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首页> 外文期刊>European Biophysics Journal >INCORPORATION OF ETHIDIUM BROMIDE IN THE DROSOPHILA SALIVARY GLAND APPROACHED BY MICROSPECTROFLUOROMETRY - EVIDENCE FOR THE PRESENCE OF BOTH FREE AND BOUND DYE IN THE NUCLEI OF CELLS IN VIABLE CONDITIONS
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INCORPORATION OF ETHIDIUM BROMIDE IN THE DROSOPHILA SALIVARY GLAND APPROACHED BY MICROSPECTROFLUOROMETRY - EVIDENCE FOR THE PRESENCE OF BOTH FREE AND BOUND DYE IN THE NUCLEI OF CELLS IN VIABLE CONDITIONS

机译:微量荧光素法测定果蝇唾液腺中的溴化乙锭含量-活体条件下细胞核中存在游离染料和结合染料的证据

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The incorporation of 10(-6) M ethidium bromide (EB) was studied in viable Drosophila melanogaster salivary glands with a spatial resolution reaching a few mu m(3), using a confocal laser microspectrofluorometer designed for spectral analysis. Spectra were recorded with the 514 nm Argon laser line during excitation times of 1 second (20 mu W on the preparation) at 5 min intervals for 30 or 60 min, either at points in determined cell sites or serially throughout the cells. The fluorescence intensity time-course indicated that the EB intake was not an all-or-none process, but rather a graded, sensitive indicator of the functional state of the cell. On the micrometer scale, the cytoplasm behaved as an homogeneous substrate with the fluorescence intensity depending on EB intake and intracellular diffusion. In the nucleus? however, localized enhancement of the emission intensity was observed. Spectral analysis allowed us to characterize the interactions. The mean values of lambda(max) in the cytoplasm (600 nm), in the nucleus (601 nm) and outside the glands (602 nm) were less than for free EB in aqueous solution (630 nm); values of full width at half maximum were between 92 and 96 nm, which is much lower than the 120 nm observed for free EB. The recorded spectra were analyzed using a linear combination of two spectral models, namely free and DNA intercalated EB. In the nucleus, the free EB model spectra was found to represent up to 10% of the recorded spectra whereas it was near zero in the cytoplasm. The present data suggest that the intranuclear concentration of free EB (allowing for its lower fluorescence quantum yield) might be at least equal to that of the bound EB. [References: 63]
机译:使用专为光谱分析设计的共聚焦激光显微分光光度计,在空间分辨率达到几μm(3)的果蝇果蝇唾液腺中研究了10(-6)溴化乙锭(EB)的结合。在1秒的激发时间(制剂中为20μW)以514 nm氩激光线在5分钟的间隔内连续30或60分钟记录光谱,无论是在确定的细胞位点还是在整个细胞中连续进行。荧光强度随时间变化表明,EB摄入不是一个全过程或一个无过程,而是细胞功能状态的分级敏感指标。在微米尺度上,细胞质表现为均匀的底物,其荧光强度取决于EB摄入量和细胞内扩散。在核中?然而,观察到发射强度的局部增强。光谱分析使我们能够表征相互作用。细胞质(600 nm),细胞核(601 nm)和腺体外部(602 nm)的λ(max)平均值小于水溶液中的游离EB(630 nm);半高处的全宽值在92至96 nm之间,远低于游离EB所观察到的120 nm。使用两个光谱模型的线性组合来分析记录的光谱,这两个光谱模型分别是游离和DNA嵌入的EB。在细胞核中,发现自由EB模型光谱占记录光谱的10%,而在细胞质中接近零。目前的数据表明,游离EB的核内浓度(允许其较低的荧光量子产率)可能至少等于结合的EB的浓度。 [参考:63]

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