High UV Excitation Intensity Induces Photoconversion of DAPI During Wide-Field Microscopy

C. Brown
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Abstract

Background: Multi-color fluorescence microscopy is dependent on the spectral specificity of the dyes and probes used for localization. One of the most commonly used fluorescent DNA dyes is DAPI, which is usually excited by UV light to emit in the blue visible light range. Herein, we describe a pattern of decreasing DAPI fluorescence upon extended UV exposure, closely followed by an increase in emission maxima in the green range. Methods: UV-induced photo-conversion of DAPI to green-fluorescing photoproducts was studied on Chinese hamster ovary cells using wide-field fluorescence microscopy, at different UV exposure times and intensities. Imaging was done in repetitive cycles, by alternating between a DAPI and FITC filter cube and following this with a 1 second UV excitation time. The effect of differing UV light intensities on the photo- conversion process was not previously described in the literature. Results: Upon image analysis from a large sample of cells, the rate of photo-conversion was shown to be dependent on both the duration of UV excitation and the intensity of the UV light source. Both the process of DAPI depletion and photo-product growth showed biphasic exponential patterns of change. Furthermore, the level of DAPI fluorescence intensity was found to be negatively correlated with the green fluorescence of the photo-product. Limitations: This study did not examine the effect of differing mounting media or a variation in DAPI concentration on the rate of DAPI photo-conversion. Also, the exact light dosage to the system was not measured from the 100W Hg bulb. Photo-bleaching of green fluorescence in cells not stained with DAPI was not measured to control for bleaching of endogenous cell molecules. Conclusion: Based on our findings, a set of recommendations was formulated in order to help reduce the effects of UV-induced DAPI photo-conversion.
高紫外激发强度诱导DAPI在宽视场显微镜下的光转换
背景:多色荧光显微镜依赖于用于定位的染料和探针的光谱特异性。最常用的荧光DNA染料之一是DAPI,它通常被紫外光激发,在蓝色可见光范围内发射。在这里,我们描述了一种模式,减少DAPI荧光在延长紫外线照射,紧随其后的是在绿色范围内的发射最大值的增加。方法:利用宽视场荧光显微镜研究了不同紫外照射时间和强度下,DAPI在中国仓鼠卵巢细胞中转化为绿色荧光产物。通过在DAPI和FITC滤光片立方体之间交替进行重复循环成像,然后进行1秒的紫外线激发时间。不同紫外光强度对光转化过程的影响在以前的文献中没有描述过。结果:通过对大量细胞样本的图像分析,显示出光转换速率取决于紫外线激发的持续时间和紫外线光源的强度。DAPI耗竭和光产物生长过程均呈双相指数型变化。此外,DAPI的荧光强度水平与光产物的绿色荧光呈负相关。局限性:本研究没有检查不同的安装介质或DAPI浓度变化对DAPI光转化率的影响。此外,系统的确切光剂量不是从100W Hg灯泡测量的。未检测DAPI染色细胞中绿色荧光的光漂白,以控制内源性细胞分子的漂白。结论:基于我们的研究结果,提出了一套建议,以帮助减少紫外线诱导的DAPI光转化的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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