核糖核酸
化学
多路复用
小RNA
质谱法
寡核苷酸
计算生物学
多路复用
生物物理学
纳米技术
生物
生物化学
生物信息学
基因
色谱法
计算机科学
材料科学
电信
作者
Zhenzhen Zhang,Hongmei Xu,Yinyin Fan,Xue Zhang,Wei Wang,Jun‐Jie Zhu,Qianhao Min
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-02-15
卷期号:23 (5): 1820-1829
被引量:11
标识
DOI:10.1021/acs.nanolett.2c04690
摘要
Multiplexed profiling of RNAs aids in a comprehensive understanding of multiparameter-defined cellular processes and pathological states. We herein present a mass nanotags-enabled interfacial assembly system (MNTs-AS) with parallel amplification motors for simultaneous assaying of multiple RNAs in biosystems by matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS). Four kinds of MNTs encoding corresponding RNA can be cyclically assembled on magnetic beads by target-triggered catalytic hairpin assembly (CHA) machineries on nanointerfaces, generating multiplexed and amplified characteristic ion signals assigned to target RNAs upon MALDI MS interrogation. By virtue of high sensitivity and multiplexing capability, the MNTs-AS-based MS assay allows precision subtyping of diverse breast cancer cells and their exosomes by multiplexed profiling of miRNA-21, miRNA-373, miRNA-155, and manganese superoxide dismutase mRNA via a single MS inquiry. This method provides a promising tool for unraveling multiple RNA-involved biological events in fundamental research and distinguishing different cancer subtypes in clinical practice.
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