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Methodologies to generate, extract, purify and fractionate yeast ECM for analytical use in proteomics and glycomics

BACKGROUND: In a multicellular organism, the extracellular matrix (ECM) provides a cell-supporting scaffold and helps maintaining the biophysical integrity of tissues and organs. At the same time it plays crucial roles in cellular communication and signalling, with implications in spatial organisati...

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Autores principales: Faria-Oliveira, Fábio, Carvalho, Joana, Belmiro, Celso LR, Martinez-Gomariz, Montserrat, Hernaez, Maria Luisa, Pavão, Mauro, Gil, Concha, Lucas, Cândida, Ferreira, Célia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219020/
https://www.ncbi.nlm.nih.gov/pubmed/25344425
http://dx.doi.org/10.1186/s12866-014-0244-0
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author Faria-Oliveira, Fábio
Carvalho, Joana
Belmiro, Celso LR
Martinez-Gomariz, Montserrat
Hernaez, Maria Luisa
Pavão, Mauro
Gil, Concha
Lucas, Cândida
Ferreira, Célia
author_facet Faria-Oliveira, Fábio
Carvalho, Joana
Belmiro, Celso LR
Martinez-Gomariz, Montserrat
Hernaez, Maria Luisa
Pavão, Mauro
Gil, Concha
Lucas, Cândida
Ferreira, Célia
author_sort Faria-Oliveira, Fábio
collection PubMed
description BACKGROUND: In a multicellular organism, the extracellular matrix (ECM) provides a cell-supporting scaffold and helps maintaining the biophysical integrity of tissues and organs. At the same time it plays crucial roles in cellular communication and signalling, with implications in spatial organisation, motility and differentiation. Similarly, the presence of an ECM-like extracellular polymeric substance is known to support and protect bacterial and fungal multicellular aggregates, such as biofilms or colonies. However, the roles and composition of this microbial ECM are still poorly understood. RESULTS: This work presents a protocol to produce S. cerevisiae and C. albicans ECM in an equally highly reproducible manner. Additionally, methodologies for the extraction and fractionation into protein and glycosidic analytical pure fractions were improved. These were subjected to analytical procedures, respectively SDS-PAGE, 2-DE, MALDI-TOF-MS and LC-MS/MS, and DAE and FPLC. Additional chemical methods were also used to test for uronic acids and sulphation. CONCLUSIONS: The methodologies hereby presented were equally efficiently applied to extract high amounts of ECM material from S. cerevisiae and C. albicans mats, therefore showing their robustness and reproducibility for yECM molecular and structural characterization. yECM from S. cerevisiae and C. albicans displayed a different proteome and glycoside fractions. S. cerevisiae yECM presented two well-defined polysaccharides with different mass/charge, and C. albicans ECM presented a single different one. The chemical methods further suggested the presence of uronic acids, and chemical modification, possibly through sulphate substitution. All taken, the procedures herein described present the first sensible and concise approach to the molecular and chemical characterisation of the yeast ECM, opening the way to the in-depth study of the microbe multicellular aggregates structure and life-style.
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spelling pubmed-42190202014-11-05 Methodologies to generate, extract, purify and fractionate yeast ECM for analytical use in proteomics and glycomics Faria-Oliveira, Fábio Carvalho, Joana Belmiro, Celso LR Martinez-Gomariz, Montserrat Hernaez, Maria Luisa Pavão, Mauro Gil, Concha Lucas, Cândida Ferreira, Célia BMC Microbiol Methodology Article BACKGROUND: In a multicellular organism, the extracellular matrix (ECM) provides a cell-supporting scaffold and helps maintaining the biophysical integrity of tissues and organs. At the same time it plays crucial roles in cellular communication and signalling, with implications in spatial organisation, motility and differentiation. Similarly, the presence of an ECM-like extracellular polymeric substance is known to support and protect bacterial and fungal multicellular aggregates, such as biofilms or colonies. However, the roles and composition of this microbial ECM are still poorly understood. RESULTS: This work presents a protocol to produce S. cerevisiae and C. albicans ECM in an equally highly reproducible manner. Additionally, methodologies for the extraction and fractionation into protein and glycosidic analytical pure fractions were improved. These were subjected to analytical procedures, respectively SDS-PAGE, 2-DE, MALDI-TOF-MS and LC-MS/MS, and DAE and FPLC. Additional chemical methods were also used to test for uronic acids and sulphation. CONCLUSIONS: The methodologies hereby presented were equally efficiently applied to extract high amounts of ECM material from S. cerevisiae and C. albicans mats, therefore showing their robustness and reproducibility for yECM molecular and structural characterization. yECM from S. cerevisiae and C. albicans displayed a different proteome and glycoside fractions. S. cerevisiae yECM presented two well-defined polysaccharides with different mass/charge, and C. albicans ECM presented a single different one. The chemical methods further suggested the presence of uronic acids, and chemical modification, possibly through sulphate substitution. All taken, the procedures herein described present the first sensible and concise approach to the molecular and chemical characterisation of the yeast ECM, opening the way to the in-depth study of the microbe multicellular aggregates structure and life-style. BioMed Central 2014-10-25 /pmc/articles/PMC4219020/ /pubmed/25344425 http://dx.doi.org/10.1186/s12866-014-0244-0 Text en © Faria-Oliveira et al.; licensee BioMed Central Ltd. 2014 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Faria-Oliveira, Fábio
Carvalho, Joana
Belmiro, Celso LR
Martinez-Gomariz, Montserrat
Hernaez, Maria Luisa
Pavão, Mauro
Gil, Concha
Lucas, Cândida
Ferreira, Célia
Methodologies to generate, extract, purify and fractionate yeast ECM for analytical use in proteomics and glycomics
title Methodologies to generate, extract, purify and fractionate yeast ECM for analytical use in proteomics and glycomics
title_full Methodologies to generate, extract, purify and fractionate yeast ECM for analytical use in proteomics and glycomics
title_fullStr Methodologies to generate, extract, purify and fractionate yeast ECM for analytical use in proteomics and glycomics
title_full_unstemmed Methodologies to generate, extract, purify and fractionate yeast ECM for analytical use in proteomics and glycomics
title_short Methodologies to generate, extract, purify and fractionate yeast ECM for analytical use in proteomics and glycomics
title_sort methodologies to generate, extract, purify and fractionate yeast ecm for analytical use in proteomics and glycomics
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4219020/
https://www.ncbi.nlm.nih.gov/pubmed/25344425
http://dx.doi.org/10.1186/s12866-014-0244-0
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