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Development of peptide inhibitors of HIV transmission
Treatment of HIV has long faced the challenge of high mutation rates leading to rapid development of resistance, with ongoing need to develop new methods to effectively fight the infection. Traditionally, early HIV medications were designed to inhibit RNA replication and protein production through s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883972/ https://www.ncbi.nlm.nih.gov/pubmed/29744399 http://dx.doi.org/10.1016/j.bioactmat.2016.09.004 |
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author | Shi, Siyu Nguyen, Peter K. Cabral, Henry J. Diez-Barroso, Ramon Derry, Paul J. Kanahara, Satoko M. Kumar, Vivek A. |
author_facet | Shi, Siyu Nguyen, Peter K. Cabral, Henry J. Diez-Barroso, Ramon Derry, Paul J. Kanahara, Satoko M. Kumar, Vivek A. |
author_sort | Shi, Siyu |
collection | PubMed |
description | Treatment of HIV has long faced the challenge of high mutation rates leading to rapid development of resistance, with ongoing need to develop new methods to effectively fight the infection. Traditionally, early HIV medications were designed to inhibit RNA replication and protein production through small molecular drugs. Peptide based therapeutics are a versatile, promising field in HIV therapy, which continues to develop as we expand our understanding of key protein-protein interactions that occur in HIV replication and infection. This review begins with an introduction to HIV, followed by the biological basis of disease, current clinical management of the disease, therapeutics on the market, and finally potential avenues for improved drug development. |
format | Online Article Text |
id | pubmed-5883972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-58839722018-05-09 Development of peptide inhibitors of HIV transmission Shi, Siyu Nguyen, Peter K. Cabral, Henry J. Diez-Barroso, Ramon Derry, Paul J. Kanahara, Satoko M. Kumar, Vivek A. Bioact Mater Bioactive polymers and gel Treatment of HIV has long faced the challenge of high mutation rates leading to rapid development of resistance, with ongoing need to develop new methods to effectively fight the infection. Traditionally, early HIV medications were designed to inhibit RNA replication and protein production through small molecular drugs. Peptide based therapeutics are a versatile, promising field in HIV therapy, which continues to develop as we expand our understanding of key protein-protein interactions that occur in HIV replication and infection. This review begins with an introduction to HIV, followed by the biological basis of disease, current clinical management of the disease, therapeutics on the market, and finally potential avenues for improved drug development. KeAi Publishing 2016-09-16 /pmc/articles/PMC5883972/ /pubmed/29744399 http://dx.doi.org/10.1016/j.bioactmat.2016.09.004 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Bioactive polymers and gel Shi, Siyu Nguyen, Peter K. Cabral, Henry J. Diez-Barroso, Ramon Derry, Paul J. Kanahara, Satoko M. Kumar, Vivek A. Development of peptide inhibitors of HIV transmission |
title | Development of peptide inhibitors of HIV transmission |
title_full | Development of peptide inhibitors of HIV transmission |
title_fullStr | Development of peptide inhibitors of HIV transmission |
title_full_unstemmed | Development of peptide inhibitors of HIV transmission |
title_short | Development of peptide inhibitors of HIV transmission |
title_sort | development of peptide inhibitors of hiv transmission |
topic | Bioactive polymers and gel |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883972/ https://www.ncbi.nlm.nih.gov/pubmed/29744399 http://dx.doi.org/10.1016/j.bioactmat.2016.09.004 |
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