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用于直接从生物样品中灵敏检测微小RNA的微流控指数滚环扩增技术

Microfluidic Exponential Rolling Circle Amplification for Sensitive microRNA Detection Directly from Biological Samples.

作者信息

Cao Hongmei, Zhou Xin, Zeng Yong

机构信息

Department of Chemistry, University of Kansas, Lawrence, KS 66045.

University of Kansas Cancer Center, Kansas City, KS 66160.

出版信息

Sens Actuators B Chem. 2019 Jan 15;279:447-457. doi: 10.1016/j.snb.2018.09.121. Epub 2018 Oct 4.

Abstract

There is an urgent need of sensitive bioanalytical platforms for sensitive and precise quantification of low-abundance microRNA targets in complex biological samples, including liquid biopsies of tumors. Many of current miRNA biosensing methods require laborious sample pretreatment procedures, including extraction of total RNA, which largely limits their biomedical and clinical applications. Herein we developed an integrated Microfluidic Exponential Rolling Circle Amplification (MERCA) platform for sensitive and specific detection of microRNAs directly in minimally processed samples. The MERCA system integrates and streamlines solid-phase miRNA isolation, miRNA-adapter ligation, and a dualphase exponential rolling circle amplification (eRCA) assay in one analytical workflow. By marrying the advantages of microfluidics in leveraging bioassay performance with the high sensitivity of eRCA, our method affords a remarkably low limit of detection at <10 zeptomole levels, with the ability to discriminate single-nucleotide difference. Using the MERCA chip, we demonstrated quantitative detection of miRNAs in total RNA, raw cell lysate, and cellderived exosomes. Comparing with the parallel TaqMan RT-qPCR measurements verified the adaptability of the MERCA system for detection of miRNA biomarkers in complex biological materials. In particular, high sensitivity of our method enables direct detection of low-level exosomal miRNAs in as few as 2 × 10 exosomes. Such analytical capability immediately addresses the unmet challenge in sample consumption, a key setback in clinical development of exosome-based liquid biopsies. Therefore, the MERCA would provide a useful platform to facilitate miRNA analysis in broad biological and clinical applications.

摘要

迫切需要灵敏的生物分析平台,用于对复杂生物样品(包括肿瘤液体活检样品)中的低丰度微小RNA靶标进行灵敏且精确的定量分析。当前许多微小RNA生物传感方法需要繁琐的样品预处理程序,包括总RNA提取,这在很大程度上限制了它们在生物医学和临床中的应用。在此,我们开发了一种集成的微流控指数滚环扩增(MERCA)平台,用于直接在经过最少处理的样品中灵敏且特异性地检测微小RNA。MERCA系统在一个分析流程中集成并简化了固相微小RNA分离、微小RNA-衔接子连接以及双相指数滚环扩增(eRCA)分析。通过将微流控在提升生物分析性能方面的优势与eRCA的高灵敏度相结合,我们的方法实现了低至<10 zeptomole水平的极低检测限,并且能够区分单核苷酸差异。使用MERCA芯片,我们展示了在总RNA、原始细胞裂解液和细胞衍生外泌体中对微小RNA的定量检测。与平行的TaqMan RT-qPCR测量结果相比较,验证了MERCA系统在复杂生物材料中检测微小RNA生物标志物的适用性。特别是,我们方法的高灵敏度能够直接在仅2×10个外泌体中检测低水平的外泌体微小RNA。这种分析能力立即解决了样品消耗方面尚未满足的挑战,这是基于外泌体的液体活检临床开发中的一个关键障碍。因此,MERCA将为在广泛的生物学和临床应用中促进微小RNA分析提供一个有用的平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35fe/6284813/42cfd54a08f9/nihms-1509838-f0001.jpg

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