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基于噬菌体的纳米颗粒导向捕获技术对稀有单细胞进行分析。

Phage-Based Profiling of Rare Single Cells Using Nanoparticle-Directed Capture.

机构信息

Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario M5S 3M2, Canada.

State Key Laboratory of Tribology, Tsinghua University, Beijing 100084, P.R. China.

出版信息

ACS Nano. 2021 Dec 28;15(12):19202-19210. doi: 10.1021/acsnano.1c03935. Epub 2021 Nov 23.

Abstract

Advances in single-cell level profiling of the proteome require quantitative and versatile platforms, especially for rare cell analyses such as circulating tumor cell (CTC) profiling. Here we demonstrate an integrated microfluidic chip that uses magnetic nanoparticles to capture single tumor cells with high efficiency, permits on-chip incubation, and facilitates cell-surface protein expression analysis. Combined with phage-based barcoding and next-generation sequencing technology, we were able to monitor changes in the expression of multiple surface markers stimulated in response to CTC adherence. Interestingly, we found fluctuations in the expression of Frizzled2 (FZD2) that reflected the microenvironment of the single cells. This platform has a high potential for in-depth screening of multiple surface antigens simultaneously in rare cells with single-cell resolution, which will provide further insights regarding biological heterogeneity and human disease.

摘要

单细胞水平蛋白质组分析需要定量且多功能的平台,特别是对于循环肿瘤细胞(CTC)分析等稀有细胞分析。在这里,我们展示了一种集成的微流控芯片,该芯片使用磁性纳米颗粒高效捕获单个肿瘤细胞,允许在芯片上孵育,并便于细胞表面蛋白表达分析。结合基于噬菌体的条形码和下一代测序技术,我们能够监测到响应 CTC 附着而刺激的多个表面标记物表达的变化。有趣的是,我们发现卷曲蛋白 2(FZD2)的表达波动反映了单个细胞的微环境。该平台具有在稀有细胞中以单细胞分辨率同时对多个表面抗原进行深入筛选的巨大潜力,这将为生物异质性和人类疾病提供更深入的了解。

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