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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >A comparison of nano-electrospray gas-phase electrophoretic mobility macromolecular analysis and matrix-assisted laser desorption/ionization linear time-of-flight mass spectrometry for the characterization of the recombinant coagulation glycoprotein von Willebrand factor
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A comparison of nano-electrospray gas-phase electrophoretic mobility macromolecular analysis and matrix-assisted laser desorption/ionization linear time-of-flight mass spectrometry for the characterization of the recombinant coagulation glycoprotein von Willebrand factor

机译:纳米电喷雾气相电泳迁移率大分子分析与基质辅助激光解吸/电离线性飞行时间质谱的比较,用于表征重组凝血糖蛋白von Willebrand因子

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摘要

Von Willebrand factor (VWF), an adhesive glycoprotein with an approximate molecular weight (MW) of the monomer of 260 kDa, circulates in human blood plasma as a series of multimers ranging in size up to 20.000 kDa; thus the determination of the accurate MW of the monomer is of great importance and due to its high MW quite challenging. In this study accurate MW determination of intact recombinant VWF monomer (rVWF) was performed with GEMMA (gas-phase electrophoretic mobility macromolecular analysis) and MALDI TOF MS(matrix-assisted laser desorption/ionization linear time-of-flight mass spectrometry). Three rVWF preparations with differing buffer systems and glycoprotein concentrations were analyzed. First investigations directed towards heterogeneity determination by means of capillary gel electrophoresis (CGE)-on-the-chip with a laser-induced fluorescence detector revealed two compounds (MW of 277 kDa (migration time 44.3 s) and 341 kDa (migration time 49.5 s)) present in each sample to varying extents, namely mature and pro-rVWF. MALDI MS analysis in the linear positive ion mode allowed the detection of mature rVWF with an exact MW of 256.1 kDa (W0.8%) and pro-rVWF with a MW of 349.8 kDa (W0.8%). Two samples containing pro-rVWF in very minor concentration resulted inGEMMAdetection of the mature rVWF with aMWof 227.4 kDa (W2.5%), derived from the measured globular size of 10.9 nm. For one sample containing both rVWF species in almost equal concentrations no differentiation of the two species was possible with GEMMA. Due to its lower resolution only a peak representing a mixture of both species at 11.8nm could be observed, yielding a MW of 298.8 kDa (W1.6%).
机译:Von Willebrand因子(VWF)是一种单体分子的近似分子量(MW)为260 kDa的黏附糖蛋白,在人体血浆中以一系列大小不超过20.000 kDa的多聚体形式循环;因此,准确测定单体的MW非常重要,并且由于其高MW颇具挑战性。在这项研究中,使用GEMMA(气相电泳迁移率大分子分析)和MALDI TOF MS(基质辅助激光解吸/电离线性飞行时间质谱)对完整重组VWF单体(rVWF)进行了准确的MW测定。分析了三种具有不同缓冲系统和糖蛋白浓度的rVWF制剂。最初的研究是通过带有激光诱导荧光检测器的芯片上毛细管凝胶电泳(CGE)芯片上的异质性确定的,发现了两种化合物(分子量为277 kDa(迁移时间44.3 s)和341 kDa(迁移时间49.5 s)。 ))存在于每个样品中的程度不同,即成熟和pro-rVWF。线性正离子模式下的MALDI MS分析可检测到准确的MW为256.1 kDa(W0.8%)的成熟rVWF和MW为349.8 kDa(W0.8%)的pro-rVWF。包含浓度极低的pro-rVWF的两个样品导致了测得的球状尺寸为10.9 nm的GEMMA检测到具有227.4 kDa(W2.5%)的mMW的成熟rVWF。对于一个包含几乎相同浓度的两种rVWF物种的样品,GEMMA不可能区分这两种物种。由于其较低的分辨率,只能观察到代表两种物质在11.8nm处混合的峰,产生的MW为298.8 kDa(W1.6%)。

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