适体
结合
肽
荧光
检出限
化学
组合化学
滚动圆复制
镉
生物传感器
色谱法
生物物理学
生物化学
生物
分子生物学
DNA
有机化学
量子力学
数学分析
物理
DNA复制
数学
作者
Kaimin Peng,Jiahao Sha,Xian-wen Fang,Mengqiu Li,Jingsong Yu,Li Wang,Fei Xu
标识
DOI:10.1021/acs.jafc.3c08636
摘要
The existing aptamers for cadmium (Cd2+), the common toxic heavy metal contaminant in food, cannot meet the requirements for detecting Cd2+ in rapid detection methods. In previous work, we found that coupling aptamer–peptide conjugates (APCs) with peptides and aptamers can provide a less disruptive method with a significantly improved affinity. Moreover, we found that the spatial conformation of aptamers and peptides is crucial for obtaining proper affinity in APC. Therefore, we describe a simple design strategy to obtain a series of APCs with different affinities by designing peptide orientations (N-terminal, C-terminal). The best affinity was found for APC(C1–N) with a binding constant (Ka) of 2.23 × 106 M–1, indicating that the APC(C1–N) affinity was significantly increased by 829.17% over aptamer. Finally, a rolling-circle amplification (RCA)-coupled ratio fluorescence-based biosensor for Cd2+ detection was established with a detection limit of 0.0036 nM, which has great potential for practical aquatic product detection.
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