主要类型的运输马达(驱动蛋白-1、驱动蛋白-3 和细胞质动力蛋白)的运动具有不同的影响。此外,我们剖析了 MAPs 如何影响马达,并揭示了 MAP9 是驱动蛋白-3 运动的正调节剂。根据这些数据,我们提出了一个通用的“MAP 密码”,它具有强烈偏向沿微管定向运动的能力,并有助于阐明在高度极化的细胞(如神经元)中观察到的复杂的细胞内分拣。