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Inhibition of Ebola virus glycoprotein-mediated cytotoxicity by targeting its transmembrane domain and cholesterol
Uppsala universitet, Science for Life Laboratory, SciLifeLab. Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Biologiska sektionen, Institutionen för cell- och molekylärbiologi, Molekylär evolution.
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2015 (engelsk)Inngår i: Nature Communications, ISSN 2041-1723, E-ISSN 2041-1723, Vol. 6, artikkel-id 7688Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The high pathogenicity of the Ebola virus reflects multiple concurrent processes on infection. Among other important determinants, Ebola fusogenic glycoprotein (GP) has been associated with the detachment of infected cells and eventually leads to vascular leakage and haemorrhagic fever. Here we report that the membrane-anchored GP is sufficient to induce the detachment of adherent cells. The results show that the detachment induced through either full-length GP(1,2) or the subunit GP(2) depends on cholesterol and the structure of the transmembrane domain. These data reveal a novel molecular mechanism in which GP regulates Ebola virus assembly and suggest that cholesterol-reducing agents could be useful as therapeutics to counteract GP-mediated cell detachment.

sted, utgiver, år, opplag, sider
2015. Vol. 6, artikkel-id 7688
HSV kategori
Identifikatorer
URN: urn:nbn:se:uu:diva-261317DOI: 10.1038/ncomms8688ISI: 000358858100032PubMedID: 26158910OAI: oai:DiVA.org:uu-261317DiVA, id: diva2:851007
Tilgjengelig fra: 2015-09-03 Laget: 2015-09-01 Sist oppdatert: 2017-12-04bibliografisk kontrollert

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