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Study of structure-dependent chromatographic behavior of glycopeptides using reversed phase nanoLC
P. Kozlik, R. Goldman, M. Sanda,
Language English Country Germany
Document type Journal Article
- MeSH
- Chromatography, Reverse-Phase methods MeSH
- Glycopeptides blood chemistry metabolism MeSH
- Glycosylation MeSH
- Humans MeSH
- Nanotechnology methods MeSH
- Peptide Fragments analysis chemistry metabolism MeSH
- Proteomics MeSH
- Sensitivity and Specificity MeSH
- Trypsin metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Analysis of glycosylation is challenging due to micro- and macro-heterogeneity of the protein attachment. A combination of LC with MS/MS is one of the most powerful tools for glycopeptide analysis. In this work, we show the effect of various monosaccharide units on the retention time of glycopeptides. Retention behavior of several glycoforms of six peptides obtained from tryptic digest of haptoglobin, hemopexin, and sex hormone-binding globulin was studied on a reversed phase chromatographic column. We observed reduction of the retention time with increasing number of monosaccharide units of glycans attached to the same peptide backbone. Fucosylation of larger glycans provides less significant retention time shift than for smaller ones. Retention times of glycopeptides were expressed as relative retention times. These relative retention times were used for calculation of upper and lower limits of glycopeptide retention time windows under the reversed phase conditions. We then demonstrated on the case of a glycopeptide of haptoglobin that the predicted retention time window boosts confidence of identification and minimizes false-positive identification. Relative retention time, as a qualitative parameter, is expected to improve LC-MS/MS characterization of glycopeptides.
References provided by Crossref.org
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- $a Kozlik, Petr $u Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA. Department of Analytical Chemistry, Faculty of Science, Charles University, Czech Republic.
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- $a Analysis of glycosylation is challenging due to micro- and macro-heterogeneity of the protein attachment. A combination of LC with MS/MS is one of the most powerful tools for glycopeptide analysis. In this work, we show the effect of various monosaccharide units on the retention time of glycopeptides. Retention behavior of several glycoforms of six peptides obtained from tryptic digest of haptoglobin, hemopexin, and sex hormone-binding globulin was studied on a reversed phase chromatographic column. We observed reduction of the retention time with increasing number of monosaccharide units of glycans attached to the same peptide backbone. Fucosylation of larger glycans provides less significant retention time shift than for smaller ones. Retention times of glycopeptides were expressed as relative retention times. These relative retention times were used for calculation of upper and lower limits of glycopeptide retention time windows under the reversed phase conditions. We then demonstrated on the case of a glycopeptide of haptoglobin that the predicted retention time window boosts confidence of identification and minimizes false-positive identification. Relative retention time, as a qualitative parameter, is expected to improve LC-MS/MS characterization of glycopeptides.
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