• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

快速非线性图像扫描显微镜。

Rapid nonlinear image scanning microscopy.

机构信息

3rd Institute of Physics - Biophysics, University of Göttingen, Göttingen, Germany.

Center for Nanoscale Microscopy and Molecular Physiology of the Brain (CNMPB), Göttingen, Germany.

出版信息

Nat Methods. 2017 Nov;14(11):1087-1089. doi: 10.1038/nmeth.4467. Epub 2017 Oct 16.

DOI:10.1038/nmeth.4467
PMID:29039418
Abstract

Image scanning microscopy (ISM) doubles the resolution of a conventional confocal microscope for super-resolution imaging. Here, we describe an all-optical ISM design based on rescanning microscopy for two-photon-excited fluorescence and second-harmonic generation that allows straightforward implementation into existing microscopes. The design offers improved sensitivity and high frame rates relative to those of existing systems. We demonstrate its utility using fixed and living specimens as well as collagen hydrogels.

摘要

图像扫描显微镜(ISM)将传统共聚焦显微镜的分辨率提高了一倍,可用于超分辨率成像。本文描述了一种基于重扫描显微镜的全光学 ISM 设计,用于双光子激发荧光和二次谐波产生,可直接集成到现有显微镜中。与现有系统相比,该设计具有更高的灵敏度和更高的帧率。我们使用固定和活的样本以及胶原水凝胶证明了其效用。

相似文献

1
Rapid nonlinear image scanning microscopy.快速非线性图像扫描显微镜。
Nat Methods. 2017 Nov;14(11):1087-1089. doi: 10.1038/nmeth.4467. Epub 2017 Oct 16.
2
Effect of a confocal pinhole in two-photon microscopy.共聚焦针孔在双光子显微镜中的作用。
Microsc Res Tech. 1999 Nov 1;47(3):210-4. doi: 10.1002/(SICI)1097-0029(19991101)47:3<210::AID-JEMT7>3.0.CO;2-H.
3
A robust and versatile platform for image scanning microscopy enabling super-resolution FLIM.用于图像扫描显微镜的强大且多功能平台,可实现超分辨率 FLIM。
Nat Methods. 2019 Feb;16(2):175-178. doi: 10.1038/s41592-018-0291-9. Epub 2019 Jan 14.
4
Image scanning microscopy.图像扫描显微镜。
Curr Opin Chem Biol. 2019 Aug;51:74-83. doi: 10.1016/j.cbpa.2019.05.011. Epub 2019 Jun 13.
5
Doubling the resolution of a confocal spinning-disk microscope using image scanning microscopy.利用图像扫描显微镜将共聚焦旋转盘显微镜的分辨率提高一倍。
Nat Protoc. 2021 Jan;16(1):164-181. doi: 10.1038/s41596-020-00408-x. Epub 2020 Nov 27.
6
Resolution doubling in fluorescence microscopy with confocal spinning-disk image scanning microscopy.荧光显微镜中的分辨率提高两倍,采用共聚焦旋转盘图像扫描显微镜。
Proc Natl Acad Sci U S A. 2013 Dec 24;110(52):21000-5. doi: 10.1073/pnas.1315858110. Epub 2013 Dec 9.
7
Improvement of image resolution by combining enhanced confocal microscopy and quantum dot triexciton imaging.通过结合增强共焦显微镜和量子点三体激子成像来提高图像分辨率。
FEBS Open Bio. 2021 Dec;11(12):3324-3330. doi: 10.1002/2211-5463.13246. Epub 2021 Jul 26.
8
Minimizing light exposure with the programmable array microscope.利用可编程阵列显微镜减少光暴露。
J Microsc. 2011 Jan;241(1):101-10. doi: 10.1111/j.1365-2818.2010.03413.x.
9
Saturated-excitation image scanning microscopy.饱和激发成像显微镜。
Opt Express. 2022 Apr 11;30(8):13825-13838. doi: 10.1364/OE.455621.
10
Practical limits of resolution in confocal and non-linear microscopy.共聚焦和非线性显微镜中分辨率的实际限制。
Microsc Res Tech. 2004 Jan 1;63(1):18-22. doi: 10.1002/jemt.10423.

引用本文的文献

1
Super-resolution upgrade for deep tissue imaging featuring simple implementation.用于深度组织成像的超分辨率升级,具有简单的实现方式。
Nat Commun. 2025 Jun 25;16(1):5386. doi: 10.1038/s41467-025-60744-y.
2
Transparent, metal-free PEDOT:PSS neural interfaces for simultaneous recording of low-noise electrophysiology and artifact-free two-photon imaging.用于同时记录低噪声电生理学和无伪影双光子成像的透明、无金属聚(3,4-乙撑二氧噻吩):聚苯乙烯磺酸盐神经接口。
Nat Commun. 2025 Apr 29;16(1):4032. doi: 10.1038/s41467-025-59303-2.
3
Fluorescent labeling strategies for molecular bioimaging.

本文引用的文献

1
In vivo three-photon imaging of activity of GCaMP6-labeled neurons deep in intact mouse brain.在完整小鼠大脑深处用 GCaMP6 标记的神经元的体内三光子成像。
Nat Methods. 2017 Apr;14(4):388-390. doi: 10.1038/nmeth.4183. Epub 2017 Feb 20.
2
High-resolution confocal Raman microscopy using pixel reassignment.使用像素重新分配的高分辨率共聚焦拉曼显微镜。
Opt Lett. 2016 Aug 15;41(16):3825-8. doi: 10.1364/OL.41.003825.
3
Superconcentration of light: circumventing the classical limit to achievable irradiance.光的超聚焦:突破可实现辐照度的经典极限。
用于分子生物成像的荧光标记策略。
Biophys Rep (N Y). 2025 Mar 12;5(1):100200. doi: 10.1016/j.bpr.2025.100200. Epub 2025 Feb 12.
4
Super-resolved coherent anti-Stokes Raman scattering microscopy by coherent image scanning.通过相干图像扫描实现的超分辨相干反斯托克斯拉曼散射显微镜技术
Nat Commun. 2024 Nov 21;15(1):10073. doi: 10.1038/s41467-024-54429-1.
5
Widefield polarization-resolved second harmonic generation imaging of entire thyroid nodule sections for the detection of capsular invasion.用于检测包膜侵犯的全甲状腺结节切片宽场偏振分辨二次谐波生成成像
Biomed Opt Express. 2024 Jul 17;15(8):4705-4718. doi: 10.1364/BOE.523052. eCollection 2024 Aug 1.
6
Roadmap on Label-Free Super-Resolution Imaging.无标记超分辨率成像路线图
Laser Photon Rev. 2023 Dec;17(12). doi: 10.1002/lpor.202200029. Epub 2023 Oct 30.
7
Toward next-generation endoscopes integrating biomimetic video systems, nonlinear optical microscopy, and deep learning.迈向集成仿生视频系统、非线性光学显微镜和深度学习的下一代内窥镜。
Biophys Rev (Melville). 2023 Jun 29;4(2):021307. doi: 10.1063/5.0133027. eCollection 2023 Jun.
8
Superresolution structured illumination microscopy reconstruction algorithms: a review.超分辨率结构光照明显微镜重建算法综述
Light Sci Appl. 2023 Jul 12;12(1):172. doi: 10.1038/s41377-023-01204-4.
9
Fluorescence Microscopy: a statistics-optics perspective.荧光显微镜:统计学-光学视角
ArXiv. 2023 Oct 17:arXiv:2304.01456v3.
10
Nondestructive inspection of surface nanostructuring using label-free optical super-resolution imaging.使用无标记的光学超分辨率成像技术对表面纳米结构进行无损检测。
Sci Rep. 2023 Apr 12;13(1):6008. doi: 10.1038/s41598-023-32735-w.
Opt Lett. 2016 May 1;41(9):2109-12. doi: 10.1364/OL.41.002109.
4
Correlating confocal microscopy and atomic force indentation reveals metastatic cancer cells stiffen during invasion into collagen I matrices.共聚焦显微镜检查与原子力压痕技术的关联研究表明,转移性癌细胞在侵入I型胶原基质过程中会变硬。
Sci Rep. 2016 Jan 27;6:19686. doi: 10.1038/srep19686.
5
Super-resolution spinning-disk confocal microscopy using optical photon reassignment.使用光学光子重新分配的超分辨率旋转盘共聚焦显微镜。
Opt Express. 2015 Jun 1;23(11):15003-11. doi: 10.1364/OE.23.015003.
6
Two-photon instant structured illumination microscopy improves the depth penetration of super-resolution imaging in thick scattering samples.双光子即时结构照明显微镜提高了超分辨率成像在厚散射样品中的深度穿透能力。
Optica. 2014 Sep 20;1(3):181-191. doi: 10.1364/OPTICA.1.000181.
7
Two-photon excitation improves multifocal structured illumination microscopy in thick scattering tissue.双光子激发提高了厚散射组织中的多焦点结构照明显微镜技术。
Proc Natl Acad Sci U S A. 2014 Apr 8;111(14):5254-9. doi: 10.1073/pnas.1314447111. Epub 2014 Mar 24.
8
Resolution doubling in fluorescence microscopy with confocal spinning-disk image scanning microscopy.荧光显微镜中的分辨率提高两倍,采用共聚焦旋转盘图像扫描显微镜。
Proc Natl Acad Sci U S A. 2013 Dec 24;110(52):21000-5. doi: 10.1073/pnas.1315858110. Epub 2013 Dec 9.
9
Advances in multiphoton microscopy technology.多光子显微镜技术的进展。
Nat Photonics. 2013 Feb 1;7(2):93-101. doi: 10.1038/nphoton.2012.361.
10
Re-scan confocal microscopy: scanning twice for better resolution.重新扫描共聚焦显微镜:扫描两次以获得更高分辨率。
Biomed Opt Express. 2013 Oct 25;4(11):2644-56. doi: 10.1364/BOE.4.002644. eCollection 2013.