辣根过氧化物酶
单克隆抗体
化学
蛋白质A
胶体金
基质(水族馆)
抗原
靶蛋白
纳米颗粒
分子生物学
蛋白质G
免疫分析
抗体
蛋白质检测
酶
纳米技术
材料科学
生物化学
生物
基因
免疫学
生态学
遗传学
作者
Chun Ping Jia,Xiao Qin Zhong,Hua Bao,Mei Ying Liu,Feng Jing,Xin Hui Lou,Shuochao Yao,Jia Xiang,Qing Jin,Jian Zhao
标识
DOI:10.1016/j.bios.2009.02.024
摘要
Highly sensitive protein detection method based on nanoparticles and enzyme-linked immunosorbent assays (ELISAs), named Nano-ELISA, was introduced. In this method, the micro-magnetic beads were modified with monoclonal antibody of the target protein p53. Gold nanoparticles (AuNPs) were modified with another monoclonal detector antibody and Horseradish peroxidase (HRP, for signal amplification). The presence of target protein p53 causes the formation of the sandwich structures (magnetic beads–target protein–AuNP probes) through the interaction between the antibodies and the antigen p53. The HRP at the surface of AuNPs catalytically oxidize the substrate and generate optical signals that reflected the quantity of the target protein. Down to 5 pg mL−1 of protein was detected in less than 2 h with this method. The detection sensitivity of p53 classic ELISA kit is 0.125 ng mL−1. This method is as simple as ELISA and has higher sensitivity than ELISA, which can potentially be exploited in clinic. This method can be used to detect protein markers of tumors, nervous system or other diseases for early diagnostics.
科研通智能强力驱动
Strongly Powered by AbleSci AI