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Online coupling of reverse-phase and hydrophilic interaction liquid chromatography for protein and glycoprotein characterization

We have developed a novel system for coupling reverse-phase (RP) and hydrophilic interaction liquid chromatography (HILIC) online in a micro-flow scheme. In this approach, the inherent solvent incompatibility between RP and HILIC is overcome through the use of constant-pressure online solvent mixing...

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Detalles Bibliográficos
Autores principales: Lam, Maggie P. Y., Siu, S. O., Lau, Edward, Mao, Xiuli, Sun, H. Z., Chiu, Philip C. N., Yeung, William S. B., Cox, David M., Chu, Ivan K.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2939347/
https://www.ncbi.nlm.nih.gov/pubmed/20632160
http://dx.doi.org/10.1007/s00216-010-3991-2
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author Lam, Maggie P. Y.
Siu, S. O.
Lau, Edward
Mao, Xiuli
Sun, H. Z.
Chiu, Philip C. N.
Yeung, William S. B.
Cox, David M.
Chu, Ivan K.
author_facet Lam, Maggie P. Y.
Siu, S. O.
Lau, Edward
Mao, Xiuli
Sun, H. Z.
Chiu, Philip C. N.
Yeung, William S. B.
Cox, David M.
Chu, Ivan K.
author_sort Lam, Maggie P. Y.
collection PubMed
description We have developed a novel system for coupling reverse-phase (RP) and hydrophilic interaction liquid chromatography (HILIC) online in a micro-flow scheme. In this approach, the inherent solvent incompatibility between RP and HILIC is overcome through the use of constant-pressure online solvent mixing, which allows our system to perform efficient separations of both hydrophilic and hydrophobic compounds for mass spectrometry-based proteomics applications. When analyzing the tryptic digests of bovine serum albumin, ribonuclease B, and horseradish peroxidase, we observed near-identical coverage of peptides and glycopeptides when using online RP-HILIC—with only a single sample injection event—as we did from two separate RP and HILIC analyses. The coupled system was also capable of concurrently characterizing the peptide and glycan portions of deglycosylated glycoproteins from one injection event, as confirmed, for example, through our detection of 23 novel glycans from turkey ovalbumin. Finally, we validated the applicability of using RP-HILIC for the analysis of highly complex biological samples (mouse chondrocyte lysate, deglycosylated human serum). The enhanced coverage and efficiency of online RP-HILIC makes it a viable technique for the comprehensive separation of components displaying dramatically different hydrophobicities, such as peptides, glycopeptides, and glycans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-010-3991-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-29393472010-10-05 Online coupling of reverse-phase and hydrophilic interaction liquid chromatography for protein and glycoprotein characterization Lam, Maggie P. Y. Siu, S. O. Lau, Edward Mao, Xiuli Sun, H. Z. Chiu, Philip C. N. Yeung, William S. B. Cox, David M. Chu, Ivan K. Anal Bioanal Chem Original Paper We have developed a novel system for coupling reverse-phase (RP) and hydrophilic interaction liquid chromatography (HILIC) online in a micro-flow scheme. In this approach, the inherent solvent incompatibility between RP and HILIC is overcome through the use of constant-pressure online solvent mixing, which allows our system to perform efficient separations of both hydrophilic and hydrophobic compounds for mass spectrometry-based proteomics applications. When analyzing the tryptic digests of bovine serum albumin, ribonuclease B, and horseradish peroxidase, we observed near-identical coverage of peptides and glycopeptides when using online RP-HILIC—with only a single sample injection event—as we did from two separate RP and HILIC analyses. The coupled system was also capable of concurrently characterizing the peptide and glycan portions of deglycosylated glycoproteins from one injection event, as confirmed, for example, through our detection of 23 novel glycans from turkey ovalbumin. Finally, we validated the applicability of using RP-HILIC for the analysis of highly complex biological samples (mouse chondrocyte lysate, deglycosylated human serum). The enhanced coverage and efficiency of online RP-HILIC makes it a viable technique for the comprehensive separation of components displaying dramatically different hydrophobicities, such as peptides, glycopeptides, and glycans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-010-3991-2) contains supplementary material, which is available to authorized users. Springer-Verlag 2010-07-15 2010 /pmc/articles/PMC2939347/ /pubmed/20632160 http://dx.doi.org/10.1007/s00216-010-3991-2 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Lam, Maggie P. Y.
Siu, S. O.
Lau, Edward
Mao, Xiuli
Sun, H. Z.
Chiu, Philip C. N.
Yeung, William S. B.
Cox, David M.
Chu, Ivan K.
Online coupling of reverse-phase and hydrophilic interaction liquid chromatography for protein and glycoprotein characterization
title Online coupling of reverse-phase and hydrophilic interaction liquid chromatography for protein and glycoprotein characterization
title_full Online coupling of reverse-phase and hydrophilic interaction liquid chromatography for protein and glycoprotein characterization
title_fullStr Online coupling of reverse-phase and hydrophilic interaction liquid chromatography for protein and glycoprotein characterization
title_full_unstemmed Online coupling of reverse-phase and hydrophilic interaction liquid chromatography for protein and glycoprotein characterization
title_short Online coupling of reverse-phase and hydrophilic interaction liquid chromatography for protein and glycoprotein characterization
title_sort online coupling of reverse-phase and hydrophilic interaction liquid chromatography for protein and glycoprotein characterization
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2939347/
https://www.ncbi.nlm.nih.gov/pubmed/20632160
http://dx.doi.org/10.1007/s00216-010-3991-2
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