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Short Linear Sequence Motif LxxPTPh Targets Diverse Proteins to Growing Microtubule Ends.
Kumar, Anil; Manatschal, Cristina; Rai, Ankit; Grigoriev, Ilya; Degen, Miriam Steiner; Jaussi, Rolf; Kretzschmar, Ines; Prota, Andrea E; Volkmer, Rudolf; Kammerer, Richard A; Akhmanova, Anna; Steinmetz, Michel O.
Afiliação
  • Kumar A; Laboratory of Biomolecular Research, Division of Biology and Chemistry, Paul Scherrer Institut, 5232 Villigen PSI, Switzerland.
  • Manatschal C; Laboratory of Biomolecular Research, Division of Biology and Chemistry, Paul Scherrer Institut, 5232 Villigen PSI, Switzerland.
  • Rai A; Cell Biology, Faculty of Science, Utrecht University, 3584 CH Utrecht, the Netherlands.
  • Grigoriev I; Cell Biology, Faculty of Science, Utrecht University, 3584 CH Utrecht, the Netherlands.
  • Degen MS; Laboratory of Biomolecular Research, Division of Biology and Chemistry, Paul Scherrer Institut, 5232 Villigen PSI, Switzerland.
  • Jaussi R; Laboratory of Biomolecular Research, Division of Biology and Chemistry, Paul Scherrer Institut, 5232 Villigen PSI, Switzerland.
  • Kretzschmar I; Institut für Medizinische Immunologie, Charité-Universitätsmedizin Berlin, Leibniz-Institut für Molekulare Pharmakologie, 10117 Berlin, Germany.
  • Prota AE; Laboratory of Biomolecular Research, Division of Biology and Chemistry, Paul Scherrer Institut, 5232 Villigen PSI, Switzerland.
  • Volkmer R; Institut für Medizinische Immunologie, Charité-Universitätsmedizin Berlin, Leibniz-Institut für Molekulare Pharmakologie, 10117 Berlin, Germany.
  • Kammerer RA; Laboratory of Biomolecular Research, Division of Biology and Chemistry, Paul Scherrer Institut, 5232 Villigen PSI, Switzerland.
  • Akhmanova A; Cell Biology, Faculty of Science, Utrecht University, 3584 CH Utrecht, the Netherlands.
  • Steinmetz MO; Laboratory of Biomolecular Research, Division of Biology and Chemistry, Paul Scherrer Institut, 5232 Villigen PSI, Switzerland. Electronic address: michel.steinmetz@psi.ch.
Structure ; 25(6): 924-932.e4, 2017 06 06.
Article em En | MEDLINE | ID: mdl-28552577
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Proteínas de Saccharomyces cerevisiae / Proteínas Associadas aos Microtúbulos / Microtúbulos Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Nucleares / Proteínas de Saccharomyces cerevisiae / Proteínas Associadas aos Microtúbulos / Microtúbulos Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article