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Quantitative mass spectrometry-based techniques for clinical use: Biomarker identification and quantification()
The potential for development of personalised medicine through the characterisation of novel biomarkers is an exciting prospect for improved patient care. Recent advances in mass spectrometric (MS) techniques, liquid phase analyte separation and bioinformatic tools for high throughput now mean that...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185464/ https://www.ncbi.nlm.nih.gov/pubmed/19058768 http://dx.doi.org/10.1016/j.jchromb.2008.11.023 |
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author | Simpson, Kathryn L. Whetton, Anthony D. Dive, Caroline |
author_facet | Simpson, Kathryn L. Whetton, Anthony D. Dive, Caroline |
author_sort | Simpson, Kathryn L. |
collection | PubMed |
description | The potential for development of personalised medicine through the characterisation of novel biomarkers is an exciting prospect for improved patient care. Recent advances in mass spectrometric (MS) techniques, liquid phase analyte separation and bioinformatic tools for high throughput now mean that this goal may soon become a reality. However, there are challenges to be overcome for the identification and validation of robust biomarkers. Bio-fluids such as plasma and serum are a rich source of protein, many of which may reflect disease status, and due to the ease of sampling and handling, novel blood borne biomarkers are very much sought after. MS-based methods for high throughput protein identification and quantification are now available such that the issues arising from the huge dynamic range of proteins present in plasma may be overcome, allowing deep mining of the blood proteome to reveal novel biomarker signatures for clinical use. In addition, the development of sensitive MS-based methods for biomarker validation may bypass the bottleneck created by the need for generation and usage of reliable antibodies prior to large scale screening. In this review, we discuss the MS-based methods that are available for clinical proteomic analysis and highlight the progress made and future challenges faced in this cutting edge area of research. |
format | Online Article Text |
id | pubmed-7185464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71854642020-04-28 Quantitative mass spectrometry-based techniques for clinical use: Biomarker identification and quantification() Simpson, Kathryn L. Whetton, Anthony D. Dive, Caroline J Chromatogr B Analyt Technol Biomed Life Sci Review The potential for development of personalised medicine through the characterisation of novel biomarkers is an exciting prospect for improved patient care. Recent advances in mass spectrometric (MS) techniques, liquid phase analyte separation and bioinformatic tools for high throughput now mean that this goal may soon become a reality. However, there are challenges to be overcome for the identification and validation of robust biomarkers. Bio-fluids such as plasma and serum are a rich source of protein, many of which may reflect disease status, and due to the ease of sampling and handling, novel blood borne biomarkers are very much sought after. MS-based methods for high throughput protein identification and quantification are now available such that the issues arising from the huge dynamic range of proteins present in plasma may be overcome, allowing deep mining of the blood proteome to reveal novel biomarker signatures for clinical use. In addition, the development of sensitive MS-based methods for biomarker validation may bypass the bottleneck created by the need for generation and usage of reliable antibodies prior to large scale screening. In this review, we discuss the MS-based methods that are available for clinical proteomic analysis and highlight the progress made and future challenges faced in this cutting edge area of research. Elsevier B.V. 2009-05-01 2008-11-18 /pmc/articles/PMC7185464/ /pubmed/19058768 http://dx.doi.org/10.1016/j.jchromb.2008.11.023 Text en Copyright © 2008 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Review Simpson, Kathryn L. Whetton, Anthony D. Dive, Caroline Quantitative mass spectrometry-based techniques for clinical use: Biomarker identification and quantification() |
title | Quantitative mass spectrometry-based techniques for clinical use: Biomarker identification and quantification() |
title_full | Quantitative mass spectrometry-based techniques for clinical use: Biomarker identification and quantification() |
title_fullStr | Quantitative mass spectrometry-based techniques for clinical use: Biomarker identification and quantification() |
title_full_unstemmed | Quantitative mass spectrometry-based techniques for clinical use: Biomarker identification and quantification() |
title_short | Quantitative mass spectrometry-based techniques for clinical use: Biomarker identification and quantification() |
title_sort | quantitative mass spectrometry-based techniques for clinical use: biomarker identification and quantification() |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185464/ https://www.ncbi.nlm.nih.gov/pubmed/19058768 http://dx.doi.org/10.1016/j.jchromb.2008.11.023 |
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