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Engineering a subcellular targetable, red-emitting, and ratiometric fluorescent probe for Ca2+ and its bioimaging applications.工程化一种亚细胞靶向、红色发射、比率型荧光探针用于 Ca2+ 及其生物成像应用。
Anal Bioanal Chem. 2010 Jun;397(3):1245-50. doi: 10.1007/s00216-010-3650-7. Epub 2010 Mar 28.
2
High-speed tuning of visible laser wavelength using a nanoimprinted grating optical tunable filter.使用纳米压印光栅光学可调滤波器对可见激光波长进行高速调谐。
Appl Phys Lett. 2009 Nov 23;95(21):211106. doi: 10.1063/1.3267083. Epub 2009 Nov 24.
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Antibody-based protein multiplex platforms: technical and operational challenges.基于抗体的蛋白质多重检测平台:技术和操作挑战。
Clin Chem. 2010 Feb;56(2):186-93. doi: 10.1373/clinchem.2009.127514. Epub 2009 Dec 3.
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Imaging ligand-dependent activation of CXCR7.成像 CXCR7 配体依赖性激活。
Neoplasia. 2009 Oct;11(10):1022-35. doi: 10.1593/neo.09724.
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Hyperspectral image analysis of live cells in various cell cycle stages.不同细胞周期阶段活细胞的高光谱图像分析。
Cell Cycle. 2007 Oct 15;6(20):2563-70. doi: 10.4161/cc.6.20.4912. Epub 2007 Aug 21.
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Multispectral imaging in biology and medicine: slices of life.生物学与医学中的多光谱成像:生命切片
Cytometry A. 2006 Aug 1;69(8):748-58. doi: 10.1002/cyto.a.20319.
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Scanning microarrays: current methods and future directions.扫描微阵列:当前方法与未来方向。
Methods Enzymol. 2006;411:79-98. doi: 10.1016/S0076-6879(06)11006-X.
8
Quantitative measurement of nuclear translocation events using similarity analysis of multispectral cellular images obtained in flow.使用流动状态下获得的多光谱细胞图像的相似性分析对核转位事件进行定量测量。
J Immunol Methods. 2006 Apr 20;311(1-2):117-29. doi: 10.1016/j.jim.2006.01.018. Epub 2006 Mar 10.
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A guide to choosing fluorescent proteins.荧光蛋白选择指南。
Nat Methods. 2005 Dec;2(12):905-9. doi: 10.1038/nmeth819.
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Multiplexed microsphere assays for protein and DNA binding reactions.
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用于微流控彩色生物粒子流的多重光谱特征检测。

Multiplexed spectral signature detection for microfluidic color-coded bioparticle flow.

机构信息

Department of Mechanical Engineering, University of Michigan, Ann Arbor, 48109, United States.

出版信息

Anal Chem. 2010 Nov 15;82(22):9506-12. doi: 10.1021/ac102240g. Epub 2010 Oct 27.

DOI:10.1021/ac102240g
PMID:20979407
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2998408/
Abstract

Here, we report a high-speed photospectral detection technique capable of discriminating subtle variations of spectral signature among fluorescently labeled cells and microspheres flowing in a microfluidic channel. The key component used in our study is a strain-tunable nanoimprinted grating microdevice coupled with a photomultiplier tube (PMT). The microdevice permits acquisition of the continuous spectral profiles of multiple fluorescent emission sources at 1 kHz. Optically connected to a microfluidic flow chamber via a multimode optical fiber, our multiwavelength detection platform allows for cytometric measurement of cell groups emitting nearly identical fluorescence signals with a maximum emission wavelength difference as small as 5 nm. The same platform also allows us to demonstrate microfluidic flow cytometry of four different microsphere types in a wavelength bandwidth as narrow as 40 nm at a high (>85%) confidence level. Our study shows that detection of fluorescent spectral signatures at high speed and high resolution can expand specificity of multicolor flow cytometry. The enhanced capability enables multiplexed analysis of color-coded bioparticles based on single-laser excitation and single-detector spectroscopy in a microfluidic setting. The fluorescence signal discrimination power achieved by the optofluidic technology holds great promise to enable quantification of cellular parameters with higher accuracy as well as enumeration of a larger number of cell types than conventional flow cytometric methods.

摘要

在这里,我们报告了一种高速光光谱检测技术,该技术能够分辨在微流道中流动的荧光标记细胞和微球之间的光谱特征的细微变化。我们研究中使用的关键组件是一个应变可调谐的纳米压印光栅微器件,与光电倍增管(PMT)耦合。该微器件允许以 1 kHz 的频率采集多个荧光发射源的连续光谱曲线。通过多模光纤与微流控流室光学连接,我们的多波长检测平台允许对发射几乎相同荧光信号的细胞群体进行细胞计量测量,最大发射波长差小至 5nm。同一平台还使我们能够在高达 85%置信度的情况下,在 40nm 窄的波长带宽内,对四种不同类型的微球进行微流控流式细胞术检测。我们的研究表明,高速和高分辨率检测荧光光谱特征可以扩展多色流式细胞术的特异性。这种增强的功能使基于单激光激发和单探测器光谱学的彩色编码生物粒子的多路复用分析成为可能,在微流控环境中。光电流体技术实现的荧光信号分辨能力有望实现更高精度的细胞参数定量,以及比传统流式细胞术方法更大量的细胞类型计数。