Vogel C W, Müller-Eberhard H J
J Immunol Methods. 1984 Oct 12;73(1):203-20. doi: 10.1016/0022-1759(84)90045-0.
A method to purify cobra venom factor (CVF) from cobra venom by sequential column chromatography is described which yields a product virtually free of phospholipase A2, a common contaminant of CVF preparations. The separation of phospholipase A2 from CVF was achieved by chromatography on Cibacron blue-agarose, a resin that tightly binds cobra venom phospholipase A2. A rapid and simple hemolytic assay for the qualitative and quantitative determination of CVF based on its ability to induce bystander lysis of erythrocytes has been devised. CVF was isolated from the venom of the Naja naja kaouthia subspecies and some of its biochemical properties and physicochemical parameters were delineated.
描述了一种通过连续柱色谱法从眼镜蛇毒液中纯化眼镜蛇毒因子(CVF)的方法,该方法得到的产物几乎不含磷脂酶A2,而磷脂酶A2是CVF制剂中常见的污染物。通过在Cibacron蓝琼脂糖上进行色谱分离实现了磷脂酶A2与CVF的分离,Cibacron蓝琼脂糖是一种能紧密结合眼镜蛇毒磷脂酶A2的树脂。基于CVF诱导旁观者红细胞溶解的能力,设计了一种快速简单的溶血试验,用于CVF的定性和定量测定。从眼镜蛇指名亚种的毒液中分离出CVF,并描述了其一些生化特性和理化参数。