2013
DOI: 10.1177/2211068212454738
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Automated Mass Spectrometry–Based Functional Assay for the Routine Analysis of the Secretome

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Cited by 52 publications
(39 citation statements)
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“…The gels were then stained with Coomassie blue, and the most intense bands were excised and digested with trypsin. Digested proteins were then analyzed by nanoliquid chromatography tandem mass spectrometry (nano LC-MS/MS) using a Nano Acquity UPLC coupled to a QTOF Micro mass spectrometer, according to published procedures [13][14][15][16][17][18][19]. The raw data were processed using Protein Lynx Global Server (PLGS, version 2.4) and the resulting pkl files were submitted to Mascot database search [13][14][15][16][17][18][19].…”
Section: Methodsmentioning
confidence: 99%
“…The gels were then stained with Coomassie blue, and the most intense bands were excised and digested with trypsin. Digested proteins were then analyzed by nanoliquid chromatography tandem mass spectrometry (nano LC-MS/MS) using a Nano Acquity UPLC coupled to a QTOF Micro mass spectrometer, according to published procedures [13][14][15][16][17][18][19]. The raw data were processed using Protein Lynx Global Server (PLGS, version 2.4) and the resulting pkl files were submitted to Mascot database search [13][14][15][16][17][18][19].…”
Section: Methodsmentioning
confidence: 99%
“…Due to high-performing MS instruments, simplified analytical workflows and versatile data analysis, mass spectrometry is applicable to almost every area of the life sciences and potentially even far beyond [5154]. The two most common ionization methods are electrospray ionization (ESI) and matrix-assisted laser desorption/ionization (MALDI).…”
Section: Reviewmentioning
confidence: 99%
“…For visualization of protein bands, the gel can be stained either with the dye coomassie blue or silver stained or by fluorescently labeling the samples before 2-DE. For mass spectrometry analysis, gel bands are removed, and undergo several other steps to generate peptides in bottom-up and shotgun proteomics [51, 53, 67, 68]. Compared to LC/MS, 2-DE methods are more reproducible and robust.…”
Section: Reviewmentioning
confidence: 99%
“…MS is a method that can reliably and comprehensively identify proteins and putative biomarkers [4,5,[12][13][14][15][16][17][18][19][20][21][22]. MS is already in use for newborn screening for several other disorders, including phenylketonuria, congenital hypothyroidism and cystic fibrosis [23].…”
Section: Introductionmentioning
confidence: 99%