Tunable Single-Cell Extraction for Molecular Analyses

被引:134
作者
Guillaume-Gentil, Orane [1 ]
Grindberg, Rashel V. [1 ]
Kooger, Romain [2 ]
Dorwling-Carter, Livie [3 ]
Martinez, Vincent [3 ]
Ossola, Dario [3 ]
Pilhofer, Martin [2 ]
Zambelli, Tomaso [3 ]
Vorholt, Julia A. [1 ]
机构
[1] ETH, Inst Microbiol, Dept Biol, CH-8093 Zurich, Switzerland
[2] ETH, Inst Mol Biol & Biophys, Dept Biol, CH-8093 Zurich, Switzerland
[3] ETH, Inst Biomed Engn, Lab Biosensors & Bioelect, CH-8092 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
RNA-SEQ; GENE-EXPRESSION; PROTEINS; INHIBITOR; FLUIDFM; GENOME; ARRAYS;
D O I
10.1016/j.cell.2016.06.025
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Because of cellular heterogeneity, the analysis of endogenous molecules from single cells is of significant interest and has major implications. While micromanipulation or cell sorting followed by cell lysis is already used for subsequent molecular examinations, approaches to directly extract the content of living cells remain a challenging but promising alternative to achieving non-destructive sampling and cell-context preservation. Here, we demonstrate the quantitative extraction from single cells with spatiotemporal control using fluidic force microscopy. We further present a comprehensive analysis of the soluble molecules withdrawn from the cytoplasm or the nucleus, including the detection of enzyme activities and transcript abundances. This approach has uncovered the ability of cells to withstand extraction of up to several picoliters and opens opportunities to study cellular dynamics and cell-cell communication under physiological conditions at the single-cell level.
引用
收藏
页码:506 / 516
页数:11
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