Lenacapavir allosterically remodels the HIV-1 capsid

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The paper investigates how lenacapavir, a potent long-acting HIV-1 capsid inhibitor, disrupts the structure of the mature HIV-1 capsid and thereby impairs viral replication, using molecular and structural analyses of capsid architecture. The authors find that lenacapavir acts as an allosteric modulator that breaks the capsid’s fullerene cone architecture in two steps, with early loss of high-curvature features followed by failure of the capsid body. Mechanistically, lenacapavir alters non-covalent interactions between capsid subunits, reduces local lattice curvature, and increases capsid brittleness. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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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. Competing Interest Statement The authors have declared no competing interest.

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last seen: 2026-05-20T01:45:00.602351+00:00