Robson DNA Science Centre, Arnie Charbonneau Cancer Institute, and Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, 3330 Hospital Drive NW, Calgary, AB T2N 4N1, Canada.
Robson DNA Science Centre, Arnie Charbonneau Cancer Institute, and Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, 3330 Hospital Drive NW, Calgary, AB T2N 4N1, Canada.
DNA Repair (Amst). 2023 Sep;129:103545. doi: 10.1016/j.dnarep.2023.103545. Epub 2023 Jul 27.
Laser microirradiation coupled with live-cell fluorescence microscopy is a powerful technique that has been used widely in studying the recruitment and retention of proteins at sites of DNA damage. Results obtained from this technique can be found in published works by both seasoned and infrequent users of microscopy. However, like many other microscopy-based techniques, the presentation of data from laser microirradiation experiments is inconsistent; papers report a wide assortment of analytic techniques, not all of which result in accurate and/or appropriate representation of the data. In addition to the varied methods of analysis, experimental and analytical details are commonly under-reported. Consequently, publications reporting data from laser microirradiation coupled with fluorescence microscopy experiments need to be carefully and critically assessed by readers. Here, we undertake a systematic investigation of commonly reported corrections used in the analysis of laser microirradiation data. We validate the critical need to correct data for photobleaching and we identify key experimental parameters that must be accounted for when presenting data from laser microirradiation experiments. Furthermore, we propose a straightforward, four-step analytical protocol that can readily be applied across platforms and that aims to improve the quality of data reporting in the DNA damage field.
激光微照射与活细胞荧光显微镜相结合是一种强大的技术,已广泛应用于研究 DNA 损伤部位蛋白质的募集和保留。该技术的结果可在经验丰富和不常使用显微镜的用户的已发表作品中找到。然而,与许多其他基于显微镜的技术一样,激光微照射实验的数据呈现方式不一致;论文报告了各种各样的分析技术,并非所有技术都能准确和/或适当地表示数据。除了分析方法的多样性外,实验和分析细节通常也未得到充分报告。因此,读者需要仔细和批判性地评估报告激光微照射与荧光显微镜实验数据的出版物。在这里,我们系统地研究了激光微照射数据分析中常用的校正方法。我们验证了对光漂白数据进行校正的重要性,并确定了在呈现激光微照射实验数据时必须考虑的关键实验参数。此外,我们提出了一个简单的、四步分析方案,该方案可以在不同平台上轻松应用,旨在提高 DNA 损伤领域数据报告的质量。