Structural basis of wedging the Golgi membrane by FAPP pleckstrin homology domains

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Marc Lenoir - , University of Birmingham (Autor:in)
  • Ünal Coskun - , Max Planck Institute of Molecular Cell Biology and Genetics (Autor:in)
  • Michal Grzybek - , Max Planck Institute of Molecular Cell Biology and Genetics (Autor:in)
  • Xinwang Cao - , Max Planck Institute of Molecular Cell Biology and Genetics (Autor:in)
  • Sabine B. Buschhorn - , Max Planck Institute of Molecular Cell Biology and Genetics (Autor:in)
  • Jonathan James - , University of Birmingham (Autor:in)
  • Kai Simons - , Max Planck Institute of Molecular Cell Biology and Genetics (Autor:in)
  • Michael Overduin - , University of Birmingham (Autor:in)

Abstract

The mechanisms underlying Golgi targeting and vesiculation are unknown, although the responsible phosphatidylinositol 4-phosphate (PtdIns(4)P) ligand and four-phosphate-adaptor protein (FAPP) modules have been defined. The micelle-bound structure of the FAPP1 pleckstrin homology domain reveals how its prominent wedge independently tubulates Golgi membranes by leaflet penetration. Mutations compromising the exposed hydrophobicity of full-length FAPP2 abolish lipid monolayer binding and compression. The trafficking process begins with an electrostatic approach, phosphoinositide sampling and perpendicular penetration. Extensive protein contacts with PtdIns(4)P and neighbouring phospholipids reshape the bilayer and initiate tubulation through a conserved wedge with features shared by diverse protein modules.

Details

OriginalspracheEnglisch
Seiten (von - bis)279-284
Seitenumfang6
FachzeitschriftEMBO reports
Jahrgang11
Ausgabenummer4
PublikationsstatusVeröffentlicht - Apr. 2010
Peer-Review-StatusJa
Extern publiziertJa

Externe IDs

WOS 000276117100012
Scopus 77950370938
PubMed 20300118
ORCID /0000-0003-2083-0506/work/148607251

Schlagworte

ASJC Scopus Sachgebiete

Schlagwörter

  • Golgi trafficking, Membrane recognition, NMR spectroscopy, PH domain, Phosphatidylinositol 4-phosphate

Bibliotheksschlagworte