Nöhammer G, Khoschsorur G
Microsc Acta. 1981 Sep;85(1):19-24.
The total protein and total protein-SH content of both the cytoplasmic fraction and the nuclei of Ehrlich ascites tumor cells (EATC) were determined macroscopically and microspectrometrically. The separation into cytoplasmic and nuclear fraction was performed by a modification of the method of Mamaril et al. [4]. The macroscopical determination of the total protein and the total protein-SH content were performed with the Folin method of Lowry et al. [2] and the DTNB method of Ellman [1], respectively. The quantitative microspectrometrical determinations of total protein content and of total protein-SH content were performed using the tetrazonium staining method of Nöhammer [5] and Nöhammer et al. [6] and the mercurochromcyanide (MCN) method of Nöhammer et al. [7], respectively. Within the intact cells, fixed and stained histochemically, the total protein and the total protein-SH content of the nuclei were determined microspectrometrically. The so called "nuclear extinctions", measured as the sum of the extinctions of the nucleus and of the parts of the cytoplasm above and below the nucleus, were calculated into the true nuclear extinctions, which then show a good correspondence to the values measured both microspectrometrically and macroscopically on isolated nuclei. The calculation for the true nuclear extinctions is based on a special preparation of spherically shaped cells and nuclei.
采用宏观和微量光谱法测定了艾氏腹水瘤细胞(EATC)细胞质组分和细胞核中的总蛋白及总蛋白-SH含量。细胞质和细胞核组分的分离是对Mamaril等人[4]的方法进行改良后进行的。总蛋白和总蛋白-SH含量的宏观测定分别采用Lowry等人[2]的Folin法和Ellman[1]的DTNB法。总蛋白含量和总蛋白-SH含量的定量微量光谱测定分别采用Nöhammer[5]和Nöhammer等人[6]的四唑染色法以及Nöhammer等人[7]的汞氰化铬(MCN)法。在完整细胞内,经过组织化学固定和染色后,采用微量光谱法测定细胞核中的总蛋白和总蛋白-SH含量。将所谓的“核消光值”(以细胞核以及细胞核上方和下方细胞质部分的消光值总和来衡量)换算为真实的核消光值,其与对分离出的细胞核进行微量光谱测定和宏观测定所得的值具有良好的对应关系。真实核消光值的计算基于对球形细胞和细胞核的特殊制备方法。