Glycan-specific precipitation of glycopeptides in high organic content sample solvents used in HILIC
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
R01 CA135069
NCI NIH HHS - United States
R01 CA238455
NCI NIH HHS - United States
S10 OD023557
NIH HHS - United States
U01 CA230692
NCI NIH HHS - United States
PubMed
32485649
PubMed Central
PMC7305521
DOI
10.1016/j.jchromb.2020.122196
PII: S1570-0232(20)30275-0
Knihovny.cz E-zdroje
- Klíčová slova
- Glycopeptides, Hydrophilic interaction liquid chromatography, Solubility,
- MeSH
- acetonitrily chemie MeSH
- glykopeptidy analýza chemie izolace a purifikace MeSH
- hydrofobní a hydrofilní interakce MeSH
- kyselina N-acetylneuraminová chemie MeSH
- polysacharidy chemie MeSH
- rozpouštědla chemie MeSH
- vysokoúčinná kapalinová chromatografie metody MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- acetonitrile MeSH Prohlížeč
- acetonitrily MeSH
- glykopeptidy MeSH
- kyselina N-acetylneuraminová MeSH
- polysacharidy MeSH
- rozpouštědla MeSH
The composition of a sample solvent has a crucial impact on separations in hydrophilic interaction liquid chromatography (HILIC). In this short communication, we studied the effect of an organic modifier in the sample solvent on the solubility of different tryptic glycopeptides of hemopexin and haptoglobin proteins. The results showed that the solubility of glycopeptides in solvents with a high acetonitrile content depends on the type of attached N-glycan. We observed lower solubility in larger glycans attached to the same peptide backbone, and we demonstrated that glycopeptides containing sialic acids precipitate more readily than those without sialic acid. Therefore, the sample solvent composition in HILIC must be carefully optimized for accurate quantitative data collection and for adequate separation.
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