Cryo-EM structures and atomic model of the HIV-1 strand transfer complex intasome

Author:

Passos Dario Oliveira1,Li Min2,Yang Renbin2,Rebensburg Stephanie V.3,Ghirlando Rodolfo2,Jeon Youngmin1,Shkriabai Nikoloz3,Kvaratskhelia Mamuka3,Craigie Robert2,Lyumkis Dmitry1

Affiliation:

1. Laboratory of Genetics and Helmsley Center for Genomic Medicine, The Salk Institute for Biological Studies, 10010 North Torrey Pines Road, La Jolla, CA 92037, USA.

2. Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

3. Center for Retrovirus Research and College of Pharmacy, The Ohio State University, Columbus, OH 43210, USA.

Abstract

High-resolution insights into the intasome An essential step in the life cycle of lentiviruses such as HIV-1 is when viral DNA integrates into the host genome, establishing a permanent infection of the host cell. The viral integrase enzyme catalyzes this process and is a major drug target. During viral integration, integrase binds the ends of viral DNA, forming a higher-order structure called the intasome. Passos et al. and Ballandras-Colas et al. used cryo—electron microscopy to solve the structures of the intasomes from HIV-1 and maedi-visna virus (ovine lentivirus), respectively. These structures reveal how integrase self-associates to form a functional intasome and help resolve previous conflicting models of intasome assembly. Science , this issue p. 89 , p. 93

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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