
DOI . ORG {
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Title[redir]:
Taking the Shortcut for High-Throughput Shotgun Proteomic Analysis of Bacteria | SpringerLink
Description:
Currently, proteomic tools are able to establish a complete list of the most abundant proteins present in a sample, providing the opportunity to study at high resolution the physiology of any bacteria for which the genome sequence is available. For a comprehensive...
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Keywords {đ}
pubmed, proteomics, article, google, scholar, cas, armengaud, protocol, shotgun, proteomic, bacteria, central, analysis, information, proteome, privacy, cookies, content, publish, chapter, data, research, search, highthroughput, allain, methods, mass, protein, christieoleza, mol, cell, download, france, springer, usd, processing, personal, log, journal, hostbacteria, interactions, shortcut, hartmann, françois, gaillard, pible, jean, book, biology, list,
Topics {âď¸}
shotgun nanolc-ms/ms proteogenomics month download article/chapter mass spectrometry-based analysis document maldi-tof biomarkers host-bacteria interactions relative protein abundance privacy choices/manage cookies high-throughput proteomics host-pathogen interaction device instant download quantitative proteomic analysis ms/ms spectra kowalak ja differential shotgun proteomics spectral count approach author information authors editor information editors jean-charles gaillard european economic area pina-villalonga jm restricting fermentative potential virulence factors produced early secretome profiling multiple significance testing aux energies alternatives anne-hÊlène davin bagnols-sur-cèze montigny-le-bretonneux journal finder publish conditions privacy policy comparative proteomic approach resulting peptide mixtures adaptive strategy evidenced protocol hartmann investigating pathogen biology yates jr 3rd accepting optional cookies strain-level typing abundant proteins present main content log subsequent data processing protocol usd 49 bacteria protocol o'callaghan bmc bioinformatics 9 host perspective shotgun proteomics protocol cite social media permissions reprints
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- Kraut A, Marcellin M, Adrait A, Kuhn L, Louwagie M, Kieffer-Jaquinod S et al (2009) Peptide storage: are you getting the best return on your investment?
Schema {đşď¸}
ScholarlyArticle:
headline:Taking the Shortcut for High-Throughput Shotgun Proteomic Analysis of Bacteria
pageEnd:285
pageStart:275
image:https://media.springernature.com/w153/springer-static/cover/book/978-1-4939-1261-2.jpg
genre:
Springer Protocols
isPartOf:
name:Host-Bacteria Interactions
isbn:
978-1-4939-1261-2
978-1-4939-1260-5
type:Book
publisher:
name:Springer New York
logo:
url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
type:ImageObject
type:Organization
author:
name:Erica Marie Hartmann
affiliation:
name:CEA, DSV, IBEB
address:
name:Lab Biochim System Perturb, CEA, DSV, IBEB, Bagnols-sur-Cèze, France
type:PostalAddress
type:Organization
type:Person
name:François Allain
affiliation:
name:CEA, DSV, IBEB
address:
name:Lab Biochim System Perturb, CEA, DSV, IBEB, Bagnols-sur-Cèze, France
type:PostalAddress
type:Organization
name:Bertin Technologies, Parc dâactivitĂŠs du Pas du Lac
address:
name:Bertin Technologies, Parc dâactivitĂŠs du Pas du Lac, Montigny-le-Bretonneux, France
type:PostalAddress
type:Organization
type:Person
name:Jean-Charles Gaillard
affiliation:
name:CEA, DSV, IBEB
address:
name:Lab Biochim System Perturb, CEA, DSV, IBEB, Bagnols-sur-Cèze, France
type:PostalAddress
type:Organization
type:Person
name:Olivier Pible
affiliation:
name:CEA, DSV, IBEB
address:
name:Lab Biochim System Perturb, CEA, DSV, IBEB, Bagnols-sur-Cèze, France
type:PostalAddress
type:Organization
type:Person
name:Jean Armengaud
affiliation:
name:CEA, DSV, IBEB
address:
name:Lab Biochim System Perturb, CEA, DSV, IBEB, Bagnols-sur-Cèze, France
type:PostalAddress
type:Organization
email:[email protected]
type:Person
keywords:High-throughput proteomics, Quantitative proteomics, Bacterial proteome, Spectral count, Tandem mass spectrometry
description:Currently, proteomic tools are able to establish a complete list of the most abundant proteins present in a sample, providing the opportunity to study at high resolution the physiology of any bacteria for which the genome sequence is available. For a comprehensive list, proteins should be first resolved into fractions that are then proteolyzed by trypsin. The resulting peptide mixtures are analyzed by a high-throughput tandem mass spectrometer that records thousands of MS/MS spectra for each fraction. These spectra are then assigned to peptides, which are used as evidence of the existence of proteins. In addition to generating a list of protein identifications, this shortcut to proteomics uses the number of spectra recorded for each protein to quantify the observations. Here, we describe one of the most simple sample preparation methods for high-throughput proteomics of bacteria, as well as the subsequent data processing to extract quantitative information based on the spectral count approach.
datePublished:2014
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Person:
name:Erica Marie Hartmann
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name:CEA, DSV, IBEB
address:
name:Lab Biochim System Perturb, CEA, DSV, IBEB, Bagnols-sur-Cèze, France
type:PostalAddress
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name:François Allain
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type:PostalAddress
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