Petschel K, Naujok A, Kempter P, Seiffert W, Zimmermann H W
Histochemistry. 1984;80(4):311-21. doi: 10.1007/BF00495410.
Three new acridine dyes, 3-dimethylamino-6-methoxyacridine 1, 3-amino-6-methoxyacridine 2 and 3-amino-7-methoxyacridine 3, have been prepared and tested as fluorochromes of LM- and HeLa-cells. The dyes are basic compounds (pKA: 1 8,76; 2 8,01; 3 7,65) and form cations in neutral or acidic aqueous solutions by addition of a proton to the aza-nitrogen atom of the heterocycle. The fluorochromes stain fixed LM- and HeLa-cells at pH = 6. The fluorescence shows metachromasy similar to the staining with acridine orange AO according to the technique of Bertalanffy. But there is less fading of the fluorescence. The dye 1 is the most suitable fluorochrome of the series. It was studied in detail. Using optimized staining conditions the fluorescence of the nucleus is yellow-green that of the cytoplasm and the nucleoli orange or brownish-red. Enzymatic digestion experiments show that the dye cations are bound to DNA in the nucleus and to RNA in the cytoplasm or nucleoli. The absorption and emission spectra of the stained cells have been studied by means of microspectrophotometry. The absorption spectra of the nucleus and the cytoplasm are very similar. The maximum of the long wave length absorption of both occurs at 21400 cm-1 (467 nm) with a shoulder at ca 20100 cm-1 (498 nm). The fluorescence spectra of nucleus and cytoplasm of metachromatically stained cells are different. The emission maximum of the cytoplasm and nucleoli, 16200 cm-1 (617 nm), is red-shifted relative to the maximum of the nucleus, 18200 cm-1 (549 nm). This shift causes the metachromatic fluorescence effect. In addition we studied the concentration dependence of the absorption and fluorescence spectra of the cation 1 in aqueous solution, pH = 6, in the concentration range 6 X 10(-6)-6 X 10(-4) M. Shape and maximum of the long wave length absorption and emission depend only slightly on the concentration: Mean value of absorption maximum ca 21500 cm-1 (465 nm), shoulder at ca 20300 cm-1 (493 nm), fluorescence maximum ca 18300 cm-1 (547 nm). With growing concentration diminishes the molar absorptivity. This decrease in absorptivity and isosbestic points in the absorption spectra indicate the formation of dimers with growing dye concentration. The absorption spectra of the metachromatically stained cells and of the dye in aqueous solution are very similar.(ABSTRACT TRUNCATED AT 400 WORDS)
已制备出三种新型吖啶染料,即3 - 二甲基氨基 - 6 - 甲氧基吖啶1、3 - 氨基 - 6 - 甲氧基吖啶2和3 - 氨基 - 7 - 甲氧基吖啶3,并将其作为荧光染料用于对LM细胞和HeLa细胞进行染色测试。这些染料为碱性化合物(pKA:1 8.76;2 8.01;3 7.65),在中性或酸性水溶液中,通过向杂环的氮杂原子上加一个质子形成阳离子。这些荧光染料在pH = 6时对固定的LM细胞和HeLa细胞进行染色。其荧光显示出与根据贝塔朗菲技术用吖啶橙AO染色相似的异染性。但荧光的褪色较少。染料1是该系列中最合适的荧光染料。对其进行了详细研究。在优化的染色条件下,细胞核的荧光为黄绿色,细胞质和核仁的荧光为橙色或棕红色。酶消化实验表明,染料阳离子与细胞核中的DNA以及细胞质或核仁中的RNA结合。已通过显微分光光度法研究了染色细胞的吸收光谱和发射光谱。细胞核和细胞质的吸收光谱非常相似。两者长波吸收的最大值均出现在21400 cm-1(467 nm)处,在约20100 cm-1(498 nm)处有一个肩峰。异染性染色细胞的细胞核和细胞质的荧光光谱不同。细胞质和核仁的发射最大值16200 cm-1(617 nm)相对于细胞核的最大值18200 cm-1(549 nm)发生红移。这种红移导致了异染性荧光效应。此外,我们研究了在pH = 6的水溶液中,阳离子1在6×10(-6)-6×10(-4) M浓度范围内吸收光谱和荧光光谱的浓度依赖性。长波吸收和发射的形状及最大值仅略微依赖于浓度:吸收最大值的平均值约为21500 cm-1(465 nm),在约20300 cm-1(493 nm)处有肩峰,荧光最大值约为18300 cm-1(547 nm)。随着浓度增加,摩尔吸光率降低。这种吸光率的降低以及吸收光谱中的等吸收点表明随着染料浓度增加会形成二聚体。异染性染色细胞的吸收光谱与染料在水溶液中的吸收光谱非常相似。(摘要截于400字)