| Literature DB >> 28552577 |
Anil Kumar1, Cristina Manatschal1, Ankit Rai2, Ilya Grigoriev2, Miriam Steiner Degen1, Rolf Jaussi1, Ines Kretzschmar3, Andrea E Prota1, Rudolf Volkmer3, Richard A Kammerer1, Anna Akhmanova2, Michel O Steinmetz4.
Abstract
Microtubule plus-end tracking proteins (+TIPs) are involved in virtually all microtubule-based processes. End-binding (EB) proteins are considered master regulators of +TIP interaction networks, since they autonomously track growing microtubule ends and recruit a plethora of proteins to this location. Two major EB-interacting elements have been described: CAP-Gly domains and linear SxIP sequence motifs. Here, we identified LxxPTPh as a third EB-binding motif that enables major +TIPs to interact with EBs at microtubule ends. In contrast to EB-SxIP and EB-CAP-Gly, the EB-LxxPTPh binding mode does not depend on the C-terminal tail region of EB. Our study reveals that +TIPs developed additional strategies besides CAP-Gly and SxIP to target EBs at growing microtubule ends. They further provide a unique basis to discover novel +TIPs, and to dissect the role of key interaction nodes and their differential regulation for hierarchical +TIP network organization and function in eukaryotic organisms.Entities:
Keywords: X-ray crystallography; end-binding proteins; linear motif; microtubule plus-end tracking proteins; molecular mechanism; structure-function relationship
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Year: 2017 PMID: 28552577 DOI: 10.1016/j.str.2017.04.010
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006