| Literature DB >> 33462517 |
Jinwoo Lee1,2,3, Alex J B Kreutzberger1,2, Laura Odongo1,2, Elizabeth A Nelson1,4, David A Nyenhuis1,5, Volker Kiessling1,2, Binyong Liang1,2, David S Cafiso1,5, Judith M White1,4, Lukas K Tamm6,7.
Abstract
Cholesterol serves critical roles in enveloped virus fusion by modulating membrane properties. The glycoprotein (GP) of Ebola virus (EBOV) promotes fusion in the endosome, a process that requires the endosomal cholesterol transporter NPC1. However, the role of cholesterol in EBOV fusion is unclear. Here we show that cholesterol in GP-containing membranes enhances fusion and the membrane-proximal external region and transmembrane (MPER/TM) domain of GP interacts with cholesterol via several glycine residues in the GP2 TM domain, notably G660. Compared to wild-type (WT) counterparts, a G660L mutation caused a more open angle between MPER and TM domains in an MPER/TM construct, higher probability of stalling at hemifusion for GP2 proteoliposomes and lower cell entry of virus-like particles (VLPs). VLPs with depleted cholesterol show reduced cell entry, and VLPs produced under cholesterol-lowering statin conditions show less frequent entry than respective controls. We propose that cholesterol-TM interactions affect structural features of GP2, thereby facilitating fusion and cell entry.Entities:
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Year: 2021 PMID: 33462517 PMCID: PMC7992113 DOI: 10.1038/s41594-020-00548-4
Source DB: PubMed Journal: Nat Struct Mol Biol ISSN: 1545-9985 Impact factor: 15.369