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EAP45 association with budding HIV ‐1: Kinetics and domain requirements

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Peer-reviewed

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Abstract

Abstract: A number of viruses including HIV use the ESCRT system to bud from the infected cell. We have previously confirmed biochemically that ESCRT‐II is involved in this process in HIV‐1 and have defined the molecular domains that are important for this. Here, using SNAP‐tag fluorescent labelling and both fixed and live cell imaging we show that the ESCRT‐II component EAP45 colocalises with the HIV protein Gag at the plasma membrane in a temporal and quantitative manner, similar to that previously shown for ALIX and Gag. We show evidence that a proportion of EAP45 may be packaged within virions, and we confirm the importance of the N terminus of EAP45 and specifically the H0 domain in this process. By contrast, the Glue domain of EAP45 is more critical for recruitment during cytokinesis, emphasising that viruses have ways of recruiting cellular components that may be distinct from those used by some cellular processes. This raises the prospect of selective interference with the pathway to inhibit viral function while leaving cellular functions relatively unperturbed.

Description

Funder: Gates Cambridge Scholarship


Funder: Infinitus China Ltd


Funder: MedImmune; Id: http://dx.doi.org/10.13039/501100004628


Funder: Microbiology Society; Id: http://dx.doi.org/10.13039/501100007901


Funder: RCUK Technology Touching Life Initiative

Journal Title

Traffic

Conference Name

Journal ISSN

1398-9219
1600-0854

Volume Title

Publisher

John Wiley & Sons A/S

Rights and licensing

Except where otherwised noted, this item's license is described as http://creativecommons.org/licenses/by/4.0/
Sponsorship
Engineering and Physical Sciences Research Council (EP/H018301/1, EP/L015889/1)
Medical Research Council (MR/K015850/1, MR/K02292X/1, MR/N0229939/1)
Wellcome Trust (089703/Z/09/Z, 203249/Z/16/Z)