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驱动蛋白-2的β-发夹基序对其运动的调节。

Regulation of kinesin-2 motility by its β-hairpin motif.

作者信息

Webb Stephanie, Toropova Katerina, Mukhopadhyay Aakash G, Nofal Stephanie D, Roberts Anthony J

机构信息

Institute of Structural and Molecular Biology, Birkbeck, University of London, London, UK.

Sir William Dunn School of Pathology, University of Oxford, Oxford, UK.

出版信息

Nat Struct Mol Biol. 2025 Jul 29. doi: 10.1038/s41594-025-01630-5.

Abstract

Members of the kinesin-2 family coordinate with other motors to power diverse physiological processes, but the structural mechanisms regulating kinesin-2 activity have been unknown. Distinctively, kinesin-2s canonically function as heterotrimers of two different motor subunits (for example Kif3A and Kif3B in humans) and Kap3, but the role of heterotrimerization has yet to fully emerge. Here, we combine structural, cell biological and single-molecule approaches to dissect kinesin-2 regulation as a heterodimer, heterotrimer and quaternary complex with a cargo adaptor (APC). We identify a conserved motif in the tail of kinesin-2s (the β-hairpin motif) that, in conjunction with the adjacent coiled coil, controls kinesin-2 motility by sequestering the motor domains away from their microtubule track. Our data reveal how Kap3 binds via a multipartite interface with Kif3A and Kif3B. Rather than activating motility directly, Kap3 provides a platform on which cargo adaptors can engage and occlude the β-hairpin motif. Together, these data articulate a structural framework for kinesin-2 activation, recycling by dynein and adaptation for different biological functions.

摘要

驱动蛋白-2家族的成员与其他分子马达协同作用,为多种生理过程提供动力,但调节驱动蛋白-2活性的结构机制尚不清楚。特别的是,驱动蛋白-2通常作为由两个不同的马达亚基(例如人类中的Kif3A和Kif3B)和Kap3组成的异源三聚体发挥作用,但异源三聚化的作用尚未完全明确。在这里,我们结合结构生物学、细胞生物学和单分子方法,将驱动蛋白-2作为异源二聚体、异源三聚体以及与货物衔接蛋白(APC)形成的四聚体复合物来剖析其调控机制。我们在驱动蛋白-2的尾部鉴定出一个保守基序(β-发夹基序),该基序与相邻的卷曲螺旋一起,通过将马达结构域与微管轨道分离来控制驱动蛋白-2的运动性。我们的数据揭示了Kap3如何通过一个多部分界面与Kif3A和Kif3B结合。Kap3并非直接激活运动性,而是提供了一个平台,货物衔接蛋白可以在该平台上结合并封闭β-发夹基序。总之,这些数据阐明了驱动蛋白-2激活、动力蛋白介导的回收利用以及适应不同生物学功能的结构框架。

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