Gilbert W R, Garwood M M, Agrawal D, Schmidt R E, Agrawal H C
Neurochem Res. 1982 Dec;7(12):1495-506. doi: 10.1007/BF00965092.
The immunoblot technique permits the visualization of proteins following their separation on acrylamide gels, transfer to cellulose nitrate sheets and subsequent staining with antiserum. We have utilized this technique to demonstrate the presence of four basic proteins in rat PNS myelin with molecular weights of 21K, 18K, 17K, and 14K. Similarly, we demonstrated the presence of two basic proteins in rabbit PNS myelin (molecular weights of 21K and 18K). Exposure of the immunostained cellulose nitrate strips to X-ray film revealed the phosphorylation of four and two basic proteins in rat and rabbit PNS myelin, respectively. These basic proteins were present in the CNS myelin of the two species and were also phosphorylated. Because of the sensitivity of the immunoblot technique, it was also possible for us to visualize the P2 protein in both rat and rabbit PNS myelin.
免疫印迹技术可使蛋白质在丙烯酰胺凝胶上分离、转移至硝酸纤维素膜上,随后用抗血清染色后得以可视化。我们利用该技术证实了大鼠周围神经系统髓鞘中存在四种碱性蛋白,其分子量分别为21K、18K、17K和14K。同样,我们也证实在兔周围神经系统髓鞘中存在两种碱性蛋白(分子量为21K和18K)。将免疫染色的硝酸纤维素条带与X射线胶片曝光后发现,大鼠和兔周围神经系统髓鞘中分别有四种和两种碱性蛋白发生了磷酸化。这两种动物的中枢神经系统髓鞘中也存在这些碱性蛋白,并且它们也发生了磷酸化。由于免疫印迹技术的敏感性,我们还能够在大鼠和兔的周围神经系统髓鞘中观察到P2蛋白。