Flavivirus NS1 Structures Reveal Surfaces for Associations with Membranes and the Immune System

Author:

Akey David L.1,Brown W. Clay1,Dutta Somnath1,Konwerski Jamie1,Jose Joyce2,Jurkiw Thomas J.1,DelProposto James1,Ogata Craig M.3,Skiniotis Georgios14,Kuhn Richard J.25,Smith Janet L.14

Affiliation:

1. Life Sciences Institute, University of Michigan, Ann Arbor, MI 48109, USA.

2. Department of Biological Sciences, Purdue University, West Lafayette, IN 47907, USA.

3. GM/CA @ APS, Advanced Photon Source, Argonne National Laboratory, Argonne, IL 60439, USA.

4. Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.

5. Bindley Bioscience Center, Purdue University, West Lafayette, IN 47907, USA.

Abstract

Two-Faced Viral Protein Flaviviruses cause human diseases such as West Nile fever and dengue fever. The flavivirus nonstructural protein 1 (NS1) has multiple functions in flavivirus biology and is a target for vaccine development. Dimeric NS1 is essential for replication of the viral genome inside host cells, while hexameric NS1 is secreted and plays a role in evasion of the immune system. Akey et al. (p. 881 , published online 6 February; see the Perspective by Shi ) report crystal structures for full-length glycosylated NS1 from West Nile and dengue viruses. The structures show a hexamer comprised of three dimers. The structural analysis together with liposome and mutational studies identify a membrane interacting surface on one face of the dimer and an immune evasion surface on the other.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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