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High-resolution separations of protein isoforms with liquid chromatography time-of-flight mass spectrometry using polymer monolithic capillary columns
被引:49
作者:
Eeltink, Sebastiaan
[1
]
Wouters, Bert
[1
]
Desmet, Gert
[1
]
Ursem, Mario
[2
]
Blinco, David
[3
]
Kemp, Glenwyn D.
[3
]
Treumann, Achim
[3
]
机构:
[1] Vrije Univ Brussel, Dept Chem Engn, B-1050 Brussels, Belgium
[2] Dionex Chem Corp, NL-1046 AA Amsterdam, Netherlands
[3] NEPAF, Newcastle Upon Tyne, Tyne & Wear, England
关键词:
Top-down proteomics;
Protein isoforms;
Monolithic columns;
ABRF proteomics standard;
COLLISION-INDUCED DISSOCIATION;
ELECTRON-TRANSFER DISSOCIATION;
REVERSED-PHASE CHROMATOGRAPHY;
TOP-DOWN PROTEOMICS;
INTACT PROTEINS;
MACROPOROUS POLY(STYRENE-CO-DIVINYLBENZENE);
MS;
IDENTIFICATION;
PEPTIDES;
DIGESTS;
D O I:
10.1016/j.chroma.2011.06.049
中图分类号:
Q5 [生物化学];
学科分类号:
070307 [化学生物学];
摘要:
The separation of intact proteins, including protein isoforms arising from various amino-acid modifications, employing a poly(styrene-co-divinylbenzene) monolithic capillary column in high-performance liquid chromatography coupled on-line to a time-of-flight mass spectrometer (MS) is described. Using a 250 mm x 0.2 mm monolithic capillary column high-sensitivity separations yielding peak capacities of >600 were achieved with a 2 h linear gradient and formic acid added in the mobile phase as ion-pairing agent. The combination of high-resolution chromatography with high-accuracy MS allowed to distinguish protein isoforms that differ only in their oxidation and biotinylation state allowing the separation between structural isoforms. Finally, the potential to separate proteins isoforms due to glycosylation is discussed. (C) 2011 Elsevier B.V. All rights reserved.
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页码:5504 / 5511
页数:8
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