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Inhibiting the HIV Integration Process: Past, Present, and the Future
[Image: see text] HIV integrase (IN) catalyzes the insertion into the genome of the infected human cell of viral DNA produced by the retrotranscription process. The discovery of raltegravir validated the existence of the IN, which is a new target in the field of anti-HIV drug research. The mechanism...
Autor principal: | |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926363/ https://www.ncbi.nlm.nih.gov/pubmed/24025027 http://dx.doi.org/10.1021/jm400674a |
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author | Di Santo, Roberto |
author_facet | Di Santo, Roberto |
author_sort | Di Santo, Roberto |
collection | PubMed |
description | [Image: see text] HIV integrase (IN) catalyzes the insertion into the genome of the infected human cell of viral DNA produced by the retrotranscription process. The discovery of raltegravir validated the existence of the IN, which is a new target in the field of anti-HIV drug research. The mechanism of catalysis of IN is depicted, and the characteristics of the inhibitors of the catalytic site of this viral enzyme are reported. The role played by the resistance is elucidated, as well as the possibility of bypassing this problem. New approaches to block the integration process are depicted as future perspectives, such as development of allosteric IN inhibitors, dual inhibitors targeting both IN and other enzymes, inhibitors of enzymes that activate IN, activators of IN activity, as well as a gene therapy approach. |
format | Online Article Text |
id | pubmed-3926363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39263632014-02-17 Inhibiting the HIV Integration Process: Past, Present, and the Future Di Santo, Roberto J Med Chem [Image: see text] HIV integrase (IN) catalyzes the insertion into the genome of the infected human cell of viral DNA produced by the retrotranscription process. The discovery of raltegravir validated the existence of the IN, which is a new target in the field of anti-HIV drug research. The mechanism of catalysis of IN is depicted, and the characteristics of the inhibitors of the catalytic site of this viral enzyme are reported. The role played by the resistance is elucidated, as well as the possibility of bypassing this problem. New approaches to block the integration process are depicted as future perspectives, such as development of allosteric IN inhibitors, dual inhibitors targeting both IN and other enzymes, inhibitors of enzymes that activate IN, activators of IN activity, as well as a gene therapy approach. American Chemical Society 2013-09-11 2014-02-13 /pmc/articles/PMC3926363/ /pubmed/24025027 http://dx.doi.org/10.1021/jm400674a Text en Copyright © 2013 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Di Santo, Roberto Inhibiting the HIV Integration Process: Past, Present, and the Future |
title | Inhibiting the HIV Integration
Process: Past, Present,
and the Future |
title_full | Inhibiting the HIV Integration
Process: Past, Present,
and the Future |
title_fullStr | Inhibiting the HIV Integration
Process: Past, Present,
and the Future |
title_full_unstemmed | Inhibiting the HIV Integration
Process: Past, Present,
and the Future |
title_short | Inhibiting the HIV Integration
Process: Past, Present,
and the Future |
title_sort | inhibiting the hiv integration
process: past, present,
and the future |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926363/ https://www.ncbi.nlm.nih.gov/pubmed/24025027 http://dx.doi.org/10.1021/jm400674a |
work_keys_str_mv | AT disantoroberto inhibitingthehivintegrationprocesspastpresentandthefuture |