Structural Basis for Hijacking of Cellular LxxLL Motifs by Papillomavirus E6 Oncoproteins

Author:

Zanier Katia1,Charbonnier Sebastian1,Sidi Abdellahi Ould M'hamed Ould1,McEwen Alastair G.2,Ferrario Maria Giovanna2,Poussin-Courmontagne Pierre2,Cura Vincent2,Brimer Nicole3,Babah Khaled Ould1,Ansari Tina3,Muller Isabelle1,Stote Roland H.2,Cavarelli Jean2,Vande Pol Scott3,Travé Gilles1

Affiliation:

1. Biotechnologie et Signalisation Cellulaire UMR 7242, Ecole Supérieure de Biotechnologie de Strasbourg, Boulevard Sébastien Brant, BP 10413, F-67412 Illkirch, France.

2. Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC)/INSERM U964/CNRS UMR 7104/Université de Strasbourg, 1 rue Laurent Fries, BP 10142, F-67404 Illkirch, France.

3. Department of Pathology, University of Virginia, Post Office Box 800904, Charlottesville, VA 22908–0904, USA.

Abstract

Targeting HPV Papillomaviruses infect mammalian epithelial cells and induce cancers, including cervical cancer in humans. Vaccines against human papillomavirus (HPV) can prevent, but not cure, infection. A key viral oncoprotein, E6, acts by binding and inactivating many host proteins. Zanier et al. (p. 694 ) determined high-resolution crystal structures of bovine papillomavirus bound to a peptide from the focal adhesion protein, paxillin, and of HPV bound to a peptide from the ubiquitin ligase E6AP. The structures show that the peptide binds in a pocket formed by two zinc domains and a linker helix, which represents a promising target for therapeutics.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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