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基于荧光偏振的置换分析法用于测定与适配体结合的小分子。

Fluorescence polarization based displacement assay for the determination of small molecules with aptamers.

作者信息

Cruz-Aguado Jorge A, Penner Gregory

机构信息

NeoVentures Biotechnology Inc., 700 Collip Circle, London, Ontario, N6G 4X8, Canada.

出版信息

Anal Chem. 2008 Nov 15;80(22):8853-5. doi: 10.1021/ac8017058. Epub 2008 Oct 24.

Abstract

The conversion of an aptamer-target binding event into a detectable signal is an important step in the development of aptamer-based sensors. In this work, we show that the displacement of a fluorescently labeled oligo from the aptamer by the target can be detected by fluorescence polarization (FP). We used Ochratoxin A (OTA), a small organic molecule (MW = 403) as a case study. A detection limit of 5 nM OTA was achieved. The method presented here provides an advantage over fluorophore-quenching systems and other steady-state fluorescence approaches in that no modification of the aptamer or the target is required. Additionally, the signal is produced by the displacement event itself, so no further aggregation or conformational events have to be considered. This analytical method is particularly useful for small targets, as for large targets a direct measurement of the FP change of a labeled aptamer upon binding can be used to determine the concentration of the target. The results presented here demonstrate that aptamers and inexpensive labeled oligos can be used for rapid, sensitive, and specific determination of small molecules by means of FP.

摘要

将适体与靶标的结合事件转化为可检测信号是基于适体的传感器开发中的重要一步。在本研究中,我们表明通过荧光偏振(FP)可以检测到靶标将荧光标记的寡核苷酸从适体上置换下来。我们以赭曲霉毒素A(OTA)这种小分子有机化合物(分子量=403)为例进行了研究。实现了对OTA 5 nM的检测限。本文提出的方法相对于荧光团猝灭系统和其他稳态荧光方法具有优势,因为无需对适体或靶标进行修饰。此外,信号由置换事件本身产生,因此无需考虑进一步的聚集或构象变化。这种分析方法对于小分子靶标特别有用,因为对于大分子靶标,可以直接测量结合后标记适体的FP变化来确定靶标的浓度。此处给出的结果表明,适体和廉价的标记寡核苷酸可用于通过FP快速、灵敏且特异性地测定小分子。

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