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Recombinant expression and antigenicity of two peptide families of neurotoxins from Androctonus sp.
BACKGROUND: Scorpion neurotoxins such as those that modify the mammalian voltage-gated sodium ion channels (Nav) are the main responsible for scorpion envenomation. Their neutralization is crucial in the production of antivenoms against scorpion stings. METHODS: In the present study, two in silico d...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP)
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769139/ https://www.ncbi.nlm.nih.gov/pubmed/36578820 http://dx.doi.org/10.1590/1678-9199-JVATITD-2022-0026 |
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author | Cardoso-Arenas, Samuel Clement, Herlinda Arenas, Iván Olvera, Felipe Zamudio, Fernando Caliskan, Figen Corrales-García, Ligia Luz Corzo, Gerardo |
author_facet | Cardoso-Arenas, Samuel Clement, Herlinda Arenas, Iván Olvera, Felipe Zamudio, Fernando Caliskan, Figen Corrales-García, Ligia Luz Corzo, Gerardo |
author_sort | Cardoso-Arenas, Samuel |
collection | PubMed |
description | BACKGROUND: Scorpion neurotoxins such as those that modify the mammalian voltage-gated sodium ion channels (Nav) are the main responsible for scorpion envenomation. Their neutralization is crucial in the production of antivenoms against scorpion stings. METHODS: In the present study, two in silico designed genes - one that codes for a native neurotoxin from the venom of the Anatolian scorpion Androctonus crassicauda, named Acra 4 - and another non-native toxin - named consensus scorpion toxin (SccTx) obtained from the alignment of the primary structures of the most toxic neurotoxins from the Middle Eastern and North African scorpions - were recombinantly expressed in E. coli Origami. RESULTS: Following bacterial expression, the two expressed neurotoxins, hereafter named HisrAcra4 and HisrSccTx, were obtained from inclusion bodies. Both recombinant neurotoxins were obtained in multiple Cys-Cys isoforms. After refolding, the active protein fractions were identified with molecular masses of 8,947.6 and 9,989.1 Da for HisrAcra4 and HisrSccTx, respectively, which agreed with their expected theoretical masses. HisrAcra4 and HisrSccTx were used as antigens to immunize two groups of rabbits, to produce either anti-HisrAcra4 or anti-HisrSccTx serum antibodies, which in turn could recognize and neutralize neurotoxins from venoms of scorpion species from the Middle East and North Africa. The antibodies obtained from rabbits neutralized the 3LD(50) of Androctonus australis, Leiurus quinquestriatus hebraeus and Buthus occitanus venoms, but they did not neutralize A. crassicauda and A. mauritanicus venoms. In addition, the anti-HisrAcra4 antibodies did not neutralize any of the five scorpion venoms tested. However, an antibody blend of anti-HisrAcra4 and anti-HisrSccTx was able to neutralize A. crassicauda and A. mauritanicus venoms. CONCLUSIONS: Two recombinant Nav neurotoxins, from different peptide families, were used as antigens to generate IgGs for neutralizing scorpion venoms of species from the Middle East and North Africa. |
format | Online Article Text |
id | pubmed-9769139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP) |
record_format | MEDLINE/PubMed |
spelling | pubmed-97691392022-12-27 Recombinant expression and antigenicity of two peptide families of neurotoxins from Androctonus sp. Cardoso-Arenas, Samuel Clement, Herlinda Arenas, Iván Olvera, Felipe Zamudio, Fernando Caliskan, Figen Corrales-García, Ligia Luz Corzo, Gerardo J Venom Anim Toxins Incl Trop Dis Research BACKGROUND: Scorpion neurotoxins such as those that modify the mammalian voltage-gated sodium ion channels (Nav) are the main responsible for scorpion envenomation. Their neutralization is crucial in the production of antivenoms against scorpion stings. METHODS: In the present study, two in silico designed genes - one that codes for a native neurotoxin from the venom of the Anatolian scorpion Androctonus crassicauda, named Acra 4 - and another non-native toxin - named consensus scorpion toxin (SccTx) obtained from the alignment of the primary structures of the most toxic neurotoxins from the Middle Eastern and North African scorpions - were recombinantly expressed in E. coli Origami. RESULTS: Following bacterial expression, the two expressed neurotoxins, hereafter named HisrAcra4 and HisrSccTx, were obtained from inclusion bodies. Both recombinant neurotoxins were obtained in multiple Cys-Cys isoforms. After refolding, the active protein fractions were identified with molecular masses of 8,947.6 and 9,989.1 Da for HisrAcra4 and HisrSccTx, respectively, which agreed with their expected theoretical masses. HisrAcra4 and HisrSccTx were used as antigens to immunize two groups of rabbits, to produce either anti-HisrAcra4 or anti-HisrSccTx serum antibodies, which in turn could recognize and neutralize neurotoxins from venoms of scorpion species from the Middle East and North Africa. The antibodies obtained from rabbits neutralized the 3LD(50) of Androctonus australis, Leiurus quinquestriatus hebraeus and Buthus occitanus venoms, but they did not neutralize A. crassicauda and A. mauritanicus venoms. In addition, the anti-HisrAcra4 antibodies did not neutralize any of the five scorpion venoms tested. However, an antibody blend of anti-HisrAcra4 and anti-HisrSccTx was able to neutralize A. crassicauda and A. mauritanicus venoms. CONCLUSIONS: Two recombinant Nav neurotoxins, from different peptide families, were used as antigens to generate IgGs for neutralizing scorpion venoms of species from the Middle East and North Africa. Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP) 2022-12-19 /pmc/articles/PMC9769139/ /pubmed/36578820 http://dx.doi.org/10.1590/1678-9199-JVATITD-2022-0026 Text en https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Cardoso-Arenas, Samuel Clement, Herlinda Arenas, Iván Olvera, Felipe Zamudio, Fernando Caliskan, Figen Corrales-García, Ligia Luz Corzo, Gerardo Recombinant expression and antigenicity of two peptide families of neurotoxins from Androctonus sp. |
title | Recombinant expression and antigenicity of two peptide families of neurotoxins from Androctonus sp. |
title_full | Recombinant expression and antigenicity of two peptide families of neurotoxins from Androctonus sp. |
title_fullStr | Recombinant expression and antigenicity of two peptide families of neurotoxins from Androctonus sp. |
title_full_unstemmed | Recombinant expression and antigenicity of two peptide families of neurotoxins from Androctonus sp. |
title_short | Recombinant expression and antigenicity of two peptide families of neurotoxins from Androctonus sp. |
title_sort | recombinant expression and antigenicity of two peptide families of neurotoxins from androctonus sp. |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769139/ https://www.ncbi.nlm.nih.gov/pubmed/36578820 http://dx.doi.org/10.1590/1678-9199-JVATITD-2022-0026 |
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