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微球中单色荧光各向异性条形码的扩展用于多重生化检测。

Expanded single-color barcoding in microspheres with fluorescence anisotropy for multiplexed biochemical detection.

机构信息

Department of Chemistry, Southern University of Science and Technology, Shenzhen, 518055, China.

Academy for Advanced Interdisciplinary Studies, Southern University of Science and Technology, Shenzhen, 518055, China.

出版信息

Analyst. 2023 Sep 11;148(18):4406-4413. doi: 10.1039/d3an00938f.

Abstract

Single-color barcoding strategies could break the limits of spectral crosstalk in conventional intensity-based fluorescence barcodes. Fluorescence anisotropy (FA), a self-referencing quantity able to differentiate spectrally similar fluorophores, is highly attractive in designing fluorescent barcodes within a limited emission window. In this study, FA-based encoding of polystyrene (PS) microspheres was realized for the first time. The FA signals of fluorophores were stabilized inside PS microspheres owing to hampered rotational motion. Fluorescent labels were incorporated with similar emission but different structures, symmetries, and lifetimes. On the one hand, Förster Resonance Energy Transfer (FRET) including homo-FRET and hetero-FRET resulted in a decrease of steady-state FA with increasing dye loading, converting conventional intensity-based codes into FA-based codes. On the other hand, mixing dyes with different intrinsic FA values generated different FA values at the same fluorescence intensity level. Single color 5-plex FA-encoded microspheres were demonstrated and decoded on a homemade microscopic FA imaging platform in real time. The FA-encoded microspheres were successfully applied to detect the oligonucleotide of the foodborne bacterium, , without spectral crosstalk between the encoding and reporting dyes. Overall, FA-based encoding with an expanded coding capacity in the FA dimension holds great potential in multiplexed high-throughput chemical and biological analyses.

摘要

单颜色编码策略可以打破传统强度荧光条码中光谱串扰的限制。荧光各向异性(FA)是一种能够区分光谱相似荧光团的自参考量,在设计有限发射窗口内的荧光条码时非常有吸引力。在本研究中,首次实现了基于 FA 的聚苯乙烯(PS)微球编码。由于旋转运动受阻,荧光染料的 FA 信号在 PS 微球内部得到稳定。荧光标记物具有相似的发射但不同的结构、对称性和寿命。一方面,包括同分子内Förster 共振能量转移(FRET)和异分子内 FRET 的 FRET 导致稳态 FA 随着染料负载量的增加而降低,从而将传统的基于强度的编码转换为基于 FA 的编码。另一方面,混合具有不同固有 FA 值的染料在相同荧光强度水平下产生不同的 FA 值。单颜色 5 重 FA 编码微球在自制的微观 FA 成像平台上实时进行了演示和解码。FA 编码微球成功应用于检测食源性细菌的寡核苷酸,而不会发生编码和报告染料之间的光谱串扰。总体而言,FA 编码具有扩展的 FA 维度编码容量,在多路复用高通量化学和生物分析中具有巨大潜力。

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