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适体包被的纳米晶体量子点:一种无标记蛋白质检测的新方法。

Aptamer-capped nanocrystal quantum dots: a new method for label-free protein detection.

作者信息

Choi Jong Hyun, Chen Kok Hao, Strano Michael S

机构信息

Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.

出版信息

J Am Chem Soc. 2006 Dec 13;128(49):15584-5. doi: 10.1021/ja066506k.

Abstract

We demonstrate that aptamer-capped near-infrared PbS quantum dots (QDs) can detect a target protein based on selective charge transfer. The water-soluble QDs are synthesized with the thrombin-binding aptamer, which retains the secondary quadruplex structure necessary for binding to thrombin. These QDs have diameters of 3-6 nm and fluoresce around 1050 nm. When the aptamer-functionalized QD binds to its target, a fluorescence quenching occurs due to charge transfer from amine groups on the protein to the QD. Thrombin is detected within 1 min with a detection limit of approximately 1 nM. This selective detection is observed even in the presence of high background concentrations of interfering negatively or positively charged proteins, suggesting that aptamer-capped QDs could be useful for label-free protein assays.

摘要

我们证明,适配体封端的近红外硫化铅量子点(QDs)能够基于选择性电荷转移来检测目标蛋白质。水溶性量子点是与凝血酶结合适配体一起合成的,该适配体保留了与凝血酶结合所需的二级四重结构。这些量子点的直径为3 - 6纳米,在1050纳米左右发出荧光。当适配体功能化的量子点与其靶标结合时,由于蛋白质上的胺基团向量子点的电荷转移,会发生荧光猝灭。在1分钟内即可检测到凝血酶,检测限约为1纳摩尔。即使在存在高背景浓度的带负电荷或正电荷的干扰蛋白质的情况下,也能观察到这种选择性检测,这表明适配体封端的量子点可用于无标记蛋白质检测。

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