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Tubulin and CRMP-2 complex is transported via Kinesin-1.

机译:微管蛋白和CRMP-2复合物通过Kinesin-1转运。

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摘要

Abstract The transport of tubulin and microtubules in a growing axon is essential for axonal growth and maintenance. However, the molecular mechanism underlying the linkage of tubulin and microtubules to motor proteins is not yet clear. Collapsin response mediator protein-2 (CRMP-2) is enriched at the distal part of growing axons in primary hippocampal neurons and plays a critical role in axon differentiation through its interaction with tubulin dimer and Numb. In this study, we show that CRMP-2 regulates tubulin transport by linking tubulin and Kinesin-1. The C-terminal region of CRMP-2 directly binds to the tetratricopeptide repeat domain of kinesin light chain 1 (KLC1). Soluble tubulin binds to the middle of CRMP-2 and forms a trimeric complex with CRMP-2/KLC1. Furthermore, the movement of GFP-tubulin in the photobleached area is weakened by knockdown of KLCs or CRMP-2. These results indicate that the CRMP-2/Kinesin-1 complex regulates soluble tubulin transport to the distal part of the growing axon.
机译:摘要微管蛋白和微管在不断增长的轴突中的运输对于轴突的生长和维持至关重要。然而,微管蛋白和微管连接到运动蛋白的分子机制尚不清楚。胶原蛋白介导蛋白2(CRMP-2)在原代海马神经元中生长的轴突的远端富集,并通过与微管蛋白二聚体和Numb的相互作用在轴突分化中起关键作用。在这项研究中,我们表明CRMP-2通过连接微管蛋白和Kinesin-1来调节微管蛋白的运输。 CRMP-2的C末端区域直接结合到驱动蛋白轻链1(KLC1)的四三肽重复域上。可溶性微管蛋白结合到CRMP-2的中间并与CRMP-2 / KLC1形成三聚体复合物。此外,KCLs或CRMP-2的敲低削弱了GFP-微管蛋白在光漂白区的运动。这些结果表明,CRMP-2 / Kinesin-1复合物调节可溶性微管蛋白向生长轴突远端的转运。

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