Molecular basis for assembly and activation of the Hook3 − KIF1C complex-dependent transport machinery
Hye Seon Lee, Daseuli Yu, Kyoung Eun Baek, Ho-Chul Shin, Seung Jun Kim, Won Do Heo, Bonsu Ku

TL;DR
This study reveals how Hook3 and KIF1C form a complex to enable anterograde cargo transport in cells, providing insights into the molecular mechanisms of microtubule-based transport.
Contribution
The study identifies the structural and functional basis for the Hook3-KIF1C complex and its role in cargo transport.
Findings
Hook3 and KIF1C form a 2:2 heterotetrameric complex essential for anterograde transport.
KIF1C competitively interacts with PTPN21 and Hook3, promoting its activation.
Interaction with KIF1C is necessary for Hook3-mediated transport in RPE1 cells.
Abstract
Microtubule-associated cargo transport, a central process governing the localization and movement of various cellular cargoes, is orchestrated by the coordination of two types of motor proteins (kinesins and dyneins), along with diverse adaptor and accessory proteins. Hook microtubule tethering protein 3 (Hook3) is a cargo adaptor that serves as a scaffold for recruiting kinesin family member 1C (KIF1C) and dynein, thereby regulating bidirectional cargo transport. Herein, we conduct structural and functional analyses of how Hook3 mediates KIF1C-dependent anterograde cargo transport through interaction with KIF1C and PTPN21. We verify the interactions among the three proteins and determine the crystal structure of the Hook3(553–624) − KIF1C(714–809) complex. Subsequent structure-based mutational analysis demonstrates that this complex formation is necessary and sufficient for the…
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Taxonomy
TopicsEnzyme Structure and Function · Microtubule and mitosis dynamics · Mechanisms of cancer metastasis
