用于流式细胞仪的深紫外 266 纳米激光激发。

IF 2.5 4区 生物学 Q3 BIOCHEMICAL RESEARCH METHODS Cytometry Part A Pub Date : 2023-12-20 DOI:10.1002/cyto.a.24813
William Telford
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引用次数: 0

摘要

高维流式细胞仪依靠多个激光源来激发目前可用于免疫分型的各种荧光染料。紫外激光器(通常为固态 355 纳米)是其中的关键部分,因为它们能激发 BD Horizon™ Brilliant Ultraviolet (BUV) 系列聚合物荧光染料。BUV 染料将可用于实际高维分析的同步荧光染料数量增加到了 40 多种,可用于光谱 cytometry。免疫学家现在正努力增加这一数量,这需要新型荧光染料和更多的激光波长。目前正在开发更多具有深紫外(DUV)激发光源的聚合物染料,在此推动下,深紫外(DUV)范围(约 260 至 320 纳米)的激光已被提议作为额外的激发光源。波长为 280 和 320 nm 的 DUV 激光器已在流式细胞仪中得到验证,但在探针激发行为和可用性方面都遇到了实际困难。在本文中,我们验证了用于流式细胞仪的波长更短的 266 纳米 DUV 激光源。这种 DUV 激光对 BUV 染料的激发极小(这是高维分析的理想特性),同时对作为尚未开发的 DUV 激发染料的替代荧光素的量子纳米粒子(Qdots)的激发效果极佳。因此,DUV 266 nm 激发可能是将高维流式细胞仪扩展到 DUV 范围的可行候选方法,并为光谱细胞仪提供额外的附带激发波长。在核酸和蛋白质吸收较强的光谱区域(260-280 nm)进行激发确实会产生较强的自发荧光,这就要求在选择荧光色素时小心谨慎。不过,DUV 激发内源分子可能会在无标记分析应用中发挥更大的作用。
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Deep ultraviolet 266 nm laser excitation for flow cytometry

High dimensional flow cytometry relies on multiple laser sources to excite the wide variety of fluorochromes now available for immunophenotyping. Ultraviolet lasers (usually solid state 355 nm) are a critical part of this as they excite the BD Horizon™ Brilliant Ultraviolet (BUV) series of polymer fluorochromes. The BUV dyes have increased the number of simultaneous fluorochromes available for practical high-dimensional analysis to greater than 40 for spectral cytometry. Immunologists are now seeking to increase this number, requiring both novel fluorochromes and additional laser wavelengths. A laser in the deep ultraviolet (DUV) range (from ca. 260 to 320 nm) has been proposed as an additional excitation source, driven by the on-going development of additional polymer dyes with DUV excitation. DUV lasers emitting at 280 and 320 nm have been previously validated for flow cytometry but have encountered practical difficulties both in probe excitation behavior and in availability. In this article, we validate an even shorter DUV 266 nm laser source for flow cytometry. This DUV laser provided minimal excitation of the BUV dyes (a desirable characteristic for high-dimensional analysis) while demonstrating excellent excitation of quantum nanoparticles (Qdots) serving as surrogate fluorochromes for as yet undeveloped DUV excited dyes. DUV 266 nm excitation may therefore be a viable candidate for expanding high-dimensional flow cytometry into the DUV range and providing an additional incidental excitation wavelength for spectral cytometry. Excitation in a spectral region with strong absorption by nucleic acids and proteins (260–280 nm) did result in strong autofluorescence requiring care in fluorochrome selection. DUV excitation of endogenous molecules may nevertheless have additional utility for label-free analysis applications.

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来源期刊
Cytometry Part A
Cytometry Part A 生物-生化研究方法
CiteScore
8.10
自引率
13.50%
发文量
183
审稿时长
4-8 weeks
期刊介绍: Cytometry Part A, the journal of quantitative single-cell analysis, features original research reports and reviews of innovative scientific studies employing quantitative single-cell measurement, separation, manipulation, and modeling techniques, as well as original articles on mechanisms of molecular and cellular functions obtained by cytometry techniques. The journal welcomes submissions from multiple research fields that fully embrace the study of the cytome: Biomedical Instrumentation Engineering Biophotonics Bioinformatics Cell Biology Computational Biology Data Science Immunology Parasitology Microbiology Neuroscience Cancer Stem Cells Tissue Regeneration.
期刊最新文献
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