Smerchinskaia L S, Belik Ia V, Syrovatskaia L P, Birillo T N
Ukr Biokhim Zh. 1976 Sep-Oct;48(5):609-14.
Protein S-100 specific for the nervous system was isolated from the bull cerebral hemispheres by the Steward method and antiserum monospecific to it was obtained. In immunoelectrophoretical study of the initial brain extract with antiserum detected the paired line of precipitation consisting of two arcs in the zone of prealbumins and alpha2-globulins of the the serum, and that with purified protein fraction showed only one arc corresponding to the prealbumin component. The purified protein S-100 fraction in agar gel is divided into a series of prealbumin electrophoretic zones, with a pre-protein locating chiefly in the most mobile zone. It is established that heterogeneity of protein S-100 with electrophoresis in agar gel and immunophoresis is due to the presence of calcium ions in the systems. In the presence of 1 mM EDTA solution the one or two closely located prealbumin zones of purified protein S-100 migrates. The obtained monospecific antiserum made it possible to establish that two-fractional antigen A detected previously by the heterogenic antisera is protein S-100.
采用斯图尔德方法从公牛大脑半球中分离出对神经系统具有特异性的蛋白质S - 100,并获得了对其具有单特异性的抗血清。在用抗血清对初始脑提取物进行免疫电泳研究时,在血清的前清蛋白和α2 -球蛋白区域检测到由两条弧组成的沉淀配对线,而用纯化的蛋白质组分进行检测时,仅显示出一条对应于前清蛋白组分的弧。琼脂凝胶中的纯化蛋白质S - 100组分被分为一系列前清蛋白电泳区,前蛋白主要位于迁移最快的区域。已确定,蛋白质S - 100在琼脂凝胶电泳和免疫电泳中的异质性是由于系统中存在钙离子。在存在1 mM乙二胺四乙酸(EDTA)溶液的情况下,纯化蛋白质S - 100的一个或两个紧密相邻的前清蛋白区会发生迁移。所获得的单特异性抗血清使得能够确定先前由异源抗血清检测到的双组分抗原A是蛋白质S - 100。