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基于 DNA-Ag 纳米簇的无标记荧光分子信标用于构建多功能生物传感器。

A label-free fluorescent molecular beacon based on DNA-Ag nanoclusters for the construction of versatile Biosensors.

机构信息

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China; University of Chinese Academy of Sciences, Beijing 100039, China.

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China; University of Chinese Academy of Sciences, Beijing 100039, China; Department of Chemistry and Physics, State University of New York at Stony Brook, New York, NY 11794-3400, USA.

出版信息

Biosens Bioelectron. 2015 Dec 15;74:318-21. doi: 10.1016/j.bios.2015.06.044. Epub 2015 Jun 22.

Abstract

In this paper, we developed a simple, low-cost and sensitive DNA sequences detection biosensor based on a label-free molecular beacon (MB) whose DNA hairpin structure terminal has a guanine-rich sequence that can enhance fluorescence of silver nanoclusters (Ag NCs). Without hybridization between hairpin probe and target DNA, the Ag NCs presented bright fluorescence for the proximity of guanine-rich sequences (GRSs). After binding with target DNA, the hairpin shape was destroyed which results in a decrease of the Ag NCs fluorescence intensity. With this biosensor, we detected three disease-related genes that were the human immunodeficiency virus (HIV) gene, hepatitis B virus (HBV) gene and human T-lymphotropic virus type I (HTLV-I) gene. The detection limits based on S/N of 3 were 4.4 nM, 6.8 nM and 8.5 nM for HIV gene, HBV gene and HTLV-I gene, respectively. Our sensor was also of high selectivity and could distinguish even one nucleotide mismatched target.

摘要

在本文中,我们开发了一种简单、低成本且灵敏的 DNA 序列检测生物传感器,该传感器基于无标记的分子信标(MB),其 DNA 发夹结构末端具有富含鸟嘌呤的序列,可增强银纳米簇(Ag NCs)的荧光。在发夹探针与目标 DNA 之间没有杂交的情况下,Ag NCs 由于靠近富含鸟嘌呤的序列(GRSs)而呈现明亮的荧光。与目标 DNA 结合后,发夹形状被破坏,导致 Ag NCs 荧光强度降低。利用该生物传感器,我们检测了三种与疾病相关的基因,即人类免疫缺陷病毒(HIV)基因、乙型肝炎病毒(HBV)基因和人类 T 淋巴细胞白血病病毒 I 型(HTLV-I)基因。基于信噪比为 3 的检测限分别为 HIV 基因、HBV 基因和 HTLV-I 基因的 4.4 nM、6.8 nM 和 8.5 nM。我们的传感器还具有很高的选择性,即使是一个核苷酸错配的靶标也能区分。

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