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Hydrophilic interaction liquid chromatography (HILIC) in proteomics

In proteomics, nanoflow multidimensional chromatography is now the gold standard for the separation of complex mixtures of peptides as generated by in-solution digestion of whole-cell lysates. Ideally, the different stationary phases used in multidimensional chromatography should provide orthogonal...

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Detalles Bibliográficos
Autores principales: Boersema, Paul J., Mohammed, Shabaz, Heck, Albert J. R.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2324128/
https://www.ncbi.nlm.nih.gov/pubmed/18264818
http://dx.doi.org/10.1007/s00216-008-1865-7
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author Boersema, Paul J.
Mohammed, Shabaz
Heck, Albert J. R.
author_facet Boersema, Paul J.
Mohammed, Shabaz
Heck, Albert J. R.
author_sort Boersema, Paul J.
collection PubMed
description In proteomics, nanoflow multidimensional chromatography is now the gold standard for the separation of complex mixtures of peptides as generated by in-solution digestion of whole-cell lysates. Ideally, the different stationary phases used in multidimensional chromatography should provide orthogonal separation characteristics. For this reason, the combination of strong cation exchange chromatography (SCX) and reversed-phase (RP) chromatography is the most widely used combination for the separation of peptides. Here, we review the potential of hydrophilic interaction liquid chromatography (HILIC) as a separation tool in the multidimensional separation of peptides in proteomics applications. Recent work has revealed that HILIC may provide an excellent alternative to SCX, possessing several advantages in the area of separation power and targeted analysis of protein post-translational modifications. [Figure: see text]
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spelling pubmed-23241282008-04-22 Hydrophilic interaction liquid chromatography (HILIC) in proteomics Boersema, Paul J. Mohammed, Shabaz Heck, Albert J. R. Anal Bioanal Chem Review In proteomics, nanoflow multidimensional chromatography is now the gold standard for the separation of complex mixtures of peptides as generated by in-solution digestion of whole-cell lysates. Ideally, the different stationary phases used in multidimensional chromatography should provide orthogonal separation characteristics. For this reason, the combination of strong cation exchange chromatography (SCX) and reversed-phase (RP) chromatography is the most widely used combination for the separation of peptides. Here, we review the potential of hydrophilic interaction liquid chromatography (HILIC) as a separation tool in the multidimensional separation of peptides in proteomics applications. Recent work has revealed that HILIC may provide an excellent alternative to SCX, possessing several advantages in the area of separation power and targeted analysis of protein post-translational modifications. [Figure: see text] Springer-Verlag 2008-02-09 2008-05 /pmc/articles/PMC2324128/ /pubmed/18264818 http://dx.doi.org/10.1007/s00216-008-1865-7 Text en © The Author(s) 2008
spellingShingle Review
Boersema, Paul J.
Mohammed, Shabaz
Heck, Albert J. R.
Hydrophilic interaction liquid chromatography (HILIC) in proteomics
title Hydrophilic interaction liquid chromatography (HILIC) in proteomics
title_full Hydrophilic interaction liquid chromatography (HILIC) in proteomics
title_fullStr Hydrophilic interaction liquid chromatography (HILIC) in proteomics
title_full_unstemmed Hydrophilic interaction liquid chromatography (HILIC) in proteomics
title_short Hydrophilic interaction liquid chromatography (HILIC) in proteomics
title_sort hydrophilic interaction liquid chromatography (hilic) in proteomics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2324128/
https://www.ncbi.nlm.nih.gov/pubmed/18264818
http://dx.doi.org/10.1007/s00216-008-1865-7
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