A new class of capsid-targeting inhibitors that specifically block HIV-1 nuclear import

HIV-1 capsids cross nuclear pore complexes (NPCs) by engaging with the nuclear import machinery. To identify compounds that inhibit HIV-1 nuclear import, we screened drugs in silico on a three-dimensional model of a CA hexamer bound by Transportin-1 (TRN-1). Among hits, compound H27 inhibited HIV-1 with a low micromolar IC<sub>50</sub>. Unlike other CA-targeting compounds, H27 did not alter CA assembly or disassembly, inhibited nuclear import specifically, and retained antiviral activity against PF74- and Lenacapavir-resistant mutants. The differential sensitivity of divergent primate lentiviral capsids, capsid stability and H27 escape mutants, together with structural analyses, suggest that H27 makes multiple low affinity contacts with assembled capsid. Interaction experiments indicate that H27 may act by preventing CA from engaging with components of the NPC machinery such as TRN-1. H27 exhibited good metabolic stability in vivo and was efficient against different subtypes and circulating recombinant forms from treatment-naïve patients as well as strains resistant to the four main classes of antiretroviral drugs. This work identifies compounds that demonstrate a novel mechanism of action by specifically blocking HIV-1 nuclear import.

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Publication Details

Journal
EMBO Molecular Medicine
Published
2024-10-02
DOI
https://doi.org/10.1038/s44321-024-00143-w
Citations
4
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
1.17

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article

A new class of capsid-targeting inhibitors that specifically block HIV-1 nuclear import

Célia Chamontin, Valérie Courgnaud, Ian A. Taylor, Laurent Chaloin et al.
4 citations
EMBO Molecular Medicine
HIV Research and Treatment
1.17
article

A new class of capsid-targeting inhibitors that specifically block HIV-1 nuclear import

Célia Chamontin, Valérie Courgnaud, Ian A. Taylor, Laurent Chaloin, Corinne Henriquet, Anne‐Geneviève Marcelin, Aude Boulay, Martine Pugnière, Mickaël Blaise, Nathalie J. Arhel, Isabelle Malet, Giuseppe Nicastro, Emmanuel Quevarec, S.D. Perrin
article en
4 citations

Abstract

HIV-1 capsids cross nuclear pore complexes (NPCs) by engaging with the nuclear import machinery. To identify compounds that inhibit HIV-1 nuclear import, we screened drugs in silico on a three-dimensional model of a CA hexamer bound by Transportin-1 (TRN-1). Among hits, compound H27 inhibited HIV-1 with a low micromolar IC<sub>50</sub>. Unlike other CA-targeting compounds, H27 did not alter CA assembly or disassembly, inhibited nuclear import specifically, and retained antiviral activity against PF74- and Lenacapavir-resistant mutants. The differential sensitivity of divergent primate lentiviral capsids, capsid stability and H27 escape mutants, together with structural analyses, suggest that H27 makes multiple low affinity contacts with assembled capsid. Interaction experiments indicate that H27 may act by preventing CA from engaging with components of the NPC machinery such as TRN-1. H27 exhibited good metabolic stability in vivo and was efficient against different subtypes and circulating recombinant forms from treatment-naïve patients as well as strains resistant to the four main classes of antiretroviral drugs. This work identifies compounds that demonstrate a novel mechanism of action by specifically blocking HIV-1 nuclear import.

EMBO Molecular MedicineVol. 16(11)
Centre National de la Recherche Scientifique (FR), Inserm (FR), The Francis Crick Institute (GB), Sorbonne Université (FR), Assistance Publique – Hôpitaux de Paris (FR), Institut de Génétique Moléculaire de Montpellier (FR), Pitié-Salpêtrière Hospital (FR), Institut de Recherche en Cancérologie de Montpellier (FR), Institut de Recherche en Infectiologie de Montpellier (FR)
Vanderbilt University, Sidaction, Wellcome Trust, Francis Crick Institute, Cancer Research UK, Agence Nationale de Recherches sur le Sida et les Hépatites Virales, Muséum National d'Histoire Naturelle, Université de Montpellier, Montpellier Université d'Excellence, Medical Research Council
Good health and well-being
Openalex Percentile: Top 21%
HIV Research and Treatment
1.17
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