Analysis of N-glycans from recombinant immunoglobulin G by on-line reversed-phase high-performance liquid chromatography/mass spectrometry
An on-line reversed-phase (RP) high-performance liquid chromatography/mass spectrometry (MS) method has been developed for profiling and characterizing N-glycans from recombinant immunoglobulin G antibodies. In this method, released N-glycans are derivatized at their reducing end with 2-aminobenzami...
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Veröffentlicht in: | Analytical biochemistry 2007-11, Vol.370 (2), p.147-161 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | An on-line reversed-phase (RP) high-performance liquid chromatography/mass spectrometry (MS) method has been developed for profiling and characterizing
N-glycans from recombinant immunoglobulin G antibodies. In this method, released
N-glycans are derivatized at their reducing end with 2-aminobenzamide (2AB) and separated on a RP column with on-line fluorescence and MS detection. The method achieves good resolution of all major glycans and segregates glycan types (high-mannose, hybrid, and complex) to different regions of the chromatogram, thus allowing accurate quantification of
N-glycans from the fluorescent signal alone. Moreover, the mobile phase used allows high quality on-line MS detection. The 2AB-labeled
N-glycans demonstrate good ionization efficiency in electrospray and generate primarily doubly charged [M+2H]
2+ ions. The mass and structural information can be readily obtained from the on-line MS and tandem MS data. As little as 70 fmol glycan species can be detected and identified. |
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ISSN: | 0003-2697 1096-0309 |
DOI: | 10.1016/j.ab.2007.08.012 |