CryoEM structure of adenovirus type 3 fibre with desmoglein 2 shows an unusual mode of receptor engagement.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
12 03 2019
Historique:
received: 05 11 2018
accepted: 26 02 2019
entrez: 14 3 2019
pubmed: 14 3 2019
medline: 6 4 2019
Statut: epublish

Résumé

Attachment of human adenovirus (HAd) to the host cell is a critical step of infection. Initial attachment occurs via the adenoviral fibre knob protein and a cellular receptor. Here we report the cryo-electron microscopy (cryo-EM) structure of a <100 kDa non-symmetrical complex comprising the trimeric HAd type 3 fibre knob (HAd3K) and human desmoglein 2 (DSG2). The structure reveals a unique stoichiometry of 1:1 and 2:1 (DSG2: knob trimer) not previously observed for other HAd-receptor complexes. We demonstrate that mutating Asp261 in the fibre knob is sufficient to totally abolish receptor binding. These data shed new light on adenovirus infection strategies and provide insights for adenoviral vector development and structure-based design.

Identifiants

pubmed: 30862836
doi: 10.1038/s41467-019-09220-y
pii: 10.1038/s41467-019-09220-y
pmc: PMC6414520
doi:

Substances chimiques

Capsid Proteins 0
DSG2 protein, human 0
Desmoglein 2 0
Receptors, Virus 0
Recombinant Proteins 0
hexon capsid protein, Adenovirus 0
Asparagine 7006-34-0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1181

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Auteurs

Emilie Vassal-Stermann (E)

Institut de Biologie Structurale (IBS), Université Grenoble Alpes, CNRS, CEA, 71 Avenue des Martyrs, 38042, Grenoble, France.

Gregory Effantin (G)

Institut de Biologie Structurale (IBS), Université Grenoble Alpes, CNRS, CEA, 71 Avenue des Martyrs, 38042, Grenoble, France.

Chloe Zubieta (C)

Laboratoire de Physiologie Cellulaire et Végétale, Biosciences and Biotechnology Institute of Grenoble, UMR5168, CNRS/CEA/INRA/UGA, 17 Rue des Martyrs, 38054, Grenoble, France.

Wim Burmeister (W)

Institut de Biologie Structurale (IBS), Université Grenoble Alpes, CNRS, CEA, 71 Avenue des Martyrs, 38042, Grenoble, France.

Frédéric Iseni (F)

Unité de Virologie, Institut de Recherche Biomédicale des Armées, BP 73, 91223, Brétigny-sur-Orge Cedex, France.

Hongjie Wang (H)

Department of Medicine, Division of Medical Genetics, University of Washington, Box 357720, Seattle, WA, 98195, USA.

André Lieber (A)

Department of Medicine, Division of Medical Genetics, University of Washington, Box 357720, Seattle, WA, 98195, USA. lieber00@u.washington.edu.

Guy Schoehn (G)

Institut de Biologie Structurale (IBS), Université Grenoble Alpes, CNRS, CEA, 71 Avenue des Martyrs, 38042, Grenoble, France.

Pascal Fender (P)

Institut de Biologie Structurale (IBS), Université Grenoble Alpes, CNRS, CEA, 71 Avenue des Martyrs, 38042, Grenoble, France. pascal.fender@ibs.fr.

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Classifications MeSH