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An immunoinformatic approach to assessing the immunogenic capacity of alpha-neurotoxins in elapid snake venoms
Introduction: Most elapid snakes produce venoms that contain alpha-neurotoxins (α-NTXs), which are proteins that cause post-synaptic blockade and paralysis in snakebite envenoming. However, existing elapid antivenoms are known for their low potency in neutralizing the neurotoxic activity of α-NTXs,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155835/ https://www.ncbi.nlm.nih.gov/pubmed/37153801 http://dx.doi.org/10.3389/fphar.2023.1143437 |
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author | Chan, Yi Wei Tan, Choo Hock Heh, Choon Han Tan, Kae Yi |
author_facet | Chan, Yi Wei Tan, Choo Hock Heh, Choon Han Tan, Kae Yi |
author_sort | Chan, Yi Wei |
collection | PubMed |
description | Introduction: Most elapid snakes produce venoms that contain alpha-neurotoxins (α-NTXs), which are proteins that cause post-synaptic blockade and paralysis in snakebite envenoming. However, existing elapid antivenoms are known for their low potency in neutralizing the neurotoxic activity of α-NTXs, while the immunological basis has not been elucidated. Methods: In this study, a structure-based major histocompatibility complex II (MHCII) epitope predictor of horse (Equus caballus), complemented with DM-editing determinant screening algorithm was adopted to assess the immunogenicity of α-NTXs in the venoms of major Asiatic elapids (Naja kaouthia, Ophiophagus hannah, Laticauda colubrina, Hydrophis schistosus, Hydrophis curtus). Results: The scoring metric M(2)R, representing the relative immunogenic performance of respective α-NTXs, showed all α-NTXs have an overall low M(2)R of <0.3, and most of the predicted binders feature non-optimal P1 anchor residues. The M(2)R scores correlate strongly (R(2) = 0.82) with the potency scores (p-score) generated based on the relative abundances of α-NTXs and the neutralization potency of commercial antivenoms. Discussion: The immunoinformatic analysis indicates that the inferior antigenicity of α-NTXs is not only due to their small molecular size but also the subpar immunogenicity affected by their amino acid composition. Structural modification with conjugation and synthetic epitope as immunogen may potentially enhance the immunogenicity for improved antivenom potency against α-NTXs of elapid snakes. |
format | Online Article Text |
id | pubmed-10155835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101558352023-05-04 An immunoinformatic approach to assessing the immunogenic capacity of alpha-neurotoxins in elapid snake venoms Chan, Yi Wei Tan, Choo Hock Heh, Choon Han Tan, Kae Yi Front Pharmacol Pharmacology Introduction: Most elapid snakes produce venoms that contain alpha-neurotoxins (α-NTXs), which are proteins that cause post-synaptic blockade and paralysis in snakebite envenoming. However, existing elapid antivenoms are known for their low potency in neutralizing the neurotoxic activity of α-NTXs, while the immunological basis has not been elucidated. Methods: In this study, a structure-based major histocompatibility complex II (MHCII) epitope predictor of horse (Equus caballus), complemented with DM-editing determinant screening algorithm was adopted to assess the immunogenicity of α-NTXs in the venoms of major Asiatic elapids (Naja kaouthia, Ophiophagus hannah, Laticauda colubrina, Hydrophis schistosus, Hydrophis curtus). Results: The scoring metric M(2)R, representing the relative immunogenic performance of respective α-NTXs, showed all α-NTXs have an overall low M(2)R of <0.3, and most of the predicted binders feature non-optimal P1 anchor residues. The M(2)R scores correlate strongly (R(2) = 0.82) with the potency scores (p-score) generated based on the relative abundances of α-NTXs and the neutralization potency of commercial antivenoms. Discussion: The immunoinformatic analysis indicates that the inferior antigenicity of α-NTXs is not only due to their small molecular size but also the subpar immunogenicity affected by their amino acid composition. Structural modification with conjugation and synthetic epitope as immunogen may potentially enhance the immunogenicity for improved antivenom potency against α-NTXs of elapid snakes. Frontiers Media S.A. 2023-04-10 /pmc/articles/PMC10155835/ /pubmed/37153801 http://dx.doi.org/10.3389/fphar.2023.1143437 Text en Copyright © 2023 Chan, Tan, Heh and Tan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Chan, Yi Wei Tan, Choo Hock Heh, Choon Han Tan, Kae Yi An immunoinformatic approach to assessing the immunogenic capacity of alpha-neurotoxins in elapid snake venoms |
title | An immunoinformatic approach to assessing the immunogenic capacity of alpha-neurotoxins in elapid snake venoms |
title_full | An immunoinformatic approach to assessing the immunogenic capacity of alpha-neurotoxins in elapid snake venoms |
title_fullStr | An immunoinformatic approach to assessing the immunogenic capacity of alpha-neurotoxins in elapid snake venoms |
title_full_unstemmed | An immunoinformatic approach to assessing the immunogenic capacity of alpha-neurotoxins in elapid snake venoms |
title_short | An immunoinformatic approach to assessing the immunogenic capacity of alpha-neurotoxins in elapid snake venoms |
title_sort | immunoinformatic approach to assessing the immunogenic capacity of alpha-neurotoxins in elapid snake venoms |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10155835/ https://www.ncbi.nlm.nih.gov/pubmed/37153801 http://dx.doi.org/10.3389/fphar.2023.1143437 |
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