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Matrix-assisted laser desorption/ionization mass spectrometry for the analysis of polyamines in plant micro-tissues using cucurbituril as a host molecule

机译:基质辅助激光解吸/电离质谱分析植物微观组织中的多胺,用CUCUBRITIL作为宿主分子

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In this study, a matrix-assisted laser desorption/ionization (MALDI) mass spectrometry (MS) strategy using cucurbit[n]uril (CB[n]) as a host molecule is proposed for the analysis of low molecular weight (LMW) compounds in complex samples. As a proof-of-concept, CB[6] was selected as the host molecule, and endogenous polyamines in plant tissue were chosen as the target analytes. Due to the molecular recognition and mass shifting properties of CB[6], the ionic signals associated with polyamines were moved to the higher mass region (>1000 Da) after specifically binding to CB[6], while signal interference derived from the conventional organic matrix and the complex sample matrix remained in the low mass region because of the incompatibility of their molecular size with CB[6] cavities. The strategy not only facilitated the analysis of LMW compounds in complex samples by MALDI MS, but also offered high throughput by accomplishing the entire analytical procedure within 10 min. The detection of polyamine concentration showed good linearity in the range of 0.02-10.0 ng/mL with correlation coefficients (R) greater than 0.9915. The limits of detection were 8.8-28.8 pg. The good reproducibility and reliability of the method were demonstrated by excellent intraday and interday precisions with relative standard deviations less than 7.9%, and the recovery ranged from 92.1% to 117.1%. Finally, the good sensitivity of the method allowed for the quantitative analysis of endogenous polyamine concentrations in various microtissues of Arabidopsis thaliana (20.0-740.0 mg fresh weight for each sample). (C) 2017 Elsevier B.V. All rights reserved.
机译:在该研究中,提出了使用葫芦(CB [N] URIL(CB [N])作为宿主分子的基质辅助激光解吸/电离(MAS)策略用于分析低分子量(LMW)化合物在复杂的样品中。作为概念验证,选择CB [6]作为宿主分子,选择植物组织中的内源多胺作为靶分析物。由于CB [6]的分子识别和质量换档性能,在特异性结合CB [6]之后,与多胺相关的离子信号移动到较高质量区域(> 1000DA),而来自常规有机的信号干扰由于其分子大小与CB [6]空腔的不相容性,基质和复杂样品基质仍然存在于低质量区域中。该策略不仅促进了MALDI MS在复杂样品中的LMW化合物分析,而且还通过在10分钟内完成整个分析程序提供高吞吐量。多胺浓度的检测显示在0.02-10.0ng / ml的范围内的良好线性,具有大于0.9915的相关系数(R)。检测限为8.8-28.8 pg。该方法的良好再现性和可靠性是通过具有相对标准偏差的优异的盘中和白天精度来证明,相对标准偏差小于7.9%,恢复的速度范围为92.1%至117.1%。最后,允许该方法的良好敏感性允许在拟南芥的各种微训练中的内源性多胺浓度进行定量分析(每个样品的20.0-740.0mg鲜重)。 (c)2017 Elsevier B.v.保留所有权利。

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