Structural basis of wedging the Golgi membrane by FAPP pleckstrin homology domains
Research output: Contribution to journal › Research article › Contributed › peer-review
Contributors
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
Original language | English |
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Pages (from-to) | 279-284 |
Number of pages | 6 |
Journal | EMBO reports |
Volume | 11 |
Issue number | 4 |
Publication status | Published - Apr 2010 |
Peer-reviewed | Yes |
Externally published | Yes |
External IDs
WOS | 000276117100012 |
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Scopus | 77950370938 |
PubMed | 20300118 |
ORCID | /0000-0003-2083-0506/work/148607251 |
Keywords
ASJC Scopus subject areas
Keywords
- Golgi trafficking, Membrane recognition, NMR spectroscopy, PH domain, Phosphatidylinositol 4-phosphate