适体
化学
G-四倍体
动力学
生物物理学
离解(化学)
离解率
蛋白质二级结构
受体-配体动力学
分析物
纳米技术
鸟嘌呤
分子识别
组合化学
调制(音乐)
核糖开关
生物传感器
分子动力学
费斯特共振能量转移
作者
Connor D. Flynn,Dingran Chang,Yebin Lee,Scott E. Isaacson,Zhenwei Wu,Jonathan Rivnay,Shana O. Kelley
摘要
Aptamers have emerged as key receptors in the pursuit of universal biomolecular monitoring. However, while many aptamers possess excellent association rates, they tend to exhibit slow dissociation kinetics. While these slow off-rates are great for single-use applications, they pose a significant challenge for applications requiring continuous, repeated measurements where hysteresis complicates subsequent binding events. The G-quadruplex represents a common motif in many high-specificity aptamers and is composed of complexed guanine residues. Here, we present a method for modulating G-quadruplex aptamer binding kinetics through use of a polycytosine strand that can destabilize quadruplex structure and accelerate target release in a predictable manner. We demonstrate this phenomenon for several aptamer targets, including thrombin, interferon-gamma, and nucleolin, and highlight the ability of these modified aptamers to capture dynamic changes in analyte concentration on minute time scales.
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