Towards Inhibition of Vif-APOBEC3G Interaction: Which Protein to Target?

APOBEC proteins appeared in the cellular battle against HIV-1 as part of intrinsic cellular immunity. The antiretroviral activity of some of these proteins is overtaken by the action of HIV-1 Viral Infectivity Factor (Vif) protein. Since the discovery of APOBEC3G (A3G) as an antiviral factor, many a...

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Main Authors: Iris Cadima-Couto, Joao Goncalves
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:Advances in Virology
Online Access:http://dx.doi.org/10.1155/2010/649315
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author Iris Cadima-Couto
Joao Goncalves
author_facet Iris Cadima-Couto
Joao Goncalves
author_sort Iris Cadima-Couto
collection DOAJ
description APOBEC proteins appeared in the cellular battle against HIV-1 as part of intrinsic cellular immunity. The antiretroviral activity of some of these proteins is overtaken by the action of HIV-1 Viral Infectivity Factor (Vif) protein. Since the discovery of APOBEC3G (A3G) as an antiviral factor, many advances have been made to understand its mechanism of action in the cell and how Vif acts in order to counteract its activity. The mainstream concept is that Vif overcomes the innate antiviral activity of A3G by direct protein binding and promoting its degradation via the cellular ubiquitin/proteasomal pathway. Vif may also inhibit A3G through mechanisms independent of proteasomal degradation. Binding of Vif to A3G is essential for its degradation since disruption of this interaction is predicted to stimulate intracellular antiviral immunity. In this paper we will discuss the different binding partners between both proteins as one of the major challenges for the development of new antiviral drugs.
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spelling doaj-art-6f7cd5b02ac94a628f8db093e29b7e242025-02-03T06:46:11ZengWileyAdvances in Virology1687-86391687-86472010-01-01201010.1155/2010/649315649315Towards Inhibition of Vif-APOBEC3G Interaction: Which Protein to Target?Iris Cadima-Couto0Joao Goncalves1URIA-Centro Patogénese Molecular and Instituto de Medicina Molecular, Faculdade de Farmácia da Universidade Lisboa, Avenue Das Forcas Armadas, 1649-019 Lisboa, PortugalURIA-Centro Patogénese Molecular and Instituto de Medicina Molecular, Faculdade de Farmácia da Universidade Lisboa, Avenue Das Forcas Armadas, 1649-019 Lisboa, PortugalAPOBEC proteins appeared in the cellular battle against HIV-1 as part of intrinsic cellular immunity. The antiretroviral activity of some of these proteins is overtaken by the action of HIV-1 Viral Infectivity Factor (Vif) protein. Since the discovery of APOBEC3G (A3G) as an antiviral factor, many advances have been made to understand its mechanism of action in the cell and how Vif acts in order to counteract its activity. The mainstream concept is that Vif overcomes the innate antiviral activity of A3G by direct protein binding and promoting its degradation via the cellular ubiquitin/proteasomal pathway. Vif may also inhibit A3G through mechanisms independent of proteasomal degradation. Binding of Vif to A3G is essential for its degradation since disruption of this interaction is predicted to stimulate intracellular antiviral immunity. In this paper we will discuss the different binding partners between both proteins as one of the major challenges for the development of new antiviral drugs.http://dx.doi.org/10.1155/2010/649315
spellingShingle Iris Cadima-Couto
Joao Goncalves
Towards Inhibition of Vif-APOBEC3G Interaction: Which Protein to Target?
Advances in Virology
title Towards Inhibition of Vif-APOBEC3G Interaction: Which Protein to Target?
title_full Towards Inhibition of Vif-APOBEC3G Interaction: Which Protein to Target?
title_fullStr Towards Inhibition of Vif-APOBEC3G Interaction: Which Protein to Target?
title_full_unstemmed Towards Inhibition of Vif-APOBEC3G Interaction: Which Protein to Target?
title_short Towards Inhibition of Vif-APOBEC3G Interaction: Which Protein to Target?
title_sort towards inhibition of vif apobec3g interaction which protein to target
url http://dx.doi.org/10.1155/2010/649315
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