Structural Insight into Eukaryotic Sterol Transport through Niemann-Pick Type C Proteins
Author(s) -
Mikael B. L. Winkler,
R.T. Kidmose,
Maria Szomek,
Katja Thaysen,
Shaun Rawson,
Stephen P. Muench,
Daniel Wüstner,
Bjørn Panyella Pedersen
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.08.038
Subject(s) - sterol , biology , saccharomyces cerevisiae , microbiology and biotechnology , transport protein , membrane protein , transmembrane protein , transmembrane domain , membrane , integral membrane protein , biochemistry , yeast , cholesterol , receptor
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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