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The capsid revolution
Ian A. Taylor1,* , Ariberto Fassati2,3,*
1Macromolecular Structure Laboratory, The Francis Crick Institute, London NW1 1AT, UK
2Division of Infection and Immunity, University College London, London WC1E 6JF, UK
3Institute of Immunity and Transplantation, University College London, London NW3 2PP, UK
*Correspondence to:Ian A. Taylor , Email:ian.taylor@crick.ac.uk Ariberto Fassati , Email:a.fassati@ucl.ac.uk
J Mol Cell Biol, Volume 15, Issue 11, November 2023, mjad076,  https://doi.org/10.1093/jmcb/mjad076
Keyword: HIV-1 capsid, CPSF6, Lenacapavir, integration, IP6, nucleus, reverse transcription

Lenacapavir, targeting the human immunodeficiency virus type-1 (HIV-1) capsid, is the first-in-class antiretroviral drug recently approved for clinical use. The development of Lenacapavir is attributed to the remarkable progress in our understanding of the capsid protein made during the last few years. Considered little more than a component of the virus shell to be shed early during infection, the capsid has been found to be a key player in the HIV-1 life cycle by interacting with multiple host factors, entering the nucleus, and directing integration. Here, we describe the key advances that led to this ‘capsid revolution’.