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  Cholesterol sensing by CD81 is important for hepatitis C virus entry

Palor, M., Stejskal, L., Mandal, P., Lenman, A., Alberione, M. P., Kirui, J., et al. (2020). Cholesterol sensing by CD81 is important for hepatitis C virus entry. Journal of Biological Chemistry, 295(50), 16931-16948. doi:10.1074/jbc.RA120.014761.

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Genre: Zeitschriftenartikel
Untertitel : Microbiology Protein Structure and Folding

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 Urheber:
Palor, Machaela, Autor
Stejskal, Lenka, Autor
Mandal, Piya, Autor
Lenman, Annasara, Autor
Alberione, Maria Pia, Autor
Kirui, Jared, Autor
Moeller, Rebecca, Autor
Ebner, Stefan1, Autor           
Meissner, Felix1, Autor           
Gerold, Gisa, Autor
Shepherd, Adrian J., Autor
Grove, Joe, Autor
Affiliations:
1Meissner, Felix / Experimental Systems Immunology, Max Planck Institute of Biochemistry, Max Planck Society, ou_2149678              

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Schlagwörter: SCAVENGER RECEPTOR-BI; TETRASPANIN-ENRICHED MICRODOMAINS; BROADLY NEUTRALIZING ANTIBODIES; E2 GLYCOPROTEIN; SR-BI; BINDING; IDENTIFICATION; INFECTION; DEFINES; ORGANIZATIONBiochemistry & Molecular Biology; cholesterol-binding protein; tetraspanin; plasma membrane; virus entry; hepatitis C virus (HCV); virus entry; molecular dynamics;
 Zusammenfassung: CD81 plays a central role in a variety of physiological and pathological processes. Recent structural analysis of CD81 indicates that it contains an intramembrane cholesterol-binding pocket and that interaction with cholesterol may regulate a conformational switch in the large extracellular domain of CD81. Therefore, CD81 possesses a potential cholesterol-sensing mechanism; however, its relevance for protein function is thus far unknown. In this study we investigate CD81 cholesterol sensing in the context of its activity as a receptor for hepatitis C virus (HCV). Structure-led mutagenesis of the cholesterol-binding pocket reduced CD81-cholesterol association but had disparate effects on HCV entry, both reducing and enhancing CD81 receptor activity. We reasoned that this could be explained by alterations in the consequences of cholesterol binding. To investigate this further we performed molecular dynamic simulations of CD81 with and without cholesterol; this identified a potential allosteric mechanism by which cholesterol binding regulates the conformation of CD81. To test this, we designed further mutations to force CD81 into either the open (cholesterol-unbound) or closed (cholesterol-bound) conformation. The open mutant of CD81 exhibited reduced HCV receptor activity, whereas the closed mutant enhanced activity. These data are consistent with cholesterol sensing switching CD81 between a receptor active and inactive state. CD81 interactome analysis also suggests that conformational switching may modulate the assembly of CD81-partner protein networks. This work furthers our understanding of the molecular mechanism of CD81 cholesterol sensing, how this relates to HCV entry, and CD81's function as a molecular scaffold; these insights are relevant to CD81's varied roles in both health and disease.

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Sprache(n): eng - English
 Datum: 2020-12
 Publikationsstatus: Erschienen
 Seiten: 18
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: ISI: 000599868700004
DOI: 10.1074/jbc.RA120.014761
 Art des Abschluß: -

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Titel: Journal of Biological Chemistry
  Andere : J. Biol. Chem.
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: Baltimore, etc. : American Society for Biochemistry and Molecular Biology [etc.]
Seiten: - Band / Heft: 295 (50) Artikelnummer: - Start- / Endseite: 16931 - 16948 Identifikator: ISSN: 0021-9258
CoNE: https://pure.mpg.de/cone/journals/resource/954925410826