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The Interaction Between Lentiviral Integrase and LEDGF: Structural and Functional Insights

Since its initial description as an HIV-1 integrase (IN) interactor seven years ago, LEDGF has become one of the best-characterized host factors involved in viral replication. Results of intensive studies in several laboratories indicated that the protein serves as a targeting factor for the lentivi...

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Autores principales: Hare, Stephen, Cherepanov, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185499/
https://www.ncbi.nlm.nih.gov/pubmed/21994569
http://dx.doi.org/10.3390/v1030780
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author Hare, Stephen
Cherepanov, Peter
author_facet Hare, Stephen
Cherepanov, Peter
author_sort Hare, Stephen
collection PubMed
description Since its initial description as an HIV-1 integrase (IN) interactor seven years ago, LEDGF has become one of the best-characterized host factors involved in viral replication. Results of intensive studies in several laboratories indicated that the protein serves as a targeting factor for the lentiviral DNA integration machinery, and accounts for the characteristic preference of Lentivirus to integrate within active transcription units. The IN-LEDGF interaction has been put forward as a promising target for antiretroviral drug development and as a potential tool to improve safety of lentiviral vectors for use in gene therapy. Additionally, as a natural ligand of lentiviral IN proteins, LEDGF has been successfully used in structural biology studies of retroviral DNA integration. This review focuses on the structural aspects of the IN-LEDGF interaction and their functional consequences.
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spelling pubmed-31854992011-10-12 The Interaction Between Lentiviral Integrase and LEDGF: Structural and Functional Insights Hare, Stephen Cherepanov, Peter Viruses Review Since its initial description as an HIV-1 integrase (IN) interactor seven years ago, LEDGF has become one of the best-characterized host factors involved in viral replication. Results of intensive studies in several laboratories indicated that the protein serves as a targeting factor for the lentiviral DNA integration machinery, and accounts for the characteristic preference of Lentivirus to integrate within active transcription units. The IN-LEDGF interaction has been put forward as a promising target for antiretroviral drug development and as a potential tool to improve safety of lentiviral vectors for use in gene therapy. Additionally, as a natural ligand of lentiviral IN proteins, LEDGF has been successfully used in structural biology studies of retroviral DNA integration. This review focuses on the structural aspects of the IN-LEDGF interaction and their functional consequences. Molecular Diversity Preservation International (MDPI) 2009-11-06 /pmc/articles/PMC3185499/ /pubmed/21994569 http://dx.doi.org/10.3390/v1030780 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Hare, Stephen
Cherepanov, Peter
The Interaction Between Lentiviral Integrase and LEDGF: Structural and Functional Insights
title The Interaction Between Lentiviral Integrase and LEDGF: Structural and Functional Insights
title_full The Interaction Between Lentiviral Integrase and LEDGF: Structural and Functional Insights
title_fullStr The Interaction Between Lentiviral Integrase and LEDGF: Structural and Functional Insights
title_full_unstemmed The Interaction Between Lentiviral Integrase and LEDGF: Structural and Functional Insights
title_short The Interaction Between Lentiviral Integrase and LEDGF: Structural and Functional Insights
title_sort interaction between lentiviral integrase and ledgf: structural and functional insights
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185499/
https://www.ncbi.nlm.nih.gov/pubmed/21994569
http://dx.doi.org/10.3390/v1030780
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