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Recent development of multi-dimensional chromatography strategies in proteome research()

As a complementary approach to two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), multi-dimensional chromatography separation methods have been widely applied in all kinds of biological sample investigations. Multi-dimensional liquid chromatography (MDLC) coupled with bio-mass spectrometr...

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Autores principales: Tang, Jia, Gao, Mingxia, Deng, Chunhui, Zhang, Xiangming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185551/
https://www.ncbi.nlm.nih.gov/pubmed/18289947
http://dx.doi.org/10.1016/j.jchromb.2008.01.029
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author Tang, Jia
Gao, Mingxia
Deng, Chunhui
Zhang, Xiangming
author_facet Tang, Jia
Gao, Mingxia
Deng, Chunhui
Zhang, Xiangming
author_sort Tang, Jia
collection PubMed
description As a complementary approach to two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), multi-dimensional chromatography separation methods have been widely applied in all kinds of biological sample investigations. Multi-dimensional liquid chromatography (MDLC) coupled with bio-mass spectrometry (MS) is playing important roles in proteome research due to its high speed, high resolution and high sensitivity. Proteome analysis strategies mainly include bottom-up and top-down approaches which carry out biological sample separation based on peptide and protein levels, respectively. Electrophoretic methods combined with liquid chromatography like IEF-HPLC and HPLC-SDS-PAGE have been successful applied for protein separations. As for MDLC strategy, ion-exchange chromatography (IEX) together with reversed phase liquid chromatography (RPLC) is still a most widely used chromatography in proteome analysis, other chromatographic methods are also frequently used in protein pre-fractionations, while affinity chromatography is usually adopted for specific functional protein analysis. Recent MDLC technologies and applications to variety of proteome analysis have been achieved great development. A digest peptide-based approach as so-called “bottom-up” and intact protein-based approach “top-down” analysis of proteome samples were briefly reviewed in this paper. The diversity of combinations of different chromatography modes to set up MDLC systems was demonstrated and discussed. Novel developments of MDLC techniques such as high-abundance protein depletion and chromatography array were also included in this review.
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spelling pubmed-71855512020-04-28 Recent development of multi-dimensional chromatography strategies in proteome research() Tang, Jia Gao, Mingxia Deng, Chunhui Zhang, Xiangming J Chromatogr B Analyt Technol Biomed Life Sci Article As a complementary approach to two-dimensional polyacrylamide gel electrophoresis (2D-PAGE), multi-dimensional chromatography separation methods have been widely applied in all kinds of biological sample investigations. Multi-dimensional liquid chromatography (MDLC) coupled with bio-mass spectrometry (MS) is playing important roles in proteome research due to its high speed, high resolution and high sensitivity. Proteome analysis strategies mainly include bottom-up and top-down approaches which carry out biological sample separation based on peptide and protein levels, respectively. Electrophoretic methods combined with liquid chromatography like IEF-HPLC and HPLC-SDS-PAGE have been successful applied for protein separations. As for MDLC strategy, ion-exchange chromatography (IEX) together with reversed phase liquid chromatography (RPLC) is still a most widely used chromatography in proteome analysis, other chromatographic methods are also frequently used in protein pre-fractionations, while affinity chromatography is usually adopted for specific functional protein analysis. Recent MDLC technologies and applications to variety of proteome analysis have been achieved great development. A digest peptide-based approach as so-called “bottom-up” and intact protein-based approach “top-down” analysis of proteome samples were briefly reviewed in this paper. The diversity of combinations of different chromatography modes to set up MDLC systems was demonstrated and discussed. Novel developments of MDLC techniques such as high-abundance protein depletion and chromatography array were also included in this review. Elsevier B.V. 2008-04-15 2008-02-02 /pmc/articles/PMC7185551/ /pubmed/18289947 http://dx.doi.org/10.1016/j.jchromb.2008.01.029 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 Article
Tang, Jia
Gao, Mingxia
Deng, Chunhui
Zhang, Xiangming
Recent development of multi-dimensional chromatography strategies in proteome research()
title Recent development of multi-dimensional chromatography strategies in proteome research()
title_full Recent development of multi-dimensional chromatography strategies in proteome research()
title_fullStr Recent development of multi-dimensional chromatography strategies in proteome research()
title_full_unstemmed Recent development of multi-dimensional chromatography strategies in proteome research()
title_short Recent development of multi-dimensional chromatography strategies in proteome research()
title_sort recent development of multi-dimensional chromatography strategies in proteome research()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185551/
https://www.ncbi.nlm.nih.gov/pubmed/18289947
http://dx.doi.org/10.1016/j.jchromb.2008.01.029
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