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Identifying Chemicals with Potential Therapy of HIV Based on Protein-Protein and Protein-Chemical Interaction Network
Acquired immune deficiency syndrome (AIDS) is a severe infectious disease that causes a large number of deaths every year. Traditional anti-AIDS drugs directly targeting the HIV-1 encoded enzymes including reverse transcriptase (RT), protease (PR) and integrase (IN) usually suffer from drug resistan...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675210/ https://www.ncbi.nlm.nih.gov/pubmed/23762317 http://dx.doi.org/10.1371/journal.pone.0065207 |
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author | Li, Bi-Qing Niu, Bing Chen, Lei Wei, Ze-Jun Huang, Tao Jiang, Min Lu, Jing Zheng, Ming-Yue Kong, Xiang-Yin Cai, Yu-Dong |
author_facet | Li, Bi-Qing Niu, Bing Chen, Lei Wei, Ze-Jun Huang, Tao Jiang, Min Lu, Jing Zheng, Ming-Yue Kong, Xiang-Yin Cai, Yu-Dong |
author_sort | Li, Bi-Qing |
collection | PubMed |
description | Acquired immune deficiency syndrome (AIDS) is a severe infectious disease that causes a large number of deaths every year. Traditional anti-AIDS drugs directly targeting the HIV-1 encoded enzymes including reverse transcriptase (RT), protease (PR) and integrase (IN) usually suffer from drug resistance after a period of treatment and serious side effects. In recent years, the emergence of numerous useful information of protein-protein interactions (PPI) in the HIV life cycle and related inhibitors makes PPI a new way for antiviral drug intervention. In this study, we identified 26 core human proteins involved in PPI between HIV-1 and host, that have great potential for HIV therapy. In addition, 280 chemicals that interact with three HIV drugs targeting human proteins can also interact with these 26 core proteins. All these indicate that our method as presented in this paper is quite promising. The method may become a useful tool, or at least plays a complementary role to the existing method, for identifying novel anti-HIV drugs. |
format | Online Article Text |
id | pubmed-3675210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36752102013-06-12 Identifying Chemicals with Potential Therapy of HIV Based on Protein-Protein and Protein-Chemical Interaction Network Li, Bi-Qing Niu, Bing Chen, Lei Wei, Ze-Jun Huang, Tao Jiang, Min Lu, Jing Zheng, Ming-Yue Kong, Xiang-Yin Cai, Yu-Dong PLoS One Research Article Acquired immune deficiency syndrome (AIDS) is a severe infectious disease that causes a large number of deaths every year. Traditional anti-AIDS drugs directly targeting the HIV-1 encoded enzymes including reverse transcriptase (RT), protease (PR) and integrase (IN) usually suffer from drug resistance after a period of treatment and serious side effects. In recent years, the emergence of numerous useful information of protein-protein interactions (PPI) in the HIV life cycle and related inhibitors makes PPI a new way for antiviral drug intervention. In this study, we identified 26 core human proteins involved in PPI between HIV-1 and host, that have great potential for HIV therapy. In addition, 280 chemicals that interact with three HIV drugs targeting human proteins can also interact with these 26 core proteins. All these indicate that our method as presented in this paper is quite promising. The method may become a useful tool, or at least plays a complementary role to the existing method, for identifying novel anti-HIV drugs. Public Library of Science 2013-06-06 /pmc/articles/PMC3675210/ /pubmed/23762317 http://dx.doi.org/10.1371/journal.pone.0065207 Text en © 2013 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Li, Bi-Qing Niu, Bing Chen, Lei Wei, Ze-Jun Huang, Tao Jiang, Min Lu, Jing Zheng, Ming-Yue Kong, Xiang-Yin Cai, Yu-Dong Identifying Chemicals with Potential Therapy of HIV Based on Protein-Protein and Protein-Chemical Interaction Network |
title | Identifying Chemicals with Potential Therapy of HIV Based on Protein-Protein and Protein-Chemical Interaction Network |
title_full | Identifying Chemicals with Potential Therapy of HIV Based on Protein-Protein and Protein-Chemical Interaction Network |
title_fullStr | Identifying Chemicals with Potential Therapy of HIV Based on Protein-Protein and Protein-Chemical Interaction Network |
title_full_unstemmed | Identifying Chemicals with Potential Therapy of HIV Based on Protein-Protein and Protein-Chemical Interaction Network |
title_short | Identifying Chemicals with Potential Therapy of HIV Based on Protein-Protein and Protein-Chemical Interaction Network |
title_sort | identifying chemicals with potential therapy of hiv based on protein-protein and protein-chemical interaction network |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675210/ https://www.ncbi.nlm.nih.gov/pubmed/23762317 http://dx.doi.org/10.1371/journal.pone.0065207 |
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