IP6 is an HIV pocket factor that prevents capsid collapse and promotes DNA synthesis.
Mallery, Donna L
Márquez, Chantal L
Dickson, Claire F
Towers, Gregory J
eLife Sciences Publications, Ltd
MetadataShow full item record
Mallery, D. L., Márquez, C. L., McEwan, W., Dickson, C. F., Jacques, D. A., Anandapadamanaban, M., Bichel, K., et al. (2018). IP6 is an HIV pocket factor that prevents capsid collapse and promotes DNA synthesis.. Elife, 7 https://doi.org/10.7554/eLife.35335
The HIV capsid is semipermeable and covered in electropositive pores that are essential for viral DNA synthesis and infection. Here, we show that these pores bind the abundant cellular polyanion IP6, transforming viral stability from minutes to hours and allowing newly synthesised DNA to accumulate inside the capsid. An arginine ring within the pore coordinates IP6, which strengthens capsid hexamers by almost 10°C. Single molecule measurements demonstrate that this renders native HIV capsids highly stable and protected from spontaneous collapse. Moreover, encapsidated reverse transcription assays reveal that, once stabilised by IP6, the accumulation of new viral DNA inside the capsid increases >100 fold. Remarkably, isotopic labelling of inositol in virus-producing cells reveals that HIV selectively packages over 300 IP6 molecules per infectious virion. We propose that HIV recruits IP6 to regulate capsid stability and uncoating, analogous to picornavirus pocket factors. HIV-1/IP6/capsid/co-factor/reverse transcription.
Humans, HIV-1, Virion, Capsid, Polymers, Subtilisin, Nucleotides, DNA, Viral, Adenosine Triphosphate, Reverse Transcriptase Inhibitors, Virus Assembly, Reverse Transcription, HEK293 Cells
Wellcome Trust (206248/Z/17/Z)
External DOI: https://doi.org/10.7554/eLife.35335
This record's URL: https://www.repository.cam.ac.uk/handle/1810/283034
Attribution 4.0 International
Licence URL: https://creativecommons.org/licenses/by/4.0/