Sun Xudong, Dong Jing, Li Jinan, Ye Mingliang, Zhang Weibing, Ou Junjie
Shanghai Key Laboratory of Functional Materials Chemistry, School of Chemistry & Molecular Engineering, East China University of Science and Technology, Shanghai 200237, PR China.
Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences (CAS), Dalian 116023, PR China.
J Chromatogr A. 2017 May 19;1498:72-79. doi: 10.1016/j.chroma.2016.12.045. Epub 2016 Dec 16.
A facile approach for preparation of hydrophilic polysaccharide-functionalized macroporous adsorption resin (MAR) was presented. Polydisperse MAR with approximately 250μm in diameter was synthesized via suspension polymerization and then modified with polysaccharides, sodium hyaluronate (HA) and chitosan (CS), through layer-by-layer (LbL) self-assembly process. The preparation method was facile, low cost and easy to expand production from tens of grams to one kilogram. The resulting MAR@(HA/CS) possesses highly hydrophilic property and rapid adsorption behavior. The specificity and efficiency of MAR@(HA/CS) to glycopeptide was demonstrated by trapping N-linked glycopeptide from tryptic digests of human immunoglobulin G (IgG) and horseradish peroxidase (HRP) with a homemade solid-phase extraction (SPE) column. The detection sensitivity for glycopeptide determined by MALDI-TOF MS was as low as 5 fmol for standard tryptic digest of human IgG. The enrichment recoveries were higher than 73%. Furthermore, in the analysis of real biological sample, 745 unique N-glycosylation sites in 1353 unique glycopeptides mapped to 379 N-glycosylated proteins were identified in three replicate analyses of protein sample extracted from mouse liver, showing the great potential of MAR@(HA/CS) in the enrichment and identification of low-abundance N-linked glycopeptides in complicated biological samples.
本文提出了一种制备亲水性多糖功能化大孔吸附树脂(MAR)的简便方法。通过悬浮聚合法合成了直径约为250μm的多分散MAR,然后通过层层(LbL)自组装过程用多糖、透明质酸钠(HA)和壳聚糖(CS)对其进行改性。该制备方法简便、成本低且易于从几十克扩大到一千克的生产规模。所得的MAR@(HA/CS)具有高度亲水性和快速吸附行为。通过使用自制的固相萃取(SPE)柱从人免疫球蛋白G(IgG)和辣根过氧化物酶(HRP)的胰蛋白酶消化物中捕获N-连接糖肽,证明了MAR@(HA/CS)对糖肽的特异性和效率。对于人IgG的标准胰蛋白酶消化物,通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)测定糖肽的检测灵敏度低至5 fmol。富集回收率高于73%。此外,在实际生物样品分析中,在从小鼠肝脏提取的蛋白质样品的三次重复分析中,鉴定出1353个独特糖肽中的745个独特N-糖基化位点,这些糖肽映射到379个N-糖基化蛋白,表明MAR@(HA/CS)在复杂生物样品中低丰度N-连接糖肽的富集和鉴定方面具有巨大潜力。