Choi M J, Choe I S, Kang H K, Lee J S, Chung T W
Genetic Engineering Center, Korea Institute of Science and Technology, Seoul.
Clin Chem. 1991 May;37(5):673-7.
A multiple enzyme immunoassay (multi-EIA) was developed to quantify whole-molecule human choriogonadotropin (w-hCG) and free hCG beta-subunits (hCG-beta) simultaneously. A clone of a specific monoclonal antibody was coupled to solid phase; two other clones of different monoclonal antibodies were conjugated to horseradish peroxidase (HRP; EC 1.11.1.7) and alkaline phosphatase (AP; EC 3.1.3.1), respectively. These two enzyme conjugates were mixed together to measure w-hCG or hCG-beta, depending on the selection of the enzyme substrate. To measure w-hCG and hCG-beta simultaneously, both enzyme substrates were used with the blended enzyme conjugates. The assay is simple and reproducible, and can be completed within 2 h with high specificity and sensitivity. We measured w-hCG and hCG-beta in the sera of women with abnormal pregnancies and in patients with tumors of the reproductive system, and observed different hCG-beta/w-hCG ratios in patients with various types of trophoblastic tumors.
开发了一种多酶免疫测定法(multi-EIA)以同时定量全分子人绒毛膜促性腺激素(w-hCG)和游离hCGβ亚基(hCG-β)。将一种特异性单克隆抗体的克隆与固相偶联;另外两种不同单克隆抗体的克隆分别与辣根过氧化物酶(HRP;EC 1.11.1.7)和碱性磷酸酶(AP;EC 3.1.3.1)偶联。将这两种酶结合物混合在一起以根据酶底物的选择来测量w-hCG或hCG-β。为了同时测量w-hCG和hCG-β,两种酶底物与混合的酶结合物一起使用。该测定法简单且可重复,并且可以在2小时内完成,具有高特异性和灵敏度。我们测量了妊娠异常女性血清和生殖系统肿瘤患者血清中的w-hCG和hCG-β,并观察到不同类型滋养层细胞瘤患者的hCG-β/w-hCG比值不同。