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Structural Insight into Eukaryotic Sterol Transport through Niemann-Pick Type C Proteins.

Cell (2019-09-24)
Mikael B L Winkler, Rune T Kidmose, Maria Szomek, Katja Thaysen, Shaun Rawson, Stephen P Muench, Daniel Wüstner, Bjørn Panyella Pedersen
ZUSAMMENFASSUNG

Niemann-Pick type C (NPC) proteins are essential for sterol homeostasis, believed to drive sterol integration into the lysosomal membrane before redistribution to other cellular membranes. Here, using a combination of crystallography, cryo-electron microscopy, and biochemical and in vivo studies on the Saccharomyces cerevisiae NPC system (NCR1 and NPC2), we present a framework for sterol membrane integration. Sterols are transferred between hydrophobic pockets of vacuolar NPC2 and membrane-protein NCR1. NCR1 has its N-terminal domain (NTD) positioned to deliver a sterol to a tunnel connecting NTD to the luminal membrane leaflet 50 Å away. A sterol is caught inside this tunnel during transport, and a proton-relay network of charged residues in the transmembrane region is linked to this tunnel supporting a proton-driven transport mechanism. We propose a model for sterol integration that clarifies the role of NPC proteins in this essential eukaryotic pathway and that rationalizes mutations in patients with Niemann-Pick disease type C.

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Sigma-Aldrich
Triton X-100, laboratory grade
Sigma-Aldrich
Thrombin aus Rinderplasma, lyophilized powder, ≥2,000 NIH units/mg protein (E1%/280 = 19.5)
Sigma-Aldrich
PNGase F aus Elizabethkingia meningoseptica, BioReagent, ≥95% (SDS-PAGE), for proteomics
Sigma-Aldrich
1,2-Dioleoyl-sn-Glycero-3-Phosphocholin, lyophilized powder