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Comment
. 2019 Jun;20(6):668-669.
doi: 10.1038/s41590-019-0387-0.

Heavy metal protease takes a tiki torch to HIV assembly

Affiliations
Comment

Heavy metal protease takes a tiki torch to HIV assembly

Una O'Doherty et al. Nat Immunol. 2019 Jun.
No abstract available

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Conflict of interest statement

Competing interests

The authors declare no competing interests.

Figures

Fig. 1 |
Fig. 1 |. HIV-1 replication is blocked at multiple stages in resting CD4+ T cells.
a, Major steps in the HIV-1 replication cycle, including attachment and entry of the virus, reverse transcription, import into the nucleus, integration of viral DNA, expression of viral genes, export of RNA, particle assembly, incorporation of Env, and particle budding and maturation. The steps in red font have been shown before to occur inefficiently in resting CD4+ T cells relative to that in activated CD4+ T cells (as discussed in the text). CXCR4 and CCR5, co-receptors; Pol, HIV polymerase; PIC, pre-integration complex. b, Proposed model for the degradation of Gag at the plasma membrane by the Tiki-family metalloprotease TRABD2A (by Liang et al.). In this model, TRABD2A-induced degradation of Gag prevents the assembly of viral particles in resting CD4+ T cells and their release from those cells.

Comment on

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