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使用连接到铽配合物的发光适体传感器直接检测未稀释血清中的腺苷。

Direct detection of adenosine in undiluted serum using a luminescent aptamer sensor attached to a terbium complex.

机构信息

Department of Chemistry, University of Illinois at Urbana-Champaign, 61801, United States.

出版信息

Anal Chem. 2012 Sep 18;84(18):7852-6. doi: 10.1021/ac302167d. Epub 2012 Aug 28.

Abstract

Aptamers, single-stranded nucleic acids that can selectively bind to various target molecules, have been widely used for constructing biosensors. A major challenge in this field, however, is direct sensing of analytes in complex biological media such as undiluted serum. While progress has been made in developing an inhomogeneous assay by using a preseparation step to wash away the interferences within serum, a facile strategy for direct detection of targets in homogeneous unprocessed serum is highly desired. We herein report a turn-on luminescent aptamer biosensor for the direct detection of adenosine in undiluted and unprocessed serum, by taking advantage of a terbium chelate complex with long luminescence lifetime to achieve time-resolved detection. The sensor exhibits a detection limit of 60 μM adenosine while marinating excellent selectivity that is comparable to those in buffer. The approach demonstrated here can be applied for direct detection and quantification of a broad range of analytes in biological media by using other aptamers.

摘要

适体是一种单链核酸,能够选择性地结合各种靶分子,已被广泛用于构建生物传感器。然而,该领域的一个主要挑战是直接检测复杂生物介质(如未稀释的血清)中的分析物。虽然通过使用预分离步骤来清除血清中的干扰物,已经在开发非均相测定方面取得了进展,但仍需要一种简便的策略来直接检测均相未处理血清中的靶标。本研究报告了一种基于镧系元素螯合物复合物的上转换发光适体生物传感器,用于直接检测未稀释和未处理血清中的腺苷,利用其长荧光寿命实现了时间分辨检测。该传感器对腺苷的检测限为 60 μM,同时保持了与缓冲液相当的优异选择性。本研究中展示的方法可以通过使用其他适体,直接检测和定量生物介质中的广泛分析物。

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