Wallimann T, Zurbriggen B, Eppenberger H M
Enzyme. 1985;33(4):226-31. doi: 10.1159/000469437.
The mitochondrial isoenzyme of creatine kinase (MiMi-CK) was separated by affinity chromatography on Cibachrome-Blue-Sepharose (Sepharose-Blue, Pharmacia). While the soluble CK isoforms (BB-CK and MM-CK) were specifically eluted by raising the pH of the column buffer from pH 6.0 to pH 8.0, MiMi-CK remained bound under these conditions but was specifically eluted by subsequent addition of ADP to the pH 8.0 buffer. This one-step method allows a fast and efficient separation of MiMi-CK from MM-and BB-CK isoenzymes and at the same time an enrichment of MiMi-CK by about 50-fold. Since MiMi-CK can be assayed separately after isolation by affinity chromatography on Sepharose-Blue, this method may be of clinical importance.
通过在西巴铬蓝琼脂糖凝胶(琼脂糖蓝,Pharmacia公司)上进行亲和层析,分离出肌酸激酶的线粒体同工酶(MiMi-CK)。当通过将柱缓冲液的pH从6.0提高到8.0来特异性洗脱可溶性CK同工型(BB-CK和MM-CK)时,MiMi-CK在这些条件下仍保持结合状态,但随后向pH 8.0的缓冲液中添加ADP可将其特异性洗脱。这种一步法可快速有效地从MM-CK和BB-CK同工酶中分离出MiMi-CK,同时使MiMi-CK富集约50倍。由于通过在琼脂糖蓝上进行亲和层析分离后可单独测定MiMi-CK,因此该方法可能具有临床重要性。