适体
化学
等温滴定量热法
离解常数
砷
生物传感器
结合位点
结合常数
分子结合
DNA
结合亲和力
指数富集配体系统进化
纳米技术
组合化学
生物物理学
生物化学
分子
分子生物学
有机化学
核糖核酸
基因
受体
生物
材料科学
作者
Chenghua Zong,Juewen Liu
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2019-07-25
卷期号:91 (16): 10887-10893
被引量:93
标识
DOI:10.1021/acs.analchem.9b02789
摘要
An arsenic-binding aptamer named Ars-3 was reported in 2009, and it has been used for detection of As(III) in more than two dozen papers. In this work, we performed extensive binding assays using isothermal titration calorimetry, various DNA-staining dyes, and gold nanoparticles. By carefully comparing Ars-3 and a few random control DNA sequences, no specific binding of As(III) was observed in each case. Therefore, we conclude that Ars-3 cannot bind As(III). Possible reasons for some of the previously reported binding and detection were speculated to be related to the adsorption of As(III) onto gold surfaces, which were used in many related sensor designs, and As(III)/Au interactions were not considered before. The selection data in the original paper were then analyzed in terms of sequence alignment, secondary structure prediction, and dissociation constant measurement. These steps need rigorous testing before confirming specific binding of newly selected aptamers. This study calls for attention to the gap between aptamer selection and biosensor design, and the gap needs to be filled by careful binding assays to further the growth of the aptamer field.
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