Aptamers as Versatile Molecular Tools for Antibody Production Monitoring and Quality Control

化学 适体 指数富集配体系统进化 抗体 分子信标 曲妥珠单抗 计算生物学 寡核苷酸 DNA 生物化学 分子生物学 免疫学 癌症 生物 基因 乳腺癌 遗传学 核糖核酸
作者
Kaiming Chen,Jie Zhou,Zhentao Shao,Jia Liu,Jia Song,Ruowen Wang,Juan Li,Weihong Tan
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:142 (28): 12079-12086 被引量:64
标识
DOI:10.1021/jacs.9b13370
摘要

Antibody drugs have been used to treat many diseases, and to date, this has been the most rapidly growing drug class. However, the lack of suitable methods for real-time and high-throughput monitoring of antibody production and quality control has been a hindrance to the further advancement of antibody drugs or biosimilars. Therefore, we herein report a versatile tool for one-step fluorescence monitoring of antibody production by using aptamer probes selected through the in vitro SELEX method. In this case, DNA aptamers were selected against the humanized IgG1 antibody drug trastuzumab with high specificity and affinity with a Kd value of aptamer CH1S-3 of 10.3 nM. More importantly, the obtained aptamers were able to distinguish native from heat-treated, whereas antibodies failed this test. On the basis of the advantages of rapid detection for aptamers, we designed aptamer molecular beacons for direct and sensitive detection of trastuzumab in complex samples. Unlike traditional antibody-based ELISA, the signal was observed directly upon interaction with the target without the need for time-consuming binding and multiple washing steps. To further highlight biomedical applications, the use of aptamers as potential tools for quality control and traceless purification of antibody drugs was also demonstrated. Thus, aptamers are shown to be promising alternatives for antibody production monitoring, quality control, and purification, providing technical support to accelerate antibody drug development.
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