National Metrology Institute of Japan (NMIJ), National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Umezono, Tsukuba, Ibaraki, 305-8563, Japan.
Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8566, Japan.
Anal Bioanal Chem. 2019 Sep;411(23):6091-6100. doi: 10.1007/s00216-019-01992-y. Epub 2019 Jul 9.
Two 600-bp DNA solutions (DNA600-G and DNA600-T) were developed as certified reference material, NMIJ CRM 6205-a, for the validation of DNA quantification methods. Both DNA600-G and DNA600-T are ideal as "spike-in control" because these materials have artificial nucleic acid sequences. The certified values were determined as the mass concentration of total DNA (whole DNA materials in sample solution regardless of sequence) at 25 °C by formic acid hydrolysis/liquid chromatography-isotope dilution mass spectrometry (LC-IDMS) and inductively coupled plasma-mass spectrometry (ICP-MS) based on the amount of phosphorus. DNAs were synthesized, and plasmids including the synthesized DNAs were cloned into Escherichia coli DH5α. The amplified plasmids were digested with a restriction enzyme and highly purified. Then, the purified DNAs were diluted with water to approximately 1 ng/μL. By using the CRM-validated methods in fields where DNA quantification is required, the reliability of DNA quantification could be improved. Graphical abstract.
两段 600-bp DNA 溶液(DNA600-G 和 DNA600-T)被开发为认证参考物质,日本国家计量研究院认证参考物质 6205-a,用于验证 DNA 定量方法。由于这些材料具有人工核酸序列,因此 DNA600-G 和 DNA600-T 都是理想的“加标对照”。通过甲酸水解/液相色谱-同位素稀释质谱法(LC-IDMS)和基于磷含量的电感耦合等离子体质谱法(ICP-MS),在 25°C 下,将这两种材料的总 DNA(样品溶液中无论序列如何的全 DNA 材料)的质量浓度确定为认证值。DNA 被合成,并将包括合成 DNA 的质粒克隆到大肠杆菌 DH5α 中。用限制性内切酶消化扩增的质粒,并进行高度纯化。然后,将纯化的 DNA 用去离子水稀释至约 1ng/μL。通过在需要进行 DNA 定量的领域中使用经过 CRM 验证的方法,可以提高 DNA 定量的可靠性。