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量子点编码微珠

Quantum dot-encoded beads.

作者信息

Gao Xiaohu, Nie Shuming

机构信息

Department of Biomedical Engineering, Emory University, Atlanta, GA, USA.

出版信息

Methods Mol Biol. 2005;303:61-71. doi: 10.1385/1-59259-901-X:061.

Abstract

Multicolor optical coding for biological assays has been achieved by embedding semiconductor quantum dots into mesoporous and macroporous beads at precisely controlled ratios. Owing to their novel optical properties such as size-tunable emission and simultaneous excitation, quantum dots are ideal fluorophores for wavelength-and-intensity multiplexing. Kinetics study reveals that quantum dot doping of porous silica and polystyrene beads can be completed from seconds to minutes. The use of 10 intensity levels and six colors could theoretically code 1 million nucleic acid or protein sequences. Imaging and spectroscopic measurements indicate that the quantum dot-tagged beads are highly uniform and reproducible, yielding bead identification accuracies as high as 99.99% under favorable conditions. DNA hybridization studies demonstrate that the coding and target signals can be simultaneously read at the single-bead level. This spectral coding technology is expected to open new opportunities in gene expression studies, high-throughput screening, and medical diagnostics.

摘要

通过将半导体量子点以精确控制的比例嵌入介孔和大孔微珠中,实现了用于生物分析的多色光学编码。由于量子点具有诸如发射波长可调谐和同时激发等新颖的光学特性,它们是用于波长和强度复用的理想荧光团。动力学研究表明,多孔二氧化硅和聚苯乙烯微珠的量子点掺杂可在数秒到数分钟内完成。使用10个强度级别和六种颜色理论上可以编码100万个核酸或蛋白质序列。成像和光谱测量表明,量子点标记的微珠高度均匀且可重复,在有利条件下微珠识别准确率高达99.99%。DNA杂交研究表明,可以在单微珠水平上同时读取编码信号和目标信号。这种光谱编码技术有望在基因表达研究、高通量筛选和医学诊断中开辟新的机遇。

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