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基于单链发夹结构的生物传感器模型,用于高灵敏度检测多种目标。

Biosensor model based on single hairpin structure for highly sensitive detection of multiple targets.

机构信息

College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022, P. R. China.

State Key Laboratory for Chemo/Biosensing and Chemometrics, Hunan University, Changsha 410082, P. R. China.

出版信息

Anal Methods. 2023 Aug 31;15(34):4220-4225. doi: 10.1039/d3ay01049j.

Abstract

Nowadays, due to the genetic information carried by nucleic acids, they can serve as a biomarker for the early diagnosis of diseases, including tumors and cardiovascular disease, among others, making genetic testing a hotspot of biomedicine. Therefore, we have designed a universal fluorescence biosensor that can detect multiple DNA sequences with good performance. In our designed biosensor, exonuclease is used due to its ability to digest double-stranded DNA from the phosphorylated 5'- end and promote the targeted cycle. The exonuclease is introduced into a DNA hairpin containing a target recognition sequence. Hence, with the target, exonuclease-assisted targeted recycling can be activated. The hydrolyzed DNA hairpin triggers a strand displacement reaction between the hairpin probe (H1) and F-Q double DNA strand (F-Q), increasing the distance between the fluorescent chain (F) and quenching chain (Q); thus the fluorescence signal is emitted. It is exciting that the detection limit of the biosensor is 300 fM, which is relatively low, and there is an excellent linear relationship between fluorescence intensity and target concentration. Moreover, the biosensor we designed has universal applicability in the detection of other genes, and the range of RSD is 1.28-2.45%. Hence, it has good application prospects and practical value in the early detection of some diseases and the design of fluorescent biosensors.

摘要

如今,由于核酸所携带的遗传信息,它们可以作为疾病(包括肿瘤和心血管疾病等)早期诊断的生物标志物,使基因检测成为生物医学的热点。因此,我们设计了一种通用的荧光生物传感器,能够以良好的性能检测多种 DNA 序列。在我们设计的生物传感器中,由于外切酶能够从磷酸化的 5' 端消化双链 DNA,并促进靶向循环,因此被用于检测。外切酶被引入到含有目标识别序列的 DNA 发夹中。因此,有了目标,外切酶辅助的靶向循环就可以被激活。被水解的 DNA 发夹引发发夹探针 (H1) 和 F-Q 双链 (F-Q) 之间的链置换反应,增加荧光链 (F) 和猝灭链 (Q) 之间的距离;从而发出荧光信号。令人兴奋的是,该生物传感器的检测限低至 300 fM,荧光强度与目标浓度之间存在极好的线性关系。此外,我们设计的生物传感器在检测其他基因方面具有通用性,其 RSD 范围为 1.28-2.45%。因此,它在某些疾病的早期检测和荧光生物传感器的设计方面具有良好的应用前景和实用价值。

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