首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Development of a highly sensitive method for the quantitative analysis of modified nucleosides using UHPLC-UniSpray-MS/MS
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Development of a highly sensitive method for the quantitative analysis of modified nucleosides using UHPLC-UniSpray-MS/MS

机译:使用UHPLC-UNISPRAY-MS / MS进行改性核苷的定量分析的高敏感方法

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摘要

There are more than 150 types of naturally occurring modified nucleosides, which are believed to be involved in various biological processes. Recently, an ultrahigh performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UHPLC-ESI-MS/MS) technique has been developed to measure low levels of modified nucleosides. A comprehensive analysis of modified nucleosides will lead to a better understanding of intracellular ribonucleic acid modification, but this analysis requires high-sensitivity measurements. In this perspective, we established a highly sensitive and quantitative method using the newly developed ion source, UniSpray. A mass spectrometer was used with a UniSpray source in positive ion mode. Our UHPLC-UniSpray-MS/MS methodology separated and detected the four major nucleosides, 42 modified nucleosides, and dG15N5 (internal standard) in 15 min. The UniSpray method provided good correlation coefficients (>0.99) for all analyzed nucleosides, and a wide range of linearity for 35 of the 46 nucleosides. Additionally, the accuracy and precision values satisfied the criteria of <15% for higher concentrations and <20% for the lowest concentrations of all nucleosides. We also investigated whether this method could measure nucleosides in biological samples using mouse tissues and non-small cell lung cancer clinical specimens. We were able to detect 43 and 31 different modified nucleosides from mouse and clinical tissues, respectively. We also found significant differences in the levels of N6-methyl-N6-threonylcarbamoyladenosine (m6t6A), 1-methylinosine (m1I), 2'-0=O-methylcytidine (Cm), 5-carbamoylmethyluridine (ncm5U), 5-methoxycarbonylmethyl-2-thiouridine (mcm5S2U), and 5-methoxycarbonylmethy1-2'-O-methyluridine (mcm5Um) between cancerous and noncancerous tissues. In conclusion, we developed a highly sensitive methodology using UHPLC-UniSpray-MS/MS to simultaneously detect and quantify modified nucleosides, which can be used for analysis of biological samples. (C) 2021 Published by Elsevier B.V.
机译:有150多种天然存在的修饰核苷,据信参与各种生物过程。最近,一种超高效液相色谱-电喷雾串联质谱(UHPLC-ESI-MS/MS)技术被开发用于测量低水平的修饰核苷。对修饰核苷的全面分析将有助于更好地理解细胞内核糖核酸修饰,但这种分析需要高灵敏度的测量。从这个角度来看,我们使用新开发的离子源UniSpray建立了一种高度灵敏和定量的方法。质谱仪与正离子模式下的单喷雾源一起使用。我们的UHPC UniSpray MS/MS方法在15分钟内分离并检测了四个主要核苷、42个修饰核苷和dG15N5(内标)。UniSpray方法为所有分析的核苷提供了良好的相关系数(>0.99),并为46个核苷中的35个提供了广泛的线性范围。此外,准确度和精密度值满足所有核苷较高浓度<15%和最低浓度<20%的标准。我们还研究了该方法是否可以使用小鼠组织和非小细胞肺癌临床标本测量生物样本中的核苷。我们能够分别从小鼠和临床组织中检测到43和31种不同的修饰核苷。我们还发现癌组织和非癌组织中N6-甲基-N6-苏氨酸氨甲酰氨酰腺苷(m6t6A)、1-甲基肌苷(m1I)、2'-0=O-甲基胞苷(Cm)、5-氨甲酰甲基尿苷(ncm5U)、5-甲氧基羰基甲基-2-硫尿苷(mcm5S2U)和5-甲氧基羰基甲基-1-2'-O-甲基尿苷(mcm5Um)的水平存在显著差异。总之,我们开发了一种高灵敏度的方法,使用UHPLC UniSpray MS/MS同时检测和量化修饰核苷,可用于生物样品的分析。(c)2021由爱思唯尔B.V出版。

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