A sandwiched photoelectrochemical sensor for high-throughput single-cell analysis based on low-toxic and near-infrared AgInS2 microarray

单细胞分析 微电极 光电流 聚二甲基硅氧烷 化学 基质(水族馆) 多电极阵列 纳米技术 分析物 材料科学 细胞 生物物理学 光电子学 色谱法 电极 生物化学 物理化学 地质学 海洋学 生物
作者
Lin Zhong,Kejun Guo,Li Su,Juan Wang
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:470: 144137-144137 被引量:5
标识
DOI:10.1016/j.cej.2023.144137
摘要

High-throughput single-cell quantitative analysis is becoming increasingly important to elucidate cellular heterogeneity and further understand some related disease mechanisms. Various techniques including mass spectrometry, fluorescence detection, and electrochemiluminescence analysis have made significant progress in this area, but their dilemma is the destruction of cellular activity, the introduction of exogenetic probes and the resulting cellular metabolism perturbation, or the steric hindrance of the cells to the substrate. Here, we develop a non-destructive, probe-free, and hindrance-free photoelectrochemical (PEC) single-cell microsensor. First, a patterned PEC microelectrode with low-toxic and near-infrared AgInS2 microdots is simply fabricated by using a polydimethylsiloxane (PDMS) microstencil, exhibiting high photoelectric efficiency and low S2- detection limit (1.0 nM). Then, a PDMS microwell array is prepared for single cells trapping, matching the size of the microelectrode and with high single-cell occupancy (>93%). Finally, a sealed sandwiching platform is formed by aligning and clamping the two arrays, each microdot contacts with a single cell in one microwell and reacts with the secreted H2S, preventing the neighboring microwell’s cross-contamination, cellular analyte’s dilution, and cell’s steric effect. The different light-addressable recorded photocurrent signals of all single cells directly reflect the 55.6% cell-to-cell differences. This report provides a useful and powerful tool to study single-cell heterogeneity.
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