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A detection and quantification label-free tool to speed up downstream processing of model mucins

Mucins are high-molecular weight glycoproteins (0.25–20 MDa) containing one or more domains that are heavily O-glycosylated. Their implications as targets for cancer treatment have increased the interest in these glycoproteins, mainly in the fields of vaccines and antibodies. However, mucins present...

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Autores principales: Carvalho, Sofia B., Moreira, Ana Sofia, Gomes, Joana, Carrondo, Manuel J. T., Thornton, David J., Alves, Paula M., Costa, Julia, Peixoto, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760085/
https://www.ncbi.nlm.nih.gov/pubmed/29315346
http://dx.doi.org/10.1371/journal.pone.0190974
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author Carvalho, Sofia B.
Moreira, Ana Sofia
Gomes, Joana
Carrondo, Manuel J. T.
Thornton, David J.
Alves, Paula M.
Costa, Julia
Peixoto, Cristina
author_facet Carvalho, Sofia B.
Moreira, Ana Sofia
Gomes, Joana
Carrondo, Manuel J. T.
Thornton, David J.
Alves, Paula M.
Costa, Julia
Peixoto, Cristina
author_sort Carvalho, Sofia B.
collection PubMed
description Mucins are high-molecular weight glycoproteins (0.25–20 MDa) containing one or more domains that are heavily O-glycosylated. Their implications as targets for cancer treatment have increased the interest in these glycoproteins, mainly in the fields of vaccines and antibodies. However, mucins present high heterogeneity, posing challenges that affect purification processes and quality control analysis. In that sense, it is necessary to develop and improve downstream processes and analytical methods to characterize these products. Here a tool based on biolayer interferometry analysis to improve mucin’s detection and quantification in a fast, simple and label free-way is presented. Taking advantage of lectin recognition of mucins’ carbohydrate structures, several lectins were evaluated and immobilized on streptavidin biosensors. Different assay conditions were optimized and the most suitable lectin, Aleuria aurantia lectin (AAL), was selected. Bovine Submaxillary Gland and human MUC5B mucins were used as proof of concept and were successfully detected and quantified at different stages of purification. High sensitivity levels were achieved with LOD and LOQ of 3.8 μg mL(-1) and 11.7 μg mL(-1) for BSM, and 0.2 μg mL(-1) and 0.6 μg mL(-1) for MUC5B. AAL binding specificity was also confirmed with fucose competition assays. Our method represents an advance on mucins detection and quantification since the existing methods present several disadvantages for process development. Hereafter, it can be applied to the optimization of new or already established downstream processes for mucins’ purification.
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spelling pubmed-57600852018-01-22 A detection and quantification label-free tool to speed up downstream processing of model mucins Carvalho, Sofia B. Moreira, Ana Sofia Gomes, Joana Carrondo, Manuel J. T. Thornton, David J. Alves, Paula M. Costa, Julia Peixoto, Cristina PLoS One Research Article Mucins are high-molecular weight glycoproteins (0.25–20 MDa) containing one or more domains that are heavily O-glycosylated. Their implications as targets for cancer treatment have increased the interest in these glycoproteins, mainly in the fields of vaccines and antibodies. However, mucins present high heterogeneity, posing challenges that affect purification processes and quality control analysis. In that sense, it is necessary to develop and improve downstream processes and analytical methods to characterize these products. Here a tool based on biolayer interferometry analysis to improve mucin’s detection and quantification in a fast, simple and label free-way is presented. Taking advantage of lectin recognition of mucins’ carbohydrate structures, several lectins were evaluated and immobilized on streptavidin biosensors. Different assay conditions were optimized and the most suitable lectin, Aleuria aurantia lectin (AAL), was selected. Bovine Submaxillary Gland and human MUC5B mucins were used as proof of concept and were successfully detected and quantified at different stages of purification. High sensitivity levels were achieved with LOD and LOQ of 3.8 μg mL(-1) and 11.7 μg mL(-1) for BSM, and 0.2 μg mL(-1) and 0.6 μg mL(-1) for MUC5B. AAL binding specificity was also confirmed with fucose competition assays. Our method represents an advance on mucins detection and quantification since the existing methods present several disadvantages for process development. Hereafter, it can be applied to the optimization of new or already established downstream processes for mucins’ purification. Public Library of Science 2018-01-09 /pmc/articles/PMC5760085/ /pubmed/29315346 http://dx.doi.org/10.1371/journal.pone.0190974 Text en © 2018 Carvalho et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Carvalho, Sofia B.
Moreira, Ana Sofia
Gomes, Joana
Carrondo, Manuel J. T.
Thornton, David J.
Alves, Paula M.
Costa, Julia
Peixoto, Cristina
A detection and quantification label-free tool to speed up downstream processing of model mucins
title A detection and quantification label-free tool to speed up downstream processing of model mucins
title_full A detection and quantification label-free tool to speed up downstream processing of model mucins
title_fullStr A detection and quantification label-free tool to speed up downstream processing of model mucins
title_full_unstemmed A detection and quantification label-free tool to speed up downstream processing of model mucins
title_short A detection and quantification label-free tool to speed up downstream processing of model mucins
title_sort detection and quantification label-free tool to speed up downstream processing of model mucins
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760085/
https://www.ncbi.nlm.nih.gov/pubmed/29315346
http://dx.doi.org/10.1371/journal.pone.0190974
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