Lee S H, Cho M H
Department of Biochemistry, College of Medicine, Soonchunhyang University, Cheon-An, Korea.
J Korean Med Sci. 1996 Oct;11(5):390-6. doi: 10.3346/jkms.1996.11.5.390.
We prepared two monoclonal antibodies-A-I30 and A-I4 to HDL apo A-I-with the ultimate goals of expressing and overproducing the valuable immunodiagnostic single chain Fv by phage display libraries in E, coli. Monoclonal antibodies were produced by immunizing mice with apolipoprotein A-I, and purified from ascitic fluid by affinity chromatography on a Protein A Sepharose CL-4B column. The specificity of A-I30 and A-I4 was confirmed by ELISA and Western blotting. The dissociation constants(Kd) of antigen-antibody complex obtained by enzyme linked immunosorbent assay(ELISA) method were 2.25 x 10(-8) M for A-I30 and 2.15 x 10(-8) M for A-I4. The experimental values of Kd are shown to be close to those obtained by immunoprecipitation of the radiolabeled antigen. From the above results, it was shown that A-I30 and A-I4 could be provided as excellent reagents for the determination of plasma HDL concentrations in clinical specimens using ELISA.
我们制备了两种针对高密度脂蛋白载脂蛋白A-I的单克隆抗体——A-I30和A-I4,最终目标是通过噬菌体展示文库在大肠杆菌中表达并过量生产有价值的免疫诊断单链Fv。用载脂蛋白A-I免疫小鼠产生单克隆抗体,并通过在蛋白A琼脂糖CL-4B柱上进行亲和层析从腹水液中纯化。通过酶联免疫吸附测定(ELISA)和蛋白质印迹法确认了A-I30和A-I4的特异性。通过酶联免疫吸附测定(ELISA)方法获得的抗原-抗体复合物的解离常数(Kd),A-I30为2.25×10(-8)M,A-I4为2.15×10(-8)M。Kd的实验值显示与通过放射性标记抗原免疫沉淀获得的值接近。从上述结果表明,A-I30和A-I4可作为使用ELISA测定临床标本中血浆高密度脂蛋白浓度的优良试剂。