Immunogenic properties of recombinant enzymes from bothrops ammodytoides towards the generation of neutralizing antibodies against its own venom

ABSTRACT: Bothropic venoms contain enzymes such as metalloproteases, serine-proteases, and phospholipases, which acting by themselves, or in synergism, are the cause of the envenomation symptoms and death. Here, two mRNA transcripts, one that codes for a metalloprotease and another for a serine-prot...

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Autores:
Corrales García, Ligia Luz
Clement, Herlinda
Bolaños, Damaris
Corzo, Gerardo
Villegas, Elba
Tipo de recurso:
Article of investigation
Fecha de publicación:
2019
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/38234
Acceso en línea:
https://hdl.handle.net/10495/38234
Palabra clave:
Bothrops
Anticuerpos Neutralizantes - inmunología
Antibodies, Neutralizing - immunology
Venenos de Crotálidos - química
Crotalid Venoms - chemistry
Venenos de Crotálidos - inmunología
Crotalid Venoms - immunology
Metaloproteasas
Metalloproteases
Fosfolipasas
Phospholipases
Conejos
Rabbits
Proteínas Recombinantes
Recombinant Proteins
Proteínas de Reptiles
Reptilian Proteins
Serina Proteasas
Serine Proteases
https://id.nlm.nih.gov/mesh/D017837
https://id.nlm.nih.gov/mesh/D057134
https://id.nlm.nih.gov/mesh/D003435
https://id.nlm.nih.gov/mesh/D045726
https://id.nlm.nih.gov/mesh/D010740
https://id.nlm.nih.gov/mesh/D011817
https://id.nlm.nih.gov/mesh/D030162
https://id.nlm.nih.gov/mesh/D057057
Rights
openAccess
License
https://creativecommons.org/licenses/by/4.0/
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oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/38234
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Immunogenic properties of recombinant enzymes from bothrops ammodytoides towards the generation of neutralizing antibodies against its own venom
title Immunogenic properties of recombinant enzymes from bothrops ammodytoides towards the generation of neutralizing antibodies against its own venom
spellingShingle Immunogenic properties of recombinant enzymes from bothrops ammodytoides towards the generation of neutralizing antibodies against its own venom
Bothrops
Anticuerpos Neutralizantes - inmunología
Antibodies, Neutralizing - immunology
Venenos de Crotálidos - química
Crotalid Venoms - chemistry
Venenos de Crotálidos - inmunología
Crotalid Venoms - immunology
Metaloproteasas
Metalloproteases
Fosfolipasas
Phospholipases
Conejos
Rabbits
Proteínas Recombinantes
Recombinant Proteins
Proteínas de Reptiles
Reptilian Proteins
Serina Proteasas
Serine Proteases
https://id.nlm.nih.gov/mesh/D017837
https://id.nlm.nih.gov/mesh/D057134
https://id.nlm.nih.gov/mesh/D003435
https://id.nlm.nih.gov/mesh/D045726
https://id.nlm.nih.gov/mesh/D010740
https://id.nlm.nih.gov/mesh/D011817
https://id.nlm.nih.gov/mesh/D030162
https://id.nlm.nih.gov/mesh/D057057
title_short Immunogenic properties of recombinant enzymes from bothrops ammodytoides towards the generation of neutralizing antibodies against its own venom
title_full Immunogenic properties of recombinant enzymes from bothrops ammodytoides towards the generation of neutralizing antibodies against its own venom
title_fullStr Immunogenic properties of recombinant enzymes from bothrops ammodytoides towards the generation of neutralizing antibodies against its own venom
title_full_unstemmed Immunogenic properties of recombinant enzymes from bothrops ammodytoides towards the generation of neutralizing antibodies against its own venom
title_sort Immunogenic properties of recombinant enzymes from bothrops ammodytoides towards the generation of neutralizing antibodies against its own venom
dc.creator.fl_str_mv Corrales García, Ligia Luz
Clement, Herlinda
Bolaños, Damaris
Corzo, Gerardo
Villegas, Elba
dc.contributor.author.none.fl_str_mv Corrales García, Ligia Luz
Clement, Herlinda
Bolaños, Damaris
Corzo, Gerardo
Villegas, Elba
dc.contributor.researchgroup.spa.fl_str_mv Diseño y Formulación de Medicamentos Cosméticos y Afines
dc.subject.decs.none.fl_str_mv Bothrops
Anticuerpos Neutralizantes - inmunología
Antibodies, Neutralizing - immunology
Venenos de Crotálidos - química
Crotalid Venoms - chemistry
Venenos de Crotálidos - inmunología
Crotalid Venoms - immunology
Metaloproteasas
Metalloproteases
Fosfolipasas
Phospholipases
Conejos
Rabbits
Proteínas Recombinantes
Recombinant Proteins
Proteínas de Reptiles
Reptilian Proteins
Serina Proteasas
Serine Proteases
topic Bothrops
Anticuerpos Neutralizantes - inmunología
Antibodies, Neutralizing - immunology
Venenos de Crotálidos - química
Crotalid Venoms - chemistry
Venenos de Crotálidos - inmunología
Crotalid Venoms - immunology
Metaloproteasas
Metalloproteases
Fosfolipasas
Phospholipases
Conejos
Rabbits
Proteínas Recombinantes
Recombinant Proteins
Proteínas de Reptiles
Reptilian Proteins
Serina Proteasas
Serine Proteases
https://id.nlm.nih.gov/mesh/D017837
https://id.nlm.nih.gov/mesh/D057134
https://id.nlm.nih.gov/mesh/D003435
https://id.nlm.nih.gov/mesh/D045726
https://id.nlm.nih.gov/mesh/D010740
https://id.nlm.nih.gov/mesh/D011817
https://id.nlm.nih.gov/mesh/D030162
https://id.nlm.nih.gov/mesh/D057057
dc.subject.meshuri.none.fl_str_mv https://id.nlm.nih.gov/mesh/D017837
https://id.nlm.nih.gov/mesh/D057134
https://id.nlm.nih.gov/mesh/D003435
https://id.nlm.nih.gov/mesh/D045726
https://id.nlm.nih.gov/mesh/D010740
https://id.nlm.nih.gov/mesh/D011817
https://id.nlm.nih.gov/mesh/D030162
https://id.nlm.nih.gov/mesh/D057057
description ABSTRACT: Bothropic venoms contain enzymes such as metalloproteases, serine-proteases, and phospholipases, which acting by themselves, or in synergism, are the cause of the envenomation symptoms and death. Here, two mRNA transcripts, one that codes for a metalloprotease and another for a serine-protease, were isolated from a Bothrops ammodytoides venom gland. The metalloprotease and serine-protease transcripts were cloned on a pCR®2.1-TOPO vector and consequently expressed in a recombinant way in E. coli (strains Origami and M15, respectively), using pQE30 vectors. The recombinant proteins were named rBamSP_1 and rBamMP_1, and they were formed by an N-terminal fusion protein of 16 amino acid residues, followed by the sequence of the mature proteins. After bacterial expression, each recombinant enzyme was recovered from inclusion bodies and treated with chaotropic agents. The experimental molecular masses for rBamSP_1 and rBamMP_1 agreed with their expected theoretical ones, and their secondary structure spectra obtained by circular dichroism were comparable to that of similar proteins. Additionally, equivalent mixtures of rBamSP_1, rBamMP_1 together with a previous reported recombinant phospholipase, rBamPLA2_1, were used to immunize rabbits to produce serum antibodies, which in turn recognized serine-proteases, metalloproteases and PLA2s from B. ammodytoides and other regional viper venoms. Finally, rabbit antibodies neutralized the 3LD50 of B. ammodytoides venom.
publishDate 2019
dc.date.issued.none.fl_str_mv 2019
dc.date.accessioned.none.fl_str_mv 2024-02-19T23:42:05Z
dc.date.available.none.fl_str_mv 2024-02-19T23:42:05Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/38234
dc.identifier.doi.none.fl_str_mv 10.3390/toxins11120702
dc.identifier.eissn.none.fl_str_mv 2072-6652
url https://hdl.handle.net/10495/38234
identifier_str_mv 10.3390/toxins11120702
2072-6652
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Toxins
dc.relation.citationendpage.spa.fl_str_mv 14
dc.relation.citationissue.spa.fl_str_mv 12
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 11
dc.relation.ispartofjournal.spa.fl_str_mv Toxins
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institution Universidad de Antioquia
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spelling Corrales García, Ligia LuzClement, HerlindaBolaños, DamarisCorzo, GerardoVillegas, ElbaDiseño y Formulación de Medicamentos Cosméticos y Afines2024-02-19T23:42:05Z2024-02-19T23:42:05Z2019https://hdl.handle.net/10495/3823410.3390/toxins111207022072-6652ABSTRACT: Bothropic venoms contain enzymes such as metalloproteases, serine-proteases, and phospholipases, which acting by themselves, or in synergism, are the cause of the envenomation symptoms and death. Here, two mRNA transcripts, one that codes for a metalloprotease and another for a serine-protease, were isolated from a Bothrops ammodytoides venom gland. The metalloprotease and serine-protease transcripts were cloned on a pCR®2.1-TOPO vector and consequently expressed in a recombinant way in E. coli (strains Origami and M15, respectively), using pQE30 vectors. The recombinant proteins were named rBamSP_1 and rBamMP_1, and they were formed by an N-terminal fusion protein of 16 amino acid residues, followed by the sequence of the mature proteins. After bacterial expression, each recombinant enzyme was recovered from inclusion bodies and treated with chaotropic agents. The experimental molecular masses for rBamSP_1 and rBamMP_1 agreed with their expected theoretical ones, and their secondary structure spectra obtained by circular dichroism were comparable to that of similar proteins. Additionally, equivalent mixtures of rBamSP_1, rBamMP_1 together with a previous reported recombinant phospholipase, rBamPLA2_1, were used to immunize rabbits to produce serum antibodies, which in turn recognized serine-proteases, metalloproteases and PLA2s from B. ammodytoides and other regional viper venoms. 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