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接力式 RNA/条码金纳米花杂交物用于总患者血清中 microRNA 的广泛和灵敏检测。

Relay-race RNA/barcode gold nanoflower hybrid for wide and sensitive detection of microRNA in total patient serum.

机构信息

School of Integrative Engineering, Chung-Ang University, Heukseok-dong, Dongjak-gu, Seoul, 06910, Republic of Korea.

Human IT Convergence Research Center, Convergence System R&D Division, Saenari-ro, Bundang-gu, Seongnam-si, Gyeonggi-do, 13509, Republic of Korea.

出版信息

Biosens Bioelectron. 2019 Sep 15;141:111468. doi: 10.1016/j.bios.2019.111468. Epub 2019 Jun 22.

Abstract

Development of a very sensitive biosensor is accompanied with an inevitable shrinkage in the linear detection range. Here, we developed an electrochemical biosensor with a novel methodology to detect microRNA-21 (miR21) at an ultralow level and broad linear detection range. A three-way junction RNA structure was designed harboring (i) a methylene blue (MB)-modified hairpin structure at its one leg to function as the sensing moiety and (ii) the other two legs to be further hybridized with barcode gold nanoparticles (MB/barG) as the signal amplifiers. Addition of target miR21 resulted in opening the hairpin moiety and subsequent hybridization with DNA-modified gold nanoflower/platinum electrode (GNF@Pt) to form the MB-3 sensor. Inspired by the relay-race run, to extend the dynamic detection range and increase the sensitivity of the biosensor, MB/barG was added to form the second detection modality (MBG-3). The combined sensor required very low sample volume (4 μL) and could identify 135 aM or 324 molecules of miR21 with the ability to operate within a wide linear range from 1 μM down to 500 aM. The fabricated GNF@Pt showed a remarkable conductivity compared with the gold nanoparticle-modified electrode. Addition of MB/barG boosted the electrochemical signal of the MB by almost 230 times. Moreover, a new protocol was introduced by the authors to increase the efficiency of microRNA extraction from the total serum. Possessing a sound selectivity and specificity towards single base-pair mutations, the developed biosensor could profile cancer development stages of two patient serums.

摘要

一种非常灵敏的生物传感器的开发伴随着线性检测范围不可避免的缩小。在这里,我们开发了一种电化学生物传感器,采用了一种新的方法来检测超低水平和宽线性检测范围的 microRNA-21(miR21)。设计了一种三链结 RNA 结构,其中(i)一个在其一条腿上修饰有亚甲蓝(MB)的发夹结构用作传感部分,(ii)另外两条腿进一步与条码金纳米粒子(MB/barG)杂交作为信号放大器。添加靶标 miR21 导致发夹部分打开,随后与 DNA 修饰的金纳米花/铂电极(GNF@Pt)杂交形成 MB-3 传感器。受接力赛跑的启发,为了扩展动态检测范围并提高生物传感器的灵敏度,添加了 MB/barG 以形成第二种检测模式(MBG-3)。该组合传感器需要非常小的样品量(4μL),能够识别 135 aM 或 324 个 miR21 分子,其线性范围从 1μM 扩展到 500 aM。与金纳米粒子修饰的电极相比,制备的 GNF@Pt 表现出显著的导电性。添加 MB/barG 使 MB 的电化学信号增强了近 230 倍。此外,作者引入了一种新的方案来提高从总血清中提取 microRNA 的效率。开发的生物传感器对单碱基对突变具有良好的选择性和特异性,能够对两个患者血清的癌症发展阶段进行分析。

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