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通过使用DNA修饰的氧化石墨烯传感器的滚环扩增对人唾液中的微小RNA进行超灵敏检测。

Ultrasensitive Detection of MicroRNA in Human Saliva via Rolling Circle Amplification Using a DNA-Decorated Graphene Oxide Sensor.

作者信息

Pitikultham Piyawat, Putnin Thitirat, Pimalai Dechnarong, Sathirapongsasuti Nuankanya, Kitiyakara Chagriya, Jiang Qiao, Ding Baoquan, Japrung Deanpen

机构信息

CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing 100190, China.

School of Nanoscience and Technology, University of Chinese Academy of Sciences, Beijing 100049, China.

出版信息

ACS Omega. 2023 Apr 17;8(17):15266-15275. doi: 10.1021/acsomega.3c00411. eCollection 2023 May 2.

Abstract

MicroRNAs (miRNAs) are a family of conserved small noncoding RNAs whose expression is associated with many diseases, including cancer. Salivary miRNAs are gaining popularity as noninvasive diagnostic biomarkers for cancer and other systemic disorders, but their use is limited by their low abundance and complicated detection procedure. Herein, we present a novel self-assembly approach based on rolling circle amplification (RCA) and graphene oxide (GO) for the ultrasensitive detection of miRNA21 and miRNA16 (miRNA oral cancer biomarkers in human saliva). First, target miRNA hybridizes with the RCA template. In the presence of DNA polymerase, the RCA reaction is induced and sequences matching the template are generated. Then, a nicking enzyme cuts the long ssDNA product into tiny pieces to obtain the amplified products. The DNA-decorated GO sensor was fabricated by preabsorbing the ssDNA fluorescence-labeled probe on the GO surface, resulting in fluorescence quenching. The DNA-decorated GO sensor could detect the amplified product via the self-assembly of dsDNA, leading to the desorption and recovery of the fluorescence-labeled probe. Under optimal conditions, the proposed system exhibited ultrasensitive detection; the detection limits of miRNA16 and miRNA21 were 8.81 and 3.85 fM, respectively. It showed a wide range of detection between 10 fM and 100 pM for miRNA16 and between 10 fM and 1 nM for miRNA16. It demonstrated high selectivity, distinguishing between 1- and 3-mismatch nucleotides in target miRNA. Overall, our proposed DNA-decorated GO sensor can accurately detect the salivary miRNAs and may potentially be used for the diagnosis and screening of early-stage oral cancer.

摘要

微小RNA(miRNA)是一类保守的小非编码RNA,其表达与包括癌症在内的多种疾病相关。唾液miRNA作为癌症和其他全身性疾病的非侵入性诊断生物标志物正越来越受到关注,但其应用受到低丰度和复杂检测程序的限制。在此,我们提出了一种基于滚环扩增(RCA)和氧化石墨烯(GO)的新型自组装方法,用于超灵敏检测miRNA21和miRNA16(人类唾液中的口腔癌生物标志物)。首先,靶miRNA与RCA模板杂交。在DNA聚合酶存在下,诱导RCA反应并生成与模板匹配的序列。然后,切口酶将长链单链DNA产物切割成小片段以获得扩增产物。通过将荧光标记的单链DNA探针预吸附在GO表面制备DNA修饰的GO传感器,导致荧光猝灭。DNA修饰的GO传感器可以通过双链DNA的自组装检测扩增产物,从而导致荧光标记探针的解吸和恢复。在最佳条件下,所提出的系统表现出超灵敏检测;miRNA16和miRNA21的检测限分别为8.81和3.85 fM。它对miRNA16的检测范围为10 fM至100 pM,对miRNA16的检测范围为10 fM至1 nM。它表现出高选择性,能够区分靶miRNA中与1个和3个错配的核苷酸。总体而言,我们提出的DNA修饰的GO传感器可以准确检测唾液中的miRNA,并可能潜在地用于早期口腔癌的诊断和筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d7f/10157686/0cf0dbf604e8/ao3c00411_0007.jpg

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