Pollow K, Fleischer H, Pollow B
J Clin Chem Clin Biochem. 1979 Jun;17(6):379-88. doi: 10.1515/cclm.1979.17.6.379.
In the study reported here, non-histamine chromosomal proteins from proliferative and secretory human endometrium, and from undifferentiated endometrial carcinoma have been separated into more than 750 protein components, using a new preparative and highly sensitive analytical method. The following experimental procedure was applied: 1. Dissociation of chromatin under different conditions (variable parameters: ion strength, dissociation agents, shearing, pH), 2. cation exchange chromatography over Bio Rex, 3. preparative fractionation of those non-histamine chromosomal proteins which are not adsorbed on Bio Rex 70 in a Valmet-electrofocusing apparatus, 4. micro-electrophoresis of the focused proteins in microgels containing a continous gradient of polyacrylamide, 5. two-dimensional electrophoresis of the strongly basic chromosomal proteins. There are qualitative differences with respect to the components of this class of proteins between proliferative and secretory endometrium and endometrial carcinoma. The relevance of these results to the control of gene activity is discussed.
在本文报道的研究中,利用一种新的制备性且高灵敏度的分析方法,已将来自增殖期和分泌期人子宫内膜以及未分化子宫内膜癌的非组蛋白染色体蛋白分离成750多种蛋白成分。采用了以下实验步骤:1. 在不同条件下(可变参数:离子强度、解离剂、剪切、pH值)使染色质解离;2. 在Bio Rex上进行阳离子交换色谱分析;3. 在瓦尔梅特电聚焦仪中对那些未吸附在Bio Rex 70上的非组蛋白染色体蛋白进行制备性分级分离;4. 在含有连续聚丙烯酰胺梯度的微凝胶中对聚焦蛋白进行微电泳;5. 对强碱性染色体蛋白进行二维电泳。增殖期和分泌期子宫内膜以及子宫内膜癌之间,这类蛋白的成分存在质的差异。文中讨论了这些结果与基因活性控制的相关性。