Phasor-FSTM: a new paradigm for multicolor super-resolution imaging of living cells based on fluorescence modulation and lifetime multiplexing

IF 20.6 Q1 OPTICS
Luwei Wang, Yue Chen, Jiaqing Guo, Xiaoyu Weng, Wei Yan, Jun Song, Tong Ye, Junle Qu
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Abstract

Multicolor microscopy and super-resolution optical microscopy are two widely used techniques that greatly enhance the ability to distinguish and resolve structures in cellular imaging. These methods have individually transformed cellular imaging by allowing detailed visualization of cellular and subcellular structures, as well as organelle interactions. However, integrating multicolor and super-resolution microscopy into a single method remains challenging due to issues like spectral overlap, crosstalk, photobleaching, phototoxicity, and technical complexity. These challenges arise from the conflicting requirements of using different fluorophores for multicolor labeling and fluorophores with specific properties for super-resolution imaging. We propose a novel multicolor super-resolution imaging method called phasor-based fluorescence spatiotemporal modulation (Phasor-FSTM). This method uses time-resolved detection to acquire spatiotemporal data from encoded photons, employs phasor analysis to simultaneously separate multiple components, and applies fluorescence modulation to create super-resolution images. Phasor-FSTM enables the identification of multiple structural components with greater spatial accuracy on an enhanced laser scanning confocal microscope using a single-wavelength laser. To demonstrate the capabilities of Phasor-FSTM, we performed two-color to four-color super-resolution imaging at a resolution of ~λ/5 and observed the interactions of organelles in live cells during continuous imaging for a duration of over 20 min. Our method stands out for its simplicity and adaptability, seamlessly fitting into existing laser scanning microscopes without requiring multiple laser lines for excitation, which also provides a new avenue for other super-resolution imaging technologies based on different principles to build multi-color imaging systems with the requirement of a lower budget.

Abstract Image

相位fstm:基于荧光调制和寿命复用的活细胞多色超分辨率成像的新范式
多色显微镜和超分辨率光学显微镜是两种广泛使用的技术,它们极大地提高了细胞成像中结构的区分和分辨能力。这些方法通过允许细胞和亚细胞结构以及细胞器相互作用的详细可视化,分别改变了细胞成像。然而,由于光谱重叠、串扰、光漂白、光毒性和技术复杂性等问题,将多色和超分辨率显微镜集成到单一方法中仍然具有挑战性。这些挑战来自使用不同的荧光团进行多色标记和使用具有特定属性的荧光团进行超分辨率成像的相互冲突的要求。我们提出了一种新的多色超分辨率成像方法——基于相量的荧光时空调制(Phasor-FSTM)。该方法利用时间分辨检测从编码光子中获取时空数据,利用相量分析同时分离多个分量,并利用荧光调制创建超分辨率图像。相位fstm使识别多个结构部件具有更高的空间精度在增强激光扫描共聚焦显微镜使用单波长激光。为了证明相位fstm的能力,我们在~λ/5的分辨率下进行了双色到四色的超分辨率成像,并在持续超过20分钟的连续成像期间观察了活细胞中细胞器的相互作用。该方法具有简单、适应性强的特点,无需多条激光线进行激发即可无缝适配现有的激光扫描显微镜,这也为其他基于不同原理的超分辨率成像技术以更低的预算要求构建多色成像系统提供了新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Light-Science & Applications
Light-Science & Applications 数理科学, 物理学I, 光学, 凝聚态物性 II :电子结构、电学、磁学和光学性质, 无机非金属材料, 无机非金属类光电信息与功能材料, 工程与材料, 信息科学, 光学和光电子学, 光学和光电子材料, 非线性光学与量子光学
自引率
0.00%
发文量
803
审稿时长
2.1 months
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