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Journal of Biomedical Optics最新文献

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Deep learning-based spectroscopic single-molecule localization microscopy 基于深度学习的光谱单分子定位显微技术
Pub Date : 2024-05-24 DOI: 10.1117/1.JBO.29.6.066501
Sunil Kumar Gaire, A. Daneshkhah, Ethan Flowerday, Ruyi Gong, J. Frederick, Vadim Backman
Abstract. Significance Spectroscopic single-molecule localization microscopy (sSMLM) takes advantage of nanoscopy and spectroscopy, enabling sub-10 nm resolution as well as simultaneous multicolor imaging of multi-labeled samples. Reconstruction of raw sSMLM data using deep learning is a promising approach for visualizing the subcellular structures at the nanoscale. Aim Develop a novel computational approach leveraging deep learning to reconstruct both label-free and fluorescence-labeled sSMLM imaging data. Approach We developed a two-network-model based deep learning algorithm, termed DsSMLM, to reconstruct sSMLM data. The effectiveness of DsSMLM was assessed by conducting imaging experiments on diverse samples, including label-free single-stranded DNA (ssDNA) fiber, fluorescence-labeled histone markers on COS-7 and U2OS cells, and simultaneous multicolor imaging of synthetic DNA origami nanoruler. Results For label-free imaging, a spatial resolution of 6.22 nm was achieved on ssDNA fiber; for fluorescence-labeled imaging, DsSMLM revealed the distribution of chromatin-rich and chromatin-poor regions defined by histone markers on the cell nucleus and also offered simultaneous multicolor imaging of nanoruler samples, distinguishing two dyes labeled in three emitting points with a separation distance of 40 nm. With DsSMLM, we observed enhanced spectral profiles with 8.8% higher localization detection for single-color imaging and up to 5.05% higher localization detection for simultaneous two-color imaging. Conclusions We demonstrate the feasibility of deep learning-based reconstruction for sSMLM imaging applicable to label-free and fluorescence-labeled sSMLM imaging data. We anticipate our technique will be a valuable tool for high-quality super-resolution imaging for a deeper understanding of DNA molecules’ photophysics and will facilitate the investigation of multiple nanoscopic cellular structures and their interactions.
摘要意义 光谱单分子定位显微镜(sSMLM)利用纳米镜和光谱学的优势,实现了 10 纳米以下的分辨率以及多标记样品的同步多色成像。利用深度学习重构原始 sSMLM 数据是实现纳米尺度亚细胞结构可视化的一种可行方法。目标 开发一种利用深度学习重建无标记和荧光标记 sSMLM 成像数据的新型计算方法。方法 我们开发了一种基于双网络模型的深度学习算法,称为 DsSMLM,用于重建 sSMLM 数据。通过对不同样本进行成像实验,评估了 DsSMLM 的有效性,包括无标记的单链 DNA(ssDNA)纤维、COS-7 和 U2OS 细胞上荧光标记的组蛋白标记物,以及合成 DNA 纳米折纸的同步多色成像。结果 在无标记成像中,ssDNA 纤维的空间分辨率达到了 6.22 nm;在荧光标记成像中,DsSMLM 揭示了细胞核上组蛋白标记所定义的染色质富集区和染色质贫乏区的分布情况,还提供了纳米尺样品的同步多色成像,可在三个发射点上以 40 nm 的间距区分两种染料标记。利用 DsSMLM,我们观察到光谱轮廓得到了增强,单色成像的定位检测率提高了 8.8%,同步双色成像的定位检测率提高了 5.05%。结论 我们证明了基于深度学习的 sSMLM 成像重建适用于无标记和荧光标记 sSMLM 成像数据的可行性。我们预计,我们的技术将成为高质量超分辨率成像的重要工具,以加深对 DNA 分子光物理的理解,并促进对多种纳米细胞结构及其相互作用的研究。
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Journal of Biomedical Optics
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