Urdal P, Kierulf P
Clin Chem. 1981 Jan;27(1):83-7.
We have developed an equilibrium radioimmunoassay for creatine kinase BB (CK-BB) isoenzyme in serum. We used as antibody a CK-BB binding immunoglobulin G isolated from serum of a patient with macro CK-BB. Free and antibody-bound tracer were separated by anion-exchange chromatography. The affinity constant, Keq, for the binding of CK-BB to immunoglobulin was calculated as 1.4 X 10(11) L/mol, which suggests that the immunoglobulin was an autoantibody. The assay may detect 1 microgram of enzyme per liter in a 100- microL sample. CK-MM and CK-MB isoenzymes did not cross react in the assay. Within-assay precision (CV) was 5%; between-assay precision was 14 and 15% at 6 and 14 microgram of CK-BB per liter, respectively. Of 45 sera from blood donors, 95% contained < 1.8 microgram of CK-BB per liter, whereas of 19 sera from unselected patients the corresponding figure was 2.8 microgram/L.
我们已开发出一种用于检测血清中肌酸激酶BB(CK - BB)同工酶的平衡放射免疫分析法。我们使用从一名患有巨CK - BB的患者血清中分离出的与CK - BB结合的免疫球蛋白G作为抗体。游离的和与抗体结合的示踪剂通过阴离子交换色谱法分离。计算得出CK - BB与免疫球蛋白结合的亲和常数Keq为1.4×10¹¹L/mol,这表明该免疫球蛋白是一种自身抗体。该分析法在100微升样品中可检测到每升1微克的酶。CK - MM和CK - MB同工酶在该分析法中不发生交叉反应。批内精密度(CV)为5%;在每升含有6微克和14微克CK - BB时,批间精密度分别为14%和15%。在45份献血者的血清中,95%的血清每升含有的CK - BB小于1.8微克,而在19份未经过挑选的患者血清中,相应数字为2.8微克/升。