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...
- 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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| 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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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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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 |
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1 |
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11 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Toxins |
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14 páginas |
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application/pdf |
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MDPI (Multidisciplinary Digital Publishing Institute) |
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Basilea, Suiza |
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Universidad de Antioquia |
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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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