Reimer G, Leonhardi G, Schwulera V
Arch Dermatol Res (1975). 1977 Oct 27;260(1):39-46. doi: 10.1007/BF00558012.
DNA binding proteins (DBP) are shown to be engaged in the regulatory functions of the genome. Since the accelerated epidermopoesis in psoriasis indicates changed gene activities, the examination of DBP possible could help to clarify the pathological processes. Psoriatic scales were used to elaborate the method. DBP was isolated from a protein extract by affinity chromatography with DNA-cellulose according to Alberts et al. About 3-5% of postribosomal crude protein (PCP) extract had an affinity to DNA. The separation of DBP on SDS polyacrylamide slab gels showed a characteristic spectrum of proteins with molecular weights from 12.7 to 150 X 10(3) daltons. The protein band spectrum of the concentrated DBP fraction was different from that of the crude extract. These observations show the isolated DBP to represent an own group of water soluble proteins with DNA binding abilities.
已表明DNA结合蛋白(DBP)参与基因组的调节功能。由于银屑病中表皮生成加速表明基因活性发生了变化,因此检测DBP可能有助于阐明病理过程。采用银屑病鳞屑来完善该方法。根据阿尔伯茨等人的方法,通过用DNA纤维素进行亲和色谱从蛋白质提取物中分离出DBP。约3 - 5%的核糖体后粗蛋白(PCP)提取物对DNA具有亲和力。在SDS聚丙烯酰胺平板凝胶上分离DBP显示出分子量从12.7至150×10³道尔顿的特征性蛋白质谱。浓缩的DBP组分的蛋白带谱与粗提取物的不同。这些观察结果表明分离出的DBP代表了一组具有DNA结合能力的自身水溶性蛋白质。