Nucleic-Acid-binding chromophores as efficient indicators of aptamer-target interactions.

IF 1.3 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Nucleic Acids Pub Date : 2012-01-01 Epub Date: 2012-10-10 DOI:10.1155/2012/247280
Kwabena Sarpong, Bhaskar Datta
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引用次数: 15

Abstract

The binding affinity and specificity of nucleic acid aptamers have made them valuable candidates for use as sensors in diagnostic applications. In particular, chromophore-functionalized aptamers offer a relatively simple format for detection and quantification of target molecules. We describe the use of nucleic-acid-staining reagents as an effective tool for detecting and signaling aptamer-target interactions. Aptamers varying in size and structure and targeting a range of molecules have been used in conjunction with commercially available chromophores to indicate and quantify the presence of cognate targets with high sensitivity and selectivity. Our assay precludes the covalent modification of nucleic acids and relies on the differential fluorescence signal of chromophores when complexed with aptamers with or without their cognate target. We also evaluate factors that are critical for the stability of the complex between the aptamer and chromophore in presence or absence of target molecules. Our results indicate the possibility of controlling those factors to enhance the sensitivity of target detection by the aptamers used in such assays.

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核酸结合发色团作为适体-靶标相互作用的有效指标。
核酸适体的结合亲和力和特异性使它们成为诊断应用中传感器的有价值的候选者。特别是,发色团功能化适配体为检测和定量靶分子提供了相对简单的格式。我们描述了使用核酸染色试剂作为检测和信号适体-靶标相互作用的有效工具。不同大小和结构的适体和靶向一系列分子已与商业上可获得的发色团结合使用,以高灵敏度和选择性指示和量化同源目标的存在。我们的测定排除了核酸的共价修饰,并依赖于与具有或不具有同源靶标的适体络合时发色团的差异荧光信号。我们还评估了在靶分子存在或不存在的情况下适体和发色团之间复合物稳定性的关键因素。我们的研究结果表明,通过控制这些因素来提高适体检测靶的灵敏度是可能的。
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来源期刊
Journal of Nucleic Acids
Journal of Nucleic Acids BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
3.10
自引率
21.70%
发文量
5
审稿时长
12 weeks
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