Analytical Scheme Leading to Integrated High-Sensitivity Profiling of Glycosphingolipids Together with N- and O-Glycans from One Sample

被引:9
|
作者
Benktander, John D. [1 ]
Gizaw, Solomon T. [1 ]
Gaunitz, Stefan [1 ]
Novotny, Milos V. [1 ]
机构
[1] Indiana Univ, Dept Chem, 800 E Kirkwood Ave, Bloomington, IN 47405 USA
关键词
Integrated glycomic scheme; N- and O-glycans; Glycosphingolipid (GSL) glycans; SIALIC-ACID DERIVATIZATION; OVARIAN-CANCER PATIENTS; MASS-SPECTROMETRY; COLORECTAL-CANCER; LINKED GLYCANS; STRUCTURAL-CHARACTERIZATION; PROTEIN GLYCOSYLATION; BIOMARKER DISCOVERY; SERUM; IDENTIFICATION;
D O I
10.1007/s13361-018-1933-y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Glycoconjugates are directly or indirectly involved in many biological processes. Due to their complex structures, the structural elucidation of glycans and the exploration of their role in biological systems have been challenging. Glycan pools generated through release from glycoprotein or glycolipid mixtures can often be very complex. For the sake of procedural simplicity, many glycan profiling studies choose to concentrate on a single class of glycoconjugates. In this paper, we demonstrate it feasible to cover glycosphingolipids, N-glycans, and O-glycans isolated from the same sample. Small volumes of human blood serum and ascites fluid as well as small mouse brain tissue samples are sufficient to profile sequentially glycans from all three classes of glycoconjugates and even positively identify some mixture components through MALDI-MS and LC-ESI-MS. The results show that comprehensive glycan profiles can be obtained from the equivalent of 500-mu g protein starting material or possibly less. These methodological improvements can help accelerating future glycomic comprehensive studies, especially for precious clinical samples.
引用
收藏
页码:1125 / 1137
页数:13
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