Key Laboratory of Zoonosis, Ministry of Education, Institute of Zoonosis, College of Veterinary Medicine, Jilin University, Changchun 130062, PR China.
Key Laboratory of Zoonosis, Ministry of Education, Institute of Zoonosis, College of Veterinary Medicine, Jilin University, Changchun 130062, PR China.
Biosens Bioelectron. 2015 Apr 15;66:559-64. doi: 10.1016/j.bios.2014.12.025. Epub 2014 Dec 9.
In this work, a double-probe based immunoassay was developed for rapid and sensitive determination of β-casein in bovine milk samples. In the method, magnetic beads (MBs), employed as supports for the immobilization of anti-β-casein polyclonal antibody (PAb), were used as the capture probe. Colloidal gold nanoparticles (AuNPs), employed as a bridge for loading anti-β-casein monoclonal antibody (McAb) and horseradish peroxidase (HRP), were used as the amplification probe. The presence of β-casein causes the sandwich structures of MBs-PAb-β-casein-McAb-AuNPs through the interaction between β-casein and the anti-β-casein antibodies. The HRP, used as an enzymatic-amplified tracer, can catalytically oxidize the substrate 3,3',5,5'-tetramethylbenzidine (TMB), generating optical signals that are proportional to the quantity of β-casein. The linear range of the immunoassay was from 6.5 to 1520ngmL(-1). The limit of detection (LOD) was 4.8ngmL(-1) which was 700 times lower than that of MBs-antibody-HRP based immunoassay and 6-7 times lower than that from the microplate-antibody-HRP based assay. The recoveries of β-casein from bovine milk samples were from 95.0% to 104.3% that had a good correlation coefficient (R(2)=0.9956) with those obtained by an official standard Kjeldahl method. For higher sensitivity, simple sample pretreatment and shorter time requirement of the antigen-antibody reaction, the developed immunoassay demonstrated the viability for detection of β-casein in bovine milk samples.
在这项工作中,开发了一种基于双探针的免疫测定法,用于快速灵敏地测定牛奶奶样中的β-酪蛋白。在该方法中,磁性珠(MBs)用作固定抗β-酪蛋白多克隆抗体(PAb)的载体,用作捕获探针。胶体金纳米粒子(AuNPs)用作加载抗β-酪蛋白单克隆抗体(McAb)和辣根过氧化物酶(HRP)的桥梁,用作放大探针。β-酪蛋白的存在通过β-酪蛋白与抗β-酪蛋白抗体之间的相互作用引起 MBs-PAb-β-酪蛋白-McAb-AuNPs 的夹心结构。作为酶放大示踪剂的 HRP 可以催化底物 3,3',5,5'-四甲基联苯胺(TMB)的氧化,产生与β-酪蛋白量成正比的光学信号。免疫测定的线性范围为 6.5 至 1520ngmL(-1)。检测限(LOD)为 4.8ngmL(-1),比 MBs-抗体-HRP 免疫测定低 700 倍,比微孔板-抗体-HRP 测定低 6-7 倍。从牛奶奶样中回收的β-酪蛋白的回收率为 95.0%至 104.3%,与通过官方标准凯氏定氮法获得的回收率具有良好的相关性(R(2)=0.9956)。为了提高灵敏度、简化样品预处理和缩短抗原抗体反应时间,该免疫测定法显示出在牛奶奶样中检测β-酪蛋白的可行性。