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Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092
Development of new antimicrobials and vaccines for Streptococcus pneumoniae (pneumococcus) are necessary to halt the rapid rise in multiple resistant strains. Carbohydrate substrate binding proteins (SBPs) represent viable targets for the development of protein-based vaccines and new antimicrobials...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752355/ https://www.ncbi.nlm.nih.gov/pubmed/28994793 http://dx.doi.org/10.3791/56294 |
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author | Culurgioni, Simone Tang, Minzhe Hall, David R. Walsh, Martin A. |
author_facet | Culurgioni, Simone Tang, Minzhe Hall, David R. Walsh, Martin A. |
author_sort | Culurgioni, Simone |
collection | PubMed |
description | Development of new antimicrobials and vaccines for Streptococcus pneumoniae (pneumococcus) are necessary to halt the rapid rise in multiple resistant strains. Carbohydrate substrate binding proteins (SBPs) represent viable targets for the development of protein-based vaccines and new antimicrobials because of their extracellular localization and the centrality of carbohydrate import for pneumococcal metabolism, respectively. Described here is a rationalized integrated protocol to carry out a comprehensive characterization of SP0092, which can be extended to other carbohydrate SBPs from the pneumococcus and other bacteria. This procedure can aid the structure-based design of inhibitors for this class of proteins. Presented in the first part of this manuscript are protocols for biochemical analysis by thermal shift assay, multi angle light scattering (MALS), and size exclusion chromatography (SEC), which optimize the stability and homogeneity of the sample directed to crystallization trials and so enhance the probability of success. The second part of this procedure describes the characterization of the SBP crystals using a tunable wavelength anomalous diffraction synchrotron beamline, and data collection protocols for measuring data that can be used to resolve the crystallized protein structure. |
format | Online Article Text |
id | pubmed-5752355 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-57523552018-01-19 Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092 Culurgioni, Simone Tang, Minzhe Hall, David R. Walsh, Martin A. J Vis Exp Biochemistry Development of new antimicrobials and vaccines for Streptococcus pneumoniae (pneumococcus) are necessary to halt the rapid rise in multiple resistant strains. Carbohydrate substrate binding proteins (SBPs) represent viable targets for the development of protein-based vaccines and new antimicrobials because of their extracellular localization and the centrality of carbohydrate import for pneumococcal metabolism, respectively. Described here is a rationalized integrated protocol to carry out a comprehensive characterization of SP0092, which can be extended to other carbohydrate SBPs from the pneumococcus and other bacteria. This procedure can aid the structure-based design of inhibitors for this class of proteins. Presented in the first part of this manuscript are protocols for biochemical analysis by thermal shift assay, multi angle light scattering (MALS), and size exclusion chromatography (SEC), which optimize the stability and homogeneity of the sample directed to crystallization trials and so enhance the probability of success. The second part of this procedure describes the characterization of the SBP crystals using a tunable wavelength anomalous diffraction synchrotron beamline, and data collection protocols for measuring data that can be used to resolve the crystallized protein structure. MyJove Corporation 2017-10-02 /pmc/articles/PMC5752355/ /pubmed/28994793 http://dx.doi.org/10.3791/56294 Text en Copyright © 2017, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Biochemistry Culurgioni, Simone Tang, Minzhe Hall, David R. Walsh, Martin A. Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092 |
title | Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092 |
title_full | Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092 |
title_fullStr | Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092 |
title_full_unstemmed | Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092 |
title_short | Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092 |
title_sort | biochemical and structural characterization of the carbohydrate transport substrate-binding-protein sp0092 |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5752355/ https://www.ncbi.nlm.nih.gov/pubmed/28994793 http://dx.doi.org/10.3791/56294 |
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