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新型 PE 和 APC 串联:用于光谱流式细胞术的额外近红外荧光染料。

Novel PE and APC tandems: Additional near-infrared fluorochromes for use in spectral flow cytometry.

机构信息

AbbVie Biotherapeutics, AbbVie Inc., South San Francisco, California, USA.

Former AbbVie Employee.

出版信息

Cytometry A. 2022 Oct;101(10):835-845. doi: 10.1002/cyto.a.24537. Epub 2022 Feb 2.

DOI:10.1002/cyto.a.24537
PMID:35112484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9790705/
Abstract

Recent advances in flow cytometry instrumentation and fluorochrome chemistries have greatly increased fluorescent conjugated antibody combinations that can be used reliably and easily in routine experiments. The Cytek Aurora flow cytometer was first released with three excitation lasers (405, 488, and 640 nm) and incorporated the latest Avalanche Photodiode (APD) technology, demonstrating significant improvement in sensitivity for fluorescent emission signals longer than 800 nm. However, there are limited commercially available fluorochromes capable of excitation with peak emission signals beyond 800 nm. To address this gap, we engineered six new fluorochromes: PE-750, PE-800, PE-830 for the 488 nm laser and APC-750, APC-800, APC-830 for the 640 nm laser. Utilizing the principal of fluorescence resonance energy transfer (FRET), these novel structures were created by covalently linking a protein donor dye with an organic small molecule acceptor dye. Additionally, each of these fluorochrome conjugates were shown to be compatible with fixation/permeabilization buffer reagents, and demonstrated acceptable brightness and stability when conjugated to antigen-specific monoclonal antibodies. These six novel fluorochrome reagents can increase the numbers of fluorochromes that can be used on a spectral flow cytometer.

摘要

近年来,流式细胞仪仪器和荧光染料化学的进步极大地增加了荧光偶联抗体的组合,可以可靠且轻松地用于常规实验。Cytek Aurora 流式细胞仪最初配备了三个激发激光器(405nm、488nm 和 640nm),并采用了最新的雪崩光电二极管 (APD) 技术,对长于 800nm 的荧光发射信号的灵敏度有了显著提高。然而,能够用峰值发射信号激发的商业上可用的荧光染料数量有限。为了解决这一差距,我们设计了六种新型荧光染料:PE-750、PE-800、PE-830 用于 488nm 激光,APC-750、APC-800、APC-830 用于 640nm 激光。利用荧光共振能量转移 (FRET) 的原理,通过将蛋白质供体染料与有机小分子受体染料共价连接,形成这些新型结构。此外,这些荧光染料与固定/透化缓冲试剂兼容,并且当与抗原特异性单克隆抗体偶联时,表现出可接受的亮度和稳定性。这六种新型荧光染料试剂可以增加光谱流式细胞仪上可使用的荧光染料数量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/e3bdfd84a4e7/CYTO-101-835-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/ab6edfafa51c/CYTO-101-835-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/5621981fffed/CYTO-101-835-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/09702c2c6e73/CYTO-101-835-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/1abb3e772054/CYTO-101-835-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/e3bdfd84a4e7/CYTO-101-835-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/ab6edfafa51c/CYTO-101-835-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/5621981fffed/CYTO-101-835-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/09702c2c6e73/CYTO-101-835-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/1abb3e772054/CYTO-101-835-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2783/9790705/e3bdfd84a4e7/CYTO-101-835-g005.jpg

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Cytometry A. 2020 Oct;97(10):1044-1051. doi: 10.1002/cyto.a.24213. Epub 2020 Aug 31.
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Panel Design and Optimization for High-Dimensional Immunophenotyping Assays Using Spectral Flow Cytometry.使用光谱流式细胞术进行高维免疫表型分析的面板设计和优化。
Curr Protoc Cytom. 2020 Mar;92(1):e70. doi: 10.1002/cpcy.70.
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Recent Advances in Bioorthogonal Click Chemistry for Efficient Synthesis of Radiotracers and Radiopharmaceuticals.
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Molecules. 2019 Oct 2;24(19):3567. doi: 10.3390/molecules24193567.
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Novel full-spectral flow cytometry with multiple spectrally-adjacent fluorescent proteins and fluorochromes and visualization of in vivo cellular movement.具有多种光谱相邻荧光蛋白和荧光染料的新型全光谱流式细胞术以及体内细胞运动的可视化
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Quantifying spillover spreading for comparing instrument performance and aiding in multicolor panel design.量化溢出扩散,用于比较仪器性能并辅助多色面板设计。
Cytometry A. 2013 Mar;83(3):306-15. doi: 10.1002/cyto.a.22251. Epub 2013 Feb 6.
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