Instituto de Medicina Molecular-João Lobo Antunes, Faculdade Medicina da Universidade de Lisboa, Lisbon, Portugal.
CIISA-Centro de Investigação Interdisciplinar em Sanidade Animal, Faculdade de Medicina Veterinária, Universidade de Lisboa, Lisbon, Portugal.
Methods Mol Biol. 2021;2329:165-177. doi: 10.1007/978-1-0716-1538-6_12.
The principles and practice of a methodology of cell cycle analysis that allows the estimation of the absolute length (in units of time) of all cell cycle stages (G1, S, and G2) are detailed herein. This methodology utilizes flow cytometry to take full advantage of the excellent stoichiometric properties of click chemistry. This allows detection, via azide-fluorochrome coupling, of the modified deoxynucleoside 5-ethynyl-2'-deoxyuridine (EDU) incorporated into replicated DNA through incremental pulsing times. This methodology, which we designated as EdU-Coupled Fluorescence Intensity (E-CFI) analysis, can be applied to cell types with very distinct cell cycle features, and has shown excellent agreement with established techniques of cell cycle analysis. Useful modifications to the original protocol (Pereira et al., Oncotarget, 8:40514-40,532, 2017) have been introduced to increase flexibility in data collection and facilitate data analysis.
本文详细介绍了一种细胞周期分析方法的原理和实践,该方法可以估计所有细胞周期阶段(G1、S 和 G2)的绝对长度(时间单位)。该方法利用流式细胞术充分利用点击化学的优良化学计量性质。这允许通过叠氮化物-荧光染料偶联,检测通过递增脉冲时间掺入复制 DNA 中的修饰的脱氧核苷 5-乙炔基-2'-脱氧尿苷(EDU)。我们将这种方法命名为 EdU 偶联荧光强度(E-CFI)分析,它可以应用于具有非常明显细胞周期特征的细胞类型,并且与细胞周期分析的既定技术具有很好的一致性。对原始方案(Pereira 等人,Oncotarget,8:40514-40,532,2017)进行了有用的修改,以增加数据收集的灵活性并便于数据分析。