Nitroso-Caged Rhodamine: A Superior Green Light-Activatable Fluorophore for Single-Molecule Localization Super-Resolution Imaging
The evolution of super-resolution imaging techniques, especially single-molecule localization microscopy, demands the engineering of switchable fluorophores with labeling functionality. Yet, the switching of these fluorophores depends on the exterior conditions of UV light and enhancing buffers, whi...
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Veröffentlicht in: | Analytical chemistry (Washington) 2021-06, Vol.93 (22), p.7833-7842 |
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creator | Zheng, Ying Ye, Zhiwei Liu, Zengjin Yang, Wei Zhang, Xinfu Yang, Youjun Xiao, Yi |
description | The evolution of super-resolution imaging techniques, especially single-molecule localization microscopy, demands the engineering of switchable fluorophores with labeling functionality. Yet, the switching of these fluorophores depends on the exterior conditions of UV light and enhancing buffers, which is bioincompatible for living-cell applications. Herein, to surpass these limitations, a nitroso-caging strategy is employed to cage rhodamines into leuco forms, which for the first time, is discovered to uncage highly bright zwitterions by green light. Further, clickable construction grants the specificity and versatility for labeling various components in living cells. The simultaneous photoactivation and excitation of these novel probes allow for single-laser super-resolution imaging without any harmful additives. Super-resolution imaging of microtubules in fixed cells or mitochondria and the distribution of glycans and H2B proteins in living cells are achieved at a molecular scale with robust integrity. We envision that our nitroso-caging probes would set a platform for the development of future visible-activatable probes. |
doi_str_mv | 10.1021/acs.analchem.1c00175 |
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Yet, the switching of these fluorophores depends on the exterior conditions of UV light and enhancing buffers, which is bioincompatible for living-cell applications. Herein, to surpass these limitations, a nitroso-caging strategy is employed to cage rhodamines into leuco forms, which for the first time, is discovered to uncage highly bright zwitterions by green light. Further, clickable construction grants the specificity and versatility for labeling various components in living cells. The simultaneous photoactivation and excitation of these novel probes allow for single-laser super-resolution imaging without any harmful additives. Super-resolution imaging of microtubules in fixed cells or mitochondria and the distribution of glycans and H2B proteins in living cells are achieved at a molecular scale with robust integrity. 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Super-resolution imaging of microtubules in fixed cells or mitochondria and the distribution of glycans and H2B proteins in living cells are achieved at a molecular scale with robust integrity. 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Ye, Zhiwei ; Liu, Zengjin ; Yang, Wei ; Zhang, Xinfu ; Yang, Youjun ; Xiao, Yi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a353t-5354c8d7740540cef3b2f4628b3a50bbd2ce8a856c0eb1e27ee7ccbb49740cb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Additives</topic><topic>Analytical chemistry</topic><topic>Cells (biology)</topic><topic>Chemical compounds</topic><topic>Chemistry</topic><topic>Fluorescence</topic><topic>Fluorophores</topic><topic>Image resolution</topic><topic>Imaging techniques</topic><topic>Labeling</topic><topic>Localization</topic><topic>Microtubules</topic><topic>Mitochondria</topic><topic>Photoactivation</topic><topic>Polysaccharides</topic><topic>Probes</topic><topic>Rhodamine</topic><topic>Ultraviolet radiation</topic><topic>Zwitterions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheng, Ying</creatorcontrib><creatorcontrib>Ye, Zhiwei</creatorcontrib><creatorcontrib>Liu, Zengjin</creatorcontrib><creatorcontrib>Yang, Wei</creatorcontrib><creatorcontrib>Zhang, Xinfu</creatorcontrib><creatorcontrib>Yang, Youjun</creatorcontrib><creatorcontrib>Xiao, Yi</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical chemistry (Washington)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheng, Ying</au><au>Ye, Zhiwei</au><au>Liu, Zengjin</au><au>Yang, Wei</au><au>Zhang, Xinfu</au><au>Yang, Youjun</au><au>Xiao, Yi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitroso-Caged Rhodamine: A Superior Green Light-Activatable Fluorophore for Single-Molecule Localization Super-Resolution Imaging</atitle><jtitle>Analytical chemistry (Washington)</jtitle><addtitle>Anal. Chem</addtitle><date>2021-06-08</date><risdate>2021</risdate><volume>93</volume><issue>22</issue><spage>7833</spage><epage>7842</epage><pages>7833-7842</pages><issn>0003-2700</issn><eissn>1520-6882</eissn><abstract>The evolution of super-resolution imaging techniques, especially single-molecule localization microscopy, demands the engineering of switchable fluorophores with labeling functionality. Yet, the switching of these fluorophores depends on the exterior conditions of UV light and enhancing buffers, which is bioincompatible for living-cell applications. Herein, to surpass these limitations, a nitroso-caging strategy is employed to cage rhodamines into leuco forms, which for the first time, is discovered to uncage highly bright zwitterions by green light. Further, clickable construction grants the specificity and versatility for labeling various components in living cells. The simultaneous photoactivation and excitation of these novel probes allow for single-laser super-resolution imaging without any harmful additives. Super-resolution imaging of microtubules in fixed cells or mitochondria and the distribution of glycans and H2B proteins in living cells are achieved at a molecular scale with robust integrity. We envision that our nitroso-caging probes would set a platform for the development of future visible-activatable probes.</abstract><cop>Washington</cop><pub>American Chemical Society</pub><doi>10.1021/acs.analchem.1c00175</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-7085-6048</orcidid><orcidid>https://orcid.org/0000-0002-4055-3676</orcidid><orcidid>https://orcid.org/0000-0001-5544-1522</orcidid></addata></record> |
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subjects | Additives Analytical chemistry Cells (biology) Chemical compounds Chemistry Fluorescence Fluorophores Image resolution Imaging techniques Labeling Localization Microtubules Mitochondria Photoactivation Polysaccharides Probes Rhodamine Ultraviolet radiation Zwitterions |
title | Nitroso-Caged Rhodamine: A Superior Green Light-Activatable Fluorophore for Single-Molecule Localization Super-Resolution Imaging |
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