Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)

ABSTRACT Objective: This study focused on purifying and characterizing a lectin from Lepechinia bullata (L. bullata) seeds, and determining its specificity towards tumour-associated carbohydrate-antigens. Methods: Pigments were removed by washing the seeds with NH4OH 0.1 M pH 9.4 and treating the cr...

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Autores:
Wilches Torres, Andrea
Rojas Caraballo, José Vicente
Sanabria, Edilma
Reyes Montaño, Edgar
Fernández Alonso, Jose Luis
Varrot, Annabelle
Imberty, Anne
Vega, Nohora
Tipo de recurso:
Article of journal
Fecha de publicación:
2017
Institución:
Universidad Cooperativa de Colombia
Repositorio:
Repositorio UCC
Idioma:
OAI Identifier:
oai:repository.ucc.edu.co:20.500.12494/4295
Acceso en línea:
https://hdl.handle.net/20.500.12494/4295
Palabra clave:
lamiaceae lectin
lepechinia bullata
Protein
Purification
Rights
openAccess
License
Licencia CC
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oai_identifier_str oai:repository.ucc.edu.co:20.500.12494/4295
network_acronym_str COOPER2
network_name_str Repositorio UCC
repository_id_str
dc.title.spa.fl_str_mv Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)
title Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)
spellingShingle Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)
lamiaceae lectin
lepechinia bullata
Protein
Purification
title_short Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)
title_full Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)
title_fullStr Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)
title_full_unstemmed Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)
title_sort Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)
dc.creator.fl_str_mv Wilches Torres, Andrea
Rojas Caraballo, José Vicente
Sanabria, Edilma
Reyes Montaño, Edgar
Fernández Alonso, Jose Luis
Varrot, Annabelle
Imberty, Anne
Vega, Nohora
dc.contributor.author.none.fl_str_mv Wilches Torres, Andrea
Rojas Caraballo, José Vicente
Sanabria, Edilma
Reyes Montaño, Edgar
Fernández Alonso, Jose Luis
Varrot, Annabelle
Imberty, Anne
Vega, Nohora
dc.subject.spa.fl_str_mv lamiaceae lectin
lepechinia bullata
Protein
Purification
topic lamiaceae lectin
lepechinia bullata
Protein
Purification
description ABSTRACT Objective: This study focused on purifying and characterizing a lectin from Lepechinia bullata (L. bullata) seeds, and determining its specificity towards tumour-associated carbohydrate-antigens. Methods: Pigments were removed by washing the seeds with NH4OH 0.1 M pH 9.4 and treating the crude extracts with Pectinex®. The purification procedure consisted of anion exchange chromatography on diethylaminoethyl (DEAE)-Sephadex followed by affinity chromatography. For the characterization, the phase was used polyacrylamide gel electrophoresis-sodium dodecyl sulphate (SDS-PAGE), isoelectric focusing, hemagglutination assays, enzyme-linked lectinosorbent assay (ELLA) and thermal shift assay (TSA). Results: 6.2 mg of lectin were obtained from 100 g of seeds. It was able to agglutinate enzymatically treated erythrocytes with a minimal required lectin concentration of 7 μg. ml-1. Strong binding to asialo bovine submaxillary mucine (aBSM) was determined, corroborating Tn recognition. The isoelectric focusing showed a unique band at pH 8.5. Lectin pure shown bands at 28, 48 and 93 kDa by SDS-PAGE, with an incomplete dissociation of the last species despite trying several reduction conditions. By preparative electrophoresis under different conditions, three species were observed too, in all fractions one band at 28 kDa on Tricine-PAGE in reducing and no reducing conditions were found. Amino acid composition, carbohydrate content, thermal stability and Ca2+and Mn2+requirements were determined. N-acetylgalactosamine (GalNAc) and desialylated mucins inhibited the agglutinant activity on human cells. Fetuin inhibited hemagglutination of rabbit erythrocytes. Conclusion: A new lectin was isolated and characterized from L. bullata seeds, it recognizes T/Tn antigen and shows some similarities with other Lamiaceae lectins.
publishDate 2017
dc.date.issued.none.fl_str_mv 2017-09-21
dc.date.accessioned.none.fl_str_mv 2018-06-13T20:16:03Z
dc.date.available.none.fl_str_mv 2018-06-13T20:16:03Z
dc.type.none.fl_str_mv Artículo
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
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dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/20.500.12494/4295
dc.identifier.bibliographicCitation.spa.fl_str_mv Wilches Torres, A., Rojas Caraballo, J., Sanabria, E., Reyes Montaño, E., Fernández Alonso, J. L., Varrot, A., Imberty, A., y Vega, N. (2017). Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE). International Journal of Pharmacy and Pharmaceutical Sciences , 9(11), 165-174.
url https://hdl.handle.net/20.500.12494/4295
identifier_str_mv Wilches Torres, A., Rojas Caraballo, J., Sanabria, E., Reyes Montaño, E., Fernández Alonso, J. L., Varrot, A., Imberty, A., y Vega, N. (2017). Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE). International Journal of Pharmacy and Pharmaceutical Sciences , 9(11), 165-174.
dc.rights.cc.none.fl_str_mv Licencia CC
dc.rights.accessrights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.coar.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
rights_invalid_str_mv Licencia CC
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.publisher.spa.fl_str_mv Universidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Medicina, Santa Marta
dc.publisher.program.spa.fl_str_mv Medicina
dc.publisher.place.spa.fl_str_mv Santa Marta
institution Universidad Cooperativa de Colombia
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spelling Wilches Torres, AndreaRojas Caraballo, José VicenteSanabria, EdilmaReyes Montaño, EdgarFernández Alonso, Jose LuisVarrot, AnnabelleImberty, AnneVega, Nohora2018-06-13T20:16:03Z2018-06-13T20:16:03Z2017-09-21https://hdl.handle.net/20.500.12494/4295Wilches Torres, A., Rojas Caraballo, J., Sanabria, E., Reyes Montaño, E., Fernández Alonso, J. L., Varrot, A., Imberty, A., y Vega, N. (2017). Purification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE). International Journal of Pharmacy and Pharmaceutical Sciences , 9(11), 165-174.ABSTRACT Objective: This study focused on purifying and characterizing a lectin from Lepechinia bullata (L. bullata) seeds, and determining its specificity towards tumour-associated carbohydrate-antigens. Methods: Pigments were removed by washing the seeds with NH4OH 0.1 M pH 9.4 and treating the crude extracts with Pectinex®. The purification procedure consisted of anion exchange chromatography on diethylaminoethyl (DEAE)-Sephadex followed by affinity chromatography. For the characterization, the phase was used polyacrylamide gel electrophoresis-sodium dodecyl sulphate (SDS-PAGE), isoelectric focusing, hemagglutination assays, enzyme-linked lectinosorbent assay (ELLA) and thermal shift assay (TSA). Results: 6.2 mg of lectin were obtained from 100 g of seeds. It was able to agglutinate enzymatically treated erythrocytes with a minimal required lectin concentration of 7 μg. ml-1. Strong binding to asialo bovine submaxillary mucine (aBSM) was determined, corroborating Tn recognition. The isoelectric focusing showed a unique band at pH 8.5. Lectin pure shown bands at 28, 48 and 93 kDa by SDS-PAGE, with an incomplete dissociation of the last species despite trying several reduction conditions. By preparative electrophoresis under different conditions, three species were observed too, in all fractions one band at 28 kDa on Tricine-PAGE in reducing and no reducing conditions were found. Amino acid composition, carbohydrate content, thermal stability and Ca2+and Mn2+requirements were determined. N-acetylgalactosamine (GalNAc) and desialylated mucins inhibited the agglutinant activity on human cells. Fetuin inhibited hemagglutination of rabbit erythrocytes. Conclusion: A new lectin was isolated and characterized from L. bullata seeds, it recognizes T/Tn antigen and shows some similarities with other Lamiaceae lectins.josev.rojas@campusucc.edu.coUniversidad Cooperativa de Colombia, Facultad de Ciencias de la Salud, Medicina, Santa MartaMedicinaSanta Martalamiaceae lectinlepechinia bullataProteinPurificationPurification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds (LAMIACEAE)Artículohttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1http://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionLicencia CCinfo:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2PublicationORIGINALP2.pdfP2.pdfPurification and biochemical characterization of a t/tn specific lectin from lepechinia bullata seeds 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