通过空间光谱优化的图像干涉结构照明显微镜提高高保真各向同性超分辨率

IF 9.8 1区 物理与天体物理 Q1 OPTICS
Enxing He, Yile Sun, Hongfei Zhu, Xinxun Yang, Lu Yin, Yubing Han, Cuifang Kuang, Xu Liu
{"title":"通过空间光谱优化的图像干涉结构照明显微镜提高高保真各向同性超分辨率","authors":"Enxing He, Yile Sun, Hongfei Zhu, Xinxun Yang, Lu Yin, Yubing Han, Cuifang Kuang, Xu Liu","doi":"10.1002/lpor.202500178","DOIUrl":null,"url":null,"abstract":"Spatial resolution is crucial for imaging subcellular structures. The advent of three‐dimensional structured illumination microscopy (3D‐SIM) greatly benefits the biology community, providing a powerful tool for imaging organelles with a twofold resolution enhancement in all three dimensions. However, the axial resolution of 3D‐SIM is limited to around 300 nm, which is inferior to its lateral resolution. Here, a novel method called image interference SIM () is reported, which utilizes two oppositely positioned objectives to detect fluorescence emission interference under three‐beam excitation. By incorporating spectral modulation and spatial domain Frobenius‐Hessian optimization, achieves an axial resolution approximately twice that of 3D‐SIM, reaching around 130 nm. Furthermore, the potential of for imaging subcellular structures is demonstrated on various biological samples, including microtubules, actin filaments, and mitochondrial outer membranes. The enhanced optical sectioning capability can be utilized to resolve axial structures that are challenging to discern using ordinary 3D‐SIM.","PeriodicalId":204,"journal":{"name":"Laser & Photonics Reviews","volume":"25 1","pages":""},"PeriodicalIF":9.8000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Boosting High‐Fidelity Isotropic Super‐Resolution via Image Interference Structured Illumination Microscopy with Spatial‐Spectral Optimization\",\"authors\":\"Enxing He, Yile Sun, Hongfei Zhu, Xinxun Yang, Lu Yin, Yubing Han, Cuifang Kuang, Xu Liu\",\"doi\":\"10.1002/lpor.202500178\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Spatial resolution is crucial for imaging subcellular structures. The advent of three‐dimensional structured illumination microscopy (3D‐SIM) greatly benefits the biology community, providing a powerful tool for imaging organelles with a twofold resolution enhancement in all three dimensions. However, the axial resolution of 3D‐SIM is limited to around 300 nm, which is inferior to its lateral resolution. Here, a novel method called image interference SIM () is reported, which utilizes two oppositely positioned objectives to detect fluorescence emission interference under three‐beam excitation. By incorporating spectral modulation and spatial domain Frobenius‐Hessian optimization, achieves an axial resolution approximately twice that of 3D‐SIM, reaching around 130 nm. Furthermore, the potential of for imaging subcellular structures is demonstrated on various biological samples, including microtubules, actin filaments, and mitochondrial outer membranes. The enhanced optical sectioning capability can be utilized to resolve axial structures that are challenging to discern using ordinary 3D‐SIM.\",\"PeriodicalId\":204,\"journal\":{\"name\":\"Laser & Photonics Reviews\",\"volume\":\"25 1\",\"pages\":\"\"},\"PeriodicalIF\":9.8000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Laser & Photonics Reviews\",\"FirstCategoryId\":\"101\",\"ListUrlMain\":\"https://doi.org/10.1002/lpor.202500178\",\"RegionNum\":1,\"RegionCategory\":\"物理与天体物理\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"OPTICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Laser & Photonics Reviews","FirstCategoryId":"101","ListUrlMain":"https://doi.org/10.1002/lpor.202500178","RegionNum":1,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"OPTICS","Score":null,"Total":0}
引用次数: 0

摘要

空间分辨率是成像亚细胞结构的关键。三维结构照明显微镜(3D - SIM)的出现极大地造福了生物界,为成像细胞器提供了一个强大的工具,在所有三个维度上具有两倍的分辨率增强。然而,3D‐SIM的轴向分辨率限制在300 nm左右,低于其横向分辨率。本文报道了一种称为图像干涉SIM()的新方法,该方法利用两个相对位置的物镜来检测三束激发下的荧光发射干扰。通过结合光谱调制和空间域Frobenius - Hessian优化,实现了大约两倍于3D - SIM的轴向分辨率,达到约130 nm。此外,亚细胞结构成像的潜力在各种生物样品上得到了证明,包括微管、肌动蛋白丝和线粒体外膜。增强的光学切片能力可用于解决轴向结构,这是使用普通3D‐SIM难以识别的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Boosting High‐Fidelity Isotropic Super‐Resolution via Image Interference Structured Illumination Microscopy with Spatial‐Spectral Optimization
Spatial resolution is crucial for imaging subcellular structures. The advent of three‐dimensional structured illumination microscopy (3D‐SIM) greatly benefits the biology community, providing a powerful tool for imaging organelles with a twofold resolution enhancement in all three dimensions. However, the axial resolution of 3D‐SIM is limited to around 300 nm, which is inferior to its lateral resolution. Here, a novel method called image interference SIM () is reported, which utilizes two oppositely positioned objectives to detect fluorescence emission interference under three‐beam excitation. By incorporating spectral modulation and spatial domain Frobenius‐Hessian optimization, achieves an axial resolution approximately twice that of 3D‐SIM, reaching around 130 nm. Furthermore, the potential of for imaging subcellular structures is demonstrated on various biological samples, including microtubules, actin filaments, and mitochondrial outer membranes. The enhanced optical sectioning capability can be utilized to resolve axial structures that are challenging to discern using ordinary 3D‐SIM.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
14.20
自引率
5.50%
发文量
314
审稿时长
2 months
期刊介绍: Laser & Photonics Reviews is a reputable journal that publishes high-quality Reviews, original Research Articles, and Perspectives in the field of photonics and optics. It covers both theoretical and experimental aspects, including recent groundbreaking research, specific advancements, and innovative applications. As evidence of its impact and recognition, Laser & Photonics Reviews boasts a remarkable 2022 Impact Factor of 11.0, according to the Journal Citation Reports from Clarivate Analytics (2023). Moreover, it holds impressive rankings in the InCites Journal Citation Reports: in 2021, it was ranked 6th out of 101 in the field of Optics, 15th out of 161 in Applied Physics, and 12th out of 69 in Condensed Matter Physics. The journal uses the ISSN numbers 1863-8880 for print and 1863-8899 for online publications.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信