Flanagan S D, Yost B, Crawford G
J Cell Biol. 1982 Sep;94(3):743-8. doi: 10.1083/jcb.94.3.743.
Cerebrum and cerebellum contain numerous asymmetric synapses characterized by the presence of a postsynaptic thickening prominently stained by phosphotungstic acid and other electron-dense stains suitable for electron microscopy. A 51,000-Mr protein, copurified in postsynaptic density-enriched fractions from cerebrum, is considered to be a well established marker for the postsynaptic density. On the basis of two criteria, our studies demonstrate that the 51,000-Mr protein marker for postsynaptic densities is virtually absent in cerebellum, First, it is present in negligible amounts in deoxycholate-insoluble fractions from cerebellum but abundant in parallel fractions from cerebrum. Secondly, the 51,000-Mr protein, which binds 125I-calmodulin after SDS PAGE is readily visualized in membrane samples from cerebrum but is virtually undetectable in cerebellar samples. It is apparent that these results require reexamination of the role of the 51,000-Mr protein in postsynaptic density structures.
大脑和小脑含有大量不对称突触,其特征是存在突触后增厚,用磷钨酸和其他适合电子显微镜的电子致密染色剂可显著染色。一种51000道尔顿的蛋白质,从大脑中富含突触后致密物的组分中共同纯化得到,被认为是突触后致密物的一个公认标志物。基于两个标准,我们的研究表明,小脑几乎不存在用于突触后致密物的51000道尔顿蛋白质标志物。首先,它在小脑的脱氧胆酸盐不溶组分中的含量微不足道,但在大脑的平行组分中含量丰富。其次,在十二烷基硫酸钠聚丙烯酰胺凝胶电泳后能结合125I-钙调蛋白的51000道尔顿蛋白质,在大脑的膜样品中很容易观察到,但在小脑样品中几乎检测不到。显然,这些结果需要重新审视51000道尔顿蛋白质在突触后致密结构中的作用。