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一种用户友好、高通量的工具,可精确荧光定量生物样品中的脱氧核苷三磷酸。

A user-friendly, high-throughput tool for the precise fluorescent quantification of deoxyribonucleoside triphosphates from biological samples.

机构信息

Institute of Enzymology, Research Centre for Natural Sciences, Budapest 1117, Hungary.

Department of Applied Biotechnology and Food Sciences, Budapest University of Technology and Economics, Budapest 1111, Hungary.

出版信息

Nucleic Acids Res. 2020 May 7;48(8):e45. doi: 10.1093/nar/gkaa116.

Abstract

Cells maintain a fine-tuned, dynamic concentration balance in the pool of deoxyribonucleoside 5'-triphosphates (dNTPs). This balance is essential for physiological processes including cell cycle control or antiviral defense. Its perturbation results in increased mutation frequencies, replication arrest and may promote cancer development. An easily accessible and relatively high-throughput method would greatly accelerate the exploration of the diversified consequences of dNTP imbalances. The dNTP incorporation based, fluorescent TaqMan-like assay published by Wilson et al. has the aforementioned advantages over mass spectrometry, radioactive or chromatography based dNTP quantification methods. Nevertheless, the assay failed to produce reliable data in several biological samples. Therefore, we applied enzyme kinetics analysis on the fluorescent dNTP incorporation curves and found that the Taq polymerase exhibits a dNTP independent exonuclease activity that decouples signal generation from dNTP incorporation. Furthermore, we found that both polymerization and exonuclease activities are unpredictably inhibited by the sample matrix. To resolve these issues, we established a kinetics based data analysis method which identifies the signal generated by dNTP incorporation. We automated the analysis process in the nucleoTIDY software which enables even the inexperienced user to calculate the final and accurate dNTP amounts in a 96-well-plate setup within minutes.

摘要

细胞在脱氧核苷 5'-三磷酸(dNTP)池维持着精细、动态的浓度平衡。这种平衡对于包括细胞周期控制或抗病毒防御在内的生理过程至关重要。其扰动会导致突变频率增加、复制停滞,并可能促进癌症发展。一种易于获取且相对高通量的方法将极大地加速对 dNTP 失衡多样化后果的探索。Wilson 等人发表的基于 dNTP 掺入的荧光 TaqMan 样测定法具有上述优于质谱、放射性或基于色谱的 dNTP 定量方法的优点。然而,该测定法在几个生物样本中未能产生可靠的数据。因此,我们对荧光 dNTP 掺入曲线进行了酶动力学分析,发现 Taq 聚合酶表现出与 dNTP 掺入无关的外切核酸酶活性,从而将信号产生与 dNTP 掺入分离。此外,我们发现聚合酶和外切核酸酶活性都不可预测地被样品基质抑制。为了解决这些问题,我们建立了一种基于动力学的数据分析方法,该方法可以识别由 dNTP 掺入产生的信号。我们在 nucleoTIDY 软件中自动化了分析过程,即使是没有经验的用户也可以在几分钟内计算出 96 孔板设置中最终和准确的 dNTP 量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b5c/7192609/51be0261b9d2/gkaa116fig1.jpg

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