Enrichment of Glycoproteins using Nanoscale Chelating Concanavalin A Monolithic Capillary Chromatography

被引:78
作者
Feng, Shun [1 ]
Yang, Na [1 ]
Pennathur, Subramaniam [2 ]
Goodison, Steve [3 ]
Lubman, David M. [1 ,4 ,5 ]
机构
[1] Univ Michigan, Dept Surg, Med Ctr, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Div Nephrol, Ann Arbor, MI 48109 USA
[3] Univ Florida, Dept Surg, Jacksonville, FL 32009 USA
[4] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[5] Univ Michigan, Med Ctr, Ctr Comprehens Canc, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
LECTIN AFFINITY-CHROMATOGRAPHY; N-LINKED GLYCOPROTEINS; MASS-SPECTROMETRY; PHOSPHOPROTEOME ANALYSIS; PLASMA GLYCOPROTEINS; PROTEIN DIGESTION; BLADDER-CANCER; IDENTIFICATION; ELECTROPHORESIS; GLYCOSYLATION;
D O I
10.1021/ac900085k
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
Immobilized lectin chromatography can be employed for glycoprotein enrichment, but commonly used columns have limitations of yield and resolution. To improve efficiency and to make the technique applicable to minimal sample material, we have developed a nanoscale chelating Concanavalin A (Con A) monolithic capillary prepared using GMA-EDMA (glycidyl methacrylate-co-ethylene dimethacrylate) as polymeric support. Con A was immobilized on Cu(II)-charged iminodiacetic acid (IDA) regenerable sorbents by forming a IDA.-Cu(II):Con A sandwich affinity structure that has high column capacity, as well as stability. When compared with conventional Con A lectin chromatography, the monolithic capillary enabled the better reproducible detection of over double the number of unique N-glycoproteins in human urine samples. Utility for analysis of minimal biological samples was confirmed by the successful elucidation of glycoprotein profiles in mouse urine samples at the microliter scale. The improved efficiency of the nanoscale monolithic capillary will impact the analysis of glycoproteins in complex biological samples, especially where only limited material may be available.
引用
收藏
页码:3776 / 3783
页数:8
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