Reidl L S, Campagnoni C W, Campagnoni A T
J Neurochem. 1981 Aug;37(2):373-80. doi: 10.1111/j.1471-4159.1981.tb00465.x.
An immunosorbent column specific for the myelin basic protein (BP) was prepared by coupling purified anti-BP antibodies to cyanogen bromide (BrCN)-activated Sepharose 4B. The BP-immunosorbent column bound BP between pH 4.5 and pH 6.8. In its working range the column bound approximately 400-475 microgram of BP at pH 6.8 and 250 microgram at pH 4.5 with recoveries of 72-77%. The BP-immunosorbent column could effectively separate BP from simple mixtures of BP and proteins of similar size and charge and from acid extracts of bovine brain. The results indicate that the BP-immunosorbent column can be used to isolate BP from a mixture of proteins and may be adapted for use in the small-scale purification of the myelin basic proteins involving a minimum number of steps.
通过将纯化的抗髓鞘碱性蛋白(BP)抗体偶联到溴化氰(BrCN)活化的琼脂糖凝胶4B上,制备了一种对髓鞘碱性蛋白具有特异性的免疫吸附柱。BP免疫吸附柱在pH 4.5至pH 6.8之间结合BP。在其工作范围内,该柱在pH 6.8时结合约400 - 475微克的BP,在pH 4.5时结合250微克,回收率为72 - 77%。BP免疫吸附柱可以有效地从BP与大小和电荷相似的蛋白质的简单混合物以及牛脑酸提取物中分离出BP。结果表明,BP免疫吸附柱可用于从蛋白质混合物中分离BP,并可适用于涉及最少步骤的髓鞘碱性蛋白的小规模纯化。