Namihisa T, Tamura K, Saifuku K, Imanari H, Kuroda H, Kanaoka Y, Okamoto Y, Sekine T
J Histochem Cytochem. 1980 Apr;28(4):335-8. doi: 10.1177/28.4.6989895.
For fluorescent staining of microfilaments in cells, heavy meromyosin (HMM) or subfragment-1 (S-1) was labeled with a novel thiol-directed fluorescent dye, N-(7-dimethylamino-4-methylcoumarinyl) maleimide (DACM), instead of the usual dyes, such as fluorescein-isothiocyanate (FITC). DACM-labeled HMM or S-1 gave characteristic fluorescence patterns to a variety of cell types similar to those reported with the use of FITC-labeled HMM or S-1 or with immunofluorescence techniques using anti-actin antibody. The fluorescence of DACM was fairly photoresistant as compared with FITC, so that HMM or S-1 required only 1 mol of the dye per myosin head. Consequently, F-actin need not be used to preserve the actin binding activity of the myosin fragments when labeling with the dye.
对于细胞中微丝的荧光染色,用一种新型的硫醇导向荧光染料N-(7-二甲基氨基-4-甲基香豆素基)马来酰亚胺(DACM)标记重酶解肌球蛋白(HMM)或亚片段-1(S-1),而不是常用的染料,如异硫氰酸荧光素(FITC)。用DACM标记的HMM或S-1对多种细胞类型呈现出特征性的荧光模式,类似于使用FITC标记的HMM或S-1或使用抗肌动蛋白抗体的免疫荧光技术所报道的模式。与FITC相比,DACM的荧光具有相当强的抗光性,因此HMM或S-1每个肌球蛋白头部仅需1摩尔染料。因此,在用该染料标记时,无需使用F-肌动蛋白来保持肌球蛋白片段的肌动蛋白结合活性。