计算生物学
亚型
DNA
生物
仿形(计算机编程)
计算机科学
模块化(生物学)
表型
纳米技术
DNA测序
蛋白质组学
分子生物物理学
基因组学
破译
化学
环介导等温扩增
作者
Meirong Cui,Chenxu Hu,Jiahan Dong,Yiyu Cheng,Bicheng Sun,Chunhai Fan,Lianhui Wang,Jie Chao
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-02-12
卷期号:20 (7): 5904-5917
被引量:1
标识
DOI:10.1021/acsnano.5c18968
摘要
Molecular classification of diseases that accurately reflects clinical behavior is fundamental to the realization of precision medicine. Single-cell protein analysis combined with coding technology offers a promising approach for constructing robust molecular classifiers. However, the low abundance of disease-related cells and the technical challenges in parallel profiling of multiple proteins remain major obstacles. Herein, we present a DNA nanostructure-based multicomponent coding strategy that enables multiprotein analysis at the single-cell level by precisely controlling the stoichiometry, orientation, and modularity of the magnetized tags and multicolor fluorescent tags. Compared with conventional linear DNA barcoding methods, our approach allows for the simultaneous magnetic separation of heterogeneous cell populations and multicolor fluorescence-based phenotypic encoding. By integrating single-cell trapping techniques, we demonstrate the accurate molecular subtyping of breast cancer based on fluorescence-encoded phenotypic features. This strategy expands the scope of applications in cell sorting, proteomic profiling, and genomic analysis, thus advancing the frontiers of precision medicine.
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