微流控
细胞外小泡
化学
小泡
癌症生物标志物
细胞外
纳米技术
生物标志物发现
生物物理学
蛋白质组学
癌症
材料科学
生物化学
细胞生物学
生物
膜
基因
遗传学
作者
Qi Niu,Yun Shu,Yuanqiang Chen,Zhi Huang,Zhixian Yao,Xiaofeng Chen,Fanghe Lin,Jianzhou Feng,Chen Huang,Hua Wang,Hong‐ming Ding,Chaoyong Yang,Lingling Wu
标识
DOI:10.1002/anie.202215337
摘要
Isolation and analysis of tumor-derived extracellular vesicles (T-EVs) are important for clinical cancer management. Here, we develop a fluid multivalent magnetic interface (FluidmagFace) in a microfluidic chip for high-performance isolation, release, and protein profiling of T-EVs. The FluidmagFace increases affinity by 105-fold with fluidity-enhanced multivalent binding to improve isolation efficiency by 13.9 % compared with a non-fluid interface. Its anti-adsorption property and microfluidic hydrodynamic shear minimize contamination, increasing detection sensitivity by two orders of magnitude. Moreover, its reversibility and expandability allow high-throughput recovery of T-EVs for mass spectrometric protein analysis. With the chip, T-EVs were detected in all tested cancer samples with identification of differentially expressed proteins compared with healthy controls. The FluidmagFace opens a new avenue to isolation and release of targets for cancer diagnosis and biomarker discovery.
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