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基于近邻杂交诱导的粒子 DNA walker 用于超灵敏蛋白质检测。

Proximity hybridization-induced on particle DNA walker for ultrasensitive protein detection.

机构信息

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, PR China.

State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, PR China.

出版信息

Anal Chim Acta. 2019 Oct 3;1074:142-149. doi: 10.1016/j.aca.2019.05.013. Epub 2019 May 8.

Abstract

A simple proximity hybridization-induced on particle DNA walker was designed for ultrasensitive detection of proteins, for example platelet-derived growth factor (PDGF-BB) secreted by cancer cells, in which the DNA walker was activated by specific target binding and powered by an enzymatic cleavage to produce amplified signal. High-density FAM-labeled hairpin oligonucleotides (FAM-DNA1) were functionalized on AuNPs to construct three-dimensional (3D) DNA tracks. The specific binding of PDGF-BB with two aptamer probes (DNA3 and DNA4) led to the proximity hybridization-induced DNA displacement and the free of DNA walker (DNA2) to perform movement on the 3D tracks by an enzymatic cleavage, resulting in the release of massive FAM-DNA1 fragments from the AuNPs and the generation of fluorescent signal. This DNA walker based sensing strategy could detect PDGF-BB in a concentration range of 4 orders of magnitude with a detection limit down to sub-pM level. The practical applicability of the assay was demonstrated by detecting PDGF-BB secreted from MCF-7 cells with satisfactory results. The proposed DNA walker based assay could conveniently detect PDGF-BB with high sensitivity and good accuracy, along with the good extensibility of the assay, showing promise for practical diagnosis.

摘要

设计了一种简单的基于粒子的邻近杂交诱导 DNA 分子梭,用于超灵敏检测蛋白质,例如癌细胞分泌的血小板衍生生长因子 (PDGF-BB),其中 DNA 分子梭通过特定靶标结合被激活,并通过酶切产生放大信号。高密度 FAM 标记的发夹寡核苷酸(FAM-DNA1)功能化在 AuNPs 上,以构建三维 (3D) DNA 轨道。PDGF-BB 与两个适体探针(DNA3 和 DNA4)的特异性结合导致邻近杂交诱导的 DNA 位移和 DNA 分子梭(DNA2)的释放,使其能够在 3D 轨道上通过酶切进行运动,从而导致大量 FAM-DNA1 片段从 AuNPs 上释放,并产生荧光信号。这种基于 DNA 分子梭的传感策略可以在 4 个数量级的浓度范围内检测 PDGF-BB,检测限低至亚皮摩尔水平。该测定法通过检测 MCF-7 细胞分泌的 PDGF-BB 证明了其实用性,结果令人满意。该基于 DNA 分子梭的测定法具有高灵敏度和良好准确性的特点,同时具有良好的可扩展性,有望用于实际诊断。

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