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The Molecular Basis of pH-Modulated HIV gp120 Binding Revealed

Decades of research has yet to provide a vaccine for HIV, the virus which causes AIDS. Recent theoretical research has turned attention to mucosa pH levels over systemic pH levels. Previous research in this field developed a computational approach for determining pH sensitivity that indicated higher...

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Autores principales: Morton, Scott P, Phillips, Julie B, Phillips, Joshua L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407167/
https://www.ncbi.nlm.nih.gov/pubmed/30872918
http://dx.doi.org/10.1177/1176934319831308
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author Morton, Scott P
Phillips, Julie B
Phillips, Joshua L
author_facet Morton, Scott P
Phillips, Julie B
Phillips, Joshua L
author_sort Morton, Scott P
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description Decades of research has yet to provide a vaccine for HIV, the virus which causes AIDS. Recent theoretical research has turned attention to mucosa pH levels over systemic pH levels. Previous research in this field developed a computational approach for determining pH sensitivity that indicated higher potential for transmission at mucosa pH levels present during intercourse. The process was extended to incorporate a principal component analysis (PCA)-based machine learning technique for classification of gp120 proteins against a known transmitted variant called Biomolecular Electro-Static Indexing (BESI). The original process has since been extended to the residue level by a process we termed Electrostatic Variance Masking (EVM) and used in conjunction with BESI to determine structural differences present among various subspecies across Clades A1 and C. Results indicate that structures outside of the core selected by EVM may be responsible for binding affinity observed in many other studies and that pH modulation of select substructures indicated by EVM may influence specific regions of the viral envelope protein (Env) involved in protein-protein interactions.
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spelling pubmed-64071672019-03-14 The Molecular Basis of pH-Modulated HIV gp120 Binding Revealed Morton, Scott P Phillips, Julie B Phillips, Joshua L Evol Bioinform Online Original Research Decades of research has yet to provide a vaccine for HIV, the virus which causes AIDS. Recent theoretical research has turned attention to mucosa pH levels over systemic pH levels. Previous research in this field developed a computational approach for determining pH sensitivity that indicated higher potential for transmission at mucosa pH levels present during intercourse. The process was extended to incorporate a principal component analysis (PCA)-based machine learning technique for classification of gp120 proteins against a known transmitted variant called Biomolecular Electro-Static Indexing (BESI). The original process has since been extended to the residue level by a process we termed Electrostatic Variance Masking (EVM) and used in conjunction with BESI to determine structural differences present among various subspecies across Clades A1 and C. Results indicate that structures outside of the core selected by EVM may be responsible for binding affinity observed in many other studies and that pH modulation of select substructures indicated by EVM may influence specific regions of the viral envelope protein (Env) involved in protein-protein interactions. SAGE Publications 2019-03-07 /pmc/articles/PMC6407167/ /pubmed/30872918 http://dx.doi.org/10.1177/1176934319831308 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Morton, Scott P
Phillips, Julie B
Phillips, Joshua L
The Molecular Basis of pH-Modulated HIV gp120 Binding Revealed
title The Molecular Basis of pH-Modulated HIV gp120 Binding Revealed
title_full The Molecular Basis of pH-Modulated HIV gp120 Binding Revealed
title_fullStr The Molecular Basis of pH-Modulated HIV gp120 Binding Revealed
title_full_unstemmed The Molecular Basis of pH-Modulated HIV gp120 Binding Revealed
title_short The Molecular Basis of pH-Modulated HIV gp120 Binding Revealed
title_sort molecular basis of ph-modulated hiv gp120 binding revealed
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407167/
https://www.ncbi.nlm.nih.gov/pubmed/30872918
http://dx.doi.org/10.1177/1176934319831308
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