Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Culurgioni, Simone, Tang, Minzhe, Hall, David R., Walsh, Martin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2017
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
_version_ 1783290100676820992
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
work_keys_str_mv AT culurgionisimone biochemicalandstructuralcharacterizationofthecarbohydratetransportsubstratebindingproteinsp0092
AT tangminzhe biochemicalandstructuralcharacterizationofthecarbohydratetransportsubstratebindingproteinsp0092
AT halldavidr biochemicalandstructuralcharacterizationofthecarbohydratetransportsubstratebindingproteinsp0092
AT walshmartina biochemicalandstructuralcharacterizationofthecarbohydratetransportsubstratebindingproteinsp0092