Lenacapavir allosterically remodels the HIV-1 capsid

Lenacapavir (LEN) is a highly potent, long-acting HIV-1 capsid inhibitor that holds exceptional promise for pre-exposure prophylaxis. LEN causes the mature viral capsid to rupture and lose integrity, but the underlying mechanism has been unclear. Here, we show that LEN is an allosteric modulator of HIV-1 capsid structure that breaks the capsid's fullerene cone architecture in two steps: loss of high-curvature declinations occurs early, followed by failure of the capsid body. At the molecular level, LEN alters the non-covalent bonding interactions between capsid subunits and reduces local lattice curvature. LEN also alters the material properties of the capsid, by increasing brittleness. These results provide molecular rationales for how LEN remodels HIV-1 capsid structure and impairs the replication capacity of the virus.

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Publication Details

Journal
Science Advances
Published
2026-09-02
DOI
https://doi.org/10.1126/sciadv.aed8384
Citations
7
Primary Topic
HIV Research and Treatment
Type
article
Field-Weighted Citation Impact
36.20

Funders

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article

Lenacapavir allosterically remodels the HIV-1 capsid

Owen Pornillos, Miguel J. B. Pereira, Wesley I. Sundquist, Devin E. Christensen et al.
7 citations
Science Advances
HIV Research and Treatment
36.20
article

Lenacapavir allosterically remodels the HIV-1 capsid

Owen Pornillos, Miguel J. B. Pereira, Wesley I. Sundquist, Devin E. Christensen, Jacob A. Lewis, Barbie K. Ganser-Pornillos, Nayara F. B. dos Santos, Owen Pornillos, Mason Hansen, Miguel J. B. Pereira
article en
7 citations

Abstract

Lenacapavir (LEN) is a highly potent, long-acting HIV-1 capsid inhibitor that holds exceptional promise for pre-exposure prophylaxis. LEN causes the mature viral capsid to rupture and lose integrity, but the underlying mechanism has been unclear. Here, we show that LEN is an allosteric modulator of HIV-1 capsid structure that breaks the capsid's fullerene cone architecture in two steps: loss of high-curvature declinations occurs early, followed by failure of the capsid body. At the molecular level, LEN alters the non-covalent bonding interactions between capsid subunits and reduces local lattice curvature. LEN also alters the material properties of the capsid, by increasing brittleness. These results provide molecular rationales for how LEN remodels HIV-1 capsid structure and impairs the replication capacity of the virus.

Science AdvancesVol. 12(36)
Spencer Foundation (US)
National Institutes of Health, National Institute of Allergy and Infectious Diseases
Good health and well-being
Openalex Percentile: Top 0%
HIV Research and Treatment
36.20
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