The HIV capsid mimics karyopherin engagement of FG-nucleoporins

C. F. Dickson, S. Hertel, A. J. Tuckwell, N. Li, J. Ruan, S. C. Al-Izzi, N. Ariotti, E. Sierecki, Y. Gambin, R. G. Morris, G. J. Towers, T. Böcking and D. A. Jacques ()
Additional contact information
C. F. Dickson: University of New South Wales
S. Hertel: University of New South Wales
A. J. Tuckwell: University of New South Wales
N. Li: University of New South Wales
J. Ruan: University of New South Wales
S. C. Al-Izzi: University of New South Wales
N. Ariotti: University of Queensland
E. Sierecki: University of New South Wales
Y. Gambin: University of New South Wales
R. G. Morris: University of New South Wales
G. J. Towers: University College London
T. Böcking: University of New South Wales
D. A. Jacques: University of New South Wales

Nature, 2024, vol. 626, issue 8000, 836-842

Abstract: Abstract HIV can infect non-dividing cells because the viral capsid can overcome the selective barrier of the nuclear pore complex and deliver the genome directly into the nucleus1,2. Remarkably, the intact HIV capsid is more than 1,000 times larger than the size limit prescribed by the diffusion barrier of the nuclear pore3. This barrier in the central channel of the nuclear pore is composed of intrinsically disordered nucleoporin domains enriched in phenylalanine–glycine (FG) dipeptides. Through multivalent FG interactions, cellular karyopherins and their bound cargoes solubilize in this phase to drive nucleocytoplasmic transport4. By performing an in vitro dissection of the nuclear pore complex, we show that a pocket on the surface of the HIV capsid similarly interacts with FG motifs from multiple nucleoporins and that this interaction licences capsids to penetrate FG-nucleoporin condensates. This karyopherin mimicry model addresses a key conceptual challenge for the role of the HIV capsid in nuclear entry and offers an explanation as to how an exogenous entity much larger than any known cellular cargo may be able to non-destructively breach the nuclear envelope.

Date: 2024
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DOI: 10.1038/s41586-023-06969-7

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