Isolation of Late Complement Components by Affinity Chromatography. II. Purification of the Human Complement Component C6

E.W. Rauterberg , G. Hänsch, U. Rother
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引用次数: 5

Abstract

We developed a new procedure for the rapid and gentle isolation of the human complement component C6 comparable to that described previously for C9. The procedure is based on affinity chromatography. As a first step, C6 is immunoabsorbed on insolubilized anti-C6 antibodies. These antibodies were derived from C6-defective rabbits (Freiburg strain). C6 was eluted with 3 M thiocyanate, pH 7.2, with a recovery of 15-23% of its hemolytic activity and a more than 270-fold purification. Impurities were removed in a second step by an «anti impurity» column. The final product yielded a 12% recovery of the hemolytic activity and the purification factor was higher than 1300. The final product was homogeneous in SDS polyacrylamide and immunoelectrophoresis.

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亲和色谱法分离晚期补体成分。2人补体成分C6的纯化
我们开发了一种新的程序,用于快速和温和地分离人补体成分C6,与之前描述的C9相当。该程序是基于亲和色谱法。作为第一步,C6被不溶性抗C6抗体免疫吸收。这些抗体来源于c6缺陷兔(Freiburg株)。用3 M硫氰酸盐(pH 7.2)洗脱C6,其溶血活性回收率为15-23%,纯化率超过270倍。杂质在第二步通过“反杂质”柱去除。最终产物的溶血活性回收率为12%,纯化系数高于1300。最终产物在SDS聚丙烯酰胺和免疫电泳中均质。
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