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Application of mass spectrometry-based proteomics for biomarker discovery in neurological disorders

Mass spectrometry-based quantitative proteomics has emerged as a powerful approach that has the potential to accelerate biomarker discovery, both for diagnostic as well as therapeutic purposes. Proteomics has traditionally been synonymous with 2D gels but is increasingly shifting to the use of gel-f...

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Detalles Bibliográficos
Autores principales: Venugopal, Abhilash, Chaerkady, Raghothama, Pandey, Akhilesh
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811975/
https://www.ncbi.nlm.nih.gov/pubmed/20151002
http://dx.doi.org/10.4103/0972-2327.48845
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author Venugopal, Abhilash
Chaerkady, Raghothama
Pandey, Akhilesh
author_facet Venugopal, Abhilash
Chaerkady, Raghothama
Pandey, Akhilesh
author_sort Venugopal, Abhilash
collection PubMed
description Mass spectrometry-based quantitative proteomics has emerged as a powerful approach that has the potential to accelerate biomarker discovery, both for diagnostic as well as therapeutic purposes. Proteomics has traditionally been synonymous with 2D gels but is increasingly shifting to the use of gel-free systems and liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). Quantitative proteomic approaches have already been applied to investigate various neurological disorders, especially in the context of identifying biomarkers from cerebrospinal fluid and serum. This review highlights the scope of different applications of quantitative proteomics in understanding neurological disorders with special emphasis on biomarker discovery.
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spelling pubmed-28119752010-02-11 Application of mass spectrometry-based proteomics for biomarker discovery in neurological disorders Venugopal, Abhilash Chaerkady, Raghothama Pandey, Akhilesh Ann Indian Acad Neurol Review Article Mass spectrometry-based quantitative proteomics has emerged as a powerful approach that has the potential to accelerate biomarker discovery, both for diagnostic as well as therapeutic purposes. Proteomics has traditionally been synonymous with 2D gels but is increasingly shifting to the use of gel-free systems and liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). Quantitative proteomic approaches have already been applied to investigate various neurological disorders, especially in the context of identifying biomarkers from cerebrospinal fluid and serum. This review highlights the scope of different applications of quantitative proteomics in understanding neurological disorders with special emphasis on biomarker discovery. Medknow Publications 2009 /pmc/articles/PMC2811975/ /pubmed/20151002 http://dx.doi.org/10.4103/0972-2327.48845 Text en © Annals of Indian Academy of Neurology http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Venugopal, Abhilash
Chaerkady, Raghothama
Pandey, Akhilesh
Application of mass spectrometry-based proteomics for biomarker discovery in neurological disorders
title Application of mass spectrometry-based proteomics for biomarker discovery in neurological disorders
title_full Application of mass spectrometry-based proteomics for biomarker discovery in neurological disorders
title_fullStr Application of mass spectrometry-based proteomics for biomarker discovery in neurological disorders
title_full_unstemmed Application of mass spectrometry-based proteomics for biomarker discovery in neurological disorders
title_short Application of mass spectrometry-based proteomics for biomarker discovery in neurological disorders
title_sort application of mass spectrometry-based proteomics for biomarker discovery in neurological disorders
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811975/
https://www.ncbi.nlm.nih.gov/pubmed/20151002
http://dx.doi.org/10.4103/0972-2327.48845
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