McKay E J
Immunol Lett. 1981 Nov;3(5):303-8. doi: 10.1016/0165-2478(81)90010-9.
Plasma C1q from human, rat, rabbit, dog and sheep were isolated by a 2-step affinity chromatography procedure. In the first step the method exploits the affinity of C1q for heparin and in the second the interaction between C1q and IgG. The precipitation of C1q by the SO4(2-) groups in agarose gels was used as a means to rapidly monitor the elution of C1q. This interaction was found to be non-species specific and therefore obviates the need for immunochemical and/or haemolytic assays. The isolation procedure is rapid, simple and is not confined to one species. Pure functionally active C1q was obtained from all species in yields of approximately 85-95%.
通过两步亲和层析法从人、大鼠、兔、狗和绵羊中分离出血浆C1q。第一步利用C1q对肝素的亲和力,第二步利用C1q与IgG之间的相互作用。利用琼脂糖凝胶中SO4(2-)基团对C1q的沉淀作用作为快速监测C1q洗脱的手段。发现这种相互作用是非物种特异性的,因此无需免疫化学和/或溶血试验。该分离方法快速、简单,不限于单一物种。从所有物种中均获得了纯度高且具有功能活性的C1q,产率约为85%-95%。