质粒内基因DNA单分子计数标准物质的研制。

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Da-Hye Lee, Hee-Bong Yoo, Kee-Suk Hong, Sang-Ryoul Park, Sangkyun Jeong, Inchul Yang
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引用次数: 0

摘要

测量物质量的国际单位制单位摩尔被重新定义为固定数量的实体。这个定义可以通过计数单个实体来直接量化物质。事实证明,计数对DNA、蛋白质、病毒和细胞等大型和离散的生物实体的量化特别有效,这些生物实体很难通过传统的物理或化学方法进行量化。在这项研究中,我们详细介绍了我们开发通过单分子计数认证的基因参比物质的方法,这使得鼹鼠可追踪的测量成为可能。通过单分子计数,我们量化了三种质粒DNA结构,每种结构都携带一个特定的感兴趣基因。结果通过数字PCR和LC-MS交叉验证。通过单分子实时测序对标准物质中的序列杂质进行定量,通过双色数字PCR分析对片段杂质进行定量。在估计标准物质的总不确定度时,我们精确地考虑了各种不确定度的来源,包括测量精度、称重、均匀性和杂质。总之,本研究开发并实现了基于基因的DNA标准物质的实用格式、实现计量溯源的测量方法以及片段和序列杂质的定量方法。我们期望我们的基因DNA参考物质将作为有价值的高阶标准,用于各种生物分析应用中DNA定量的其他方法或参考物质的校准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of gene-in-plasmid DNA reference materials certified by single-molecule counting

The mole, the SI unit for measuring the amount of a substance, was redefined as a fixed number of entities. This definition enables straightforward quantification of substances by counting individual entities. Counting proves particularly effective for quantifying large and discrete biological entities such as DNA, proteins, viruses, and cells, which are challenging to quantify via traditional physical or chemical methods. In this study, we detail our approach to develop gene reference materials certified through single-molecule counting, which enables mole-traceable measurements. We quantified three plasmid DNA constructs, each carrying a specific gene of interest, via single-molecule counting. The resulting values were cross-validated via digital PCR and LC‒MS. Sequence impurities in the certified reference materials were quantified via single-molecule real-time sequencing, whereas fragment impurities were quantified via two-color digital PCR analysis. We precisely accounted for various sources of uncertainty, including measurement precision, weighing, homogeneity, and impurities, when estimating the total uncertainty of the reference materials. In conclusion, a practical format for gene-based DNA reference materials, a measurement method to achieve metrological traceability, and methods for quantifying fragments and sequence impurities were developed and implemented in this study. We anticipate that our gene-based DNA reference materials will serve as valuable higher-order standards for the calibration of other methods or reference materials for DNA quantification in a variety of bioanalytical applications.

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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
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