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Mass spectrometric protein maps for biomarker discovery and clinical research

Among the wide range of proteomic technologies, targeted mass spectrometry (MS) has shown great potential for biomarker studies. To extend the degree of multiplexing achieved by selected reaction monitoring (SRM), we recently developed SWATH MS. SWATH MS is a variant of the emerging class of data-in...

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Autores principales: Liu, Yansheng, Hüttenhain, Ruth, Collins, Ben, Aebersold, Ruedi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa UK, Ltd. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833812/
https://www.ncbi.nlm.nih.gov/pubmed/24138574
http://dx.doi.org/10.1586/14737159.2013.845089
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author Liu, Yansheng
Hüttenhain, Ruth
Collins, Ben
Aebersold, Ruedi
author_facet Liu, Yansheng
Hüttenhain, Ruth
Collins, Ben
Aebersold, Ruedi
author_sort Liu, Yansheng
collection PubMed
description Among the wide range of proteomic technologies, targeted mass spectrometry (MS) has shown great potential for biomarker studies. To extend the degree of multiplexing achieved by selected reaction monitoring (SRM), we recently developed SWATH MS. SWATH MS is a variant of the emerging class of data-independent acquisition (DIA) methods and essentially converts the molecules in a physical sample into perpetually re-usable digital maps. The thus generated SWATH maps are then mined using a targeted data extraction strategy, allowing us to profile disease-related proteomes at a high degree of reproducibility. The successful application of both SRM and SWATH MS requires the a priori generation of reference spectral maps that provide coordinates for quantification. Herein, we demonstrate that the application of the mass spectrometric reference maps and the acquisition of personalized SWATH maps hold a particular promise for accelerating the current process of biomarker discovery.
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spelling pubmed-38338122013-11-22 Mass spectrometric protein maps for biomarker discovery and clinical research Liu, Yansheng Hüttenhain, Ruth Collins, Ben Aebersold, Ruedi Expert Rev Mol Diagn Review Among the wide range of proteomic technologies, targeted mass spectrometry (MS) has shown great potential for biomarker studies. To extend the degree of multiplexing achieved by selected reaction monitoring (SRM), we recently developed SWATH MS. SWATH MS is a variant of the emerging class of data-independent acquisition (DIA) methods and essentially converts the molecules in a physical sample into perpetually re-usable digital maps. The thus generated SWATH maps are then mined using a targeted data extraction strategy, allowing us to profile disease-related proteomes at a high degree of reproducibility. The successful application of both SRM and SWATH MS requires the a priori generation of reference spectral maps that provide coordinates for quantification. Herein, we demonstrate that the application of the mass spectrometric reference maps and the acquisition of personalized SWATH maps hold a particular promise for accelerating the current process of biomarker discovery. Informa UK, Ltd. 2013-11 2013-10-24 /pmc/articles/PMC3833812/ /pubmed/24138574 http://dx.doi.org/10.1586/14737159.2013.845089 Text en © Informa UK, Ltd.
spellingShingle Review
Liu, Yansheng
Hüttenhain, Ruth
Collins, Ben
Aebersold, Ruedi
Mass spectrometric protein maps for biomarker discovery and clinical research
title Mass spectrometric protein maps for biomarker discovery and clinical research
title_full Mass spectrometric protein maps for biomarker discovery and clinical research
title_fullStr Mass spectrometric protein maps for biomarker discovery and clinical research
title_full_unstemmed Mass spectrometric protein maps for biomarker discovery and clinical research
title_short Mass spectrometric protein maps for biomarker discovery and clinical research
title_sort mass spectrometric protein maps for biomarker discovery and clinical research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833812/
https://www.ncbi.nlm.nih.gov/pubmed/24138574
http://dx.doi.org/10.1586/14737159.2013.845089
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