resPAINT: Accelerating Volumetric Super‐Resolution Localisation Microscopy by Active Control of Probe Emission
Points for accumulation in nanoscale topography (PAINT) allows practically unlimited measurements in localisation microscopy but is limited by background fluorescence at high probe concentrations, especially in volumetric imaging. We present reservoir‐PAINT (resPAINT), which combines PAINT and activ...
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Veröffentlicht in: | Angewandte Chemie 2022-10, Vol.134 (42), p.e202206919-n/a |
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creator | Sanders, Edward W. Carr, Alexander R. Bruggeman, Ezra Körbel, Markus Benaissa, Sarah I. Donat, Robert F. Santos, Ana M. McColl, James O'Holleran, Kevin Klenerman, David Davis, Simon J. Lee, Steven F. Ponjavic, Aleks |
description | Points for accumulation in nanoscale topography (PAINT) allows practically unlimited measurements in localisation microscopy but is limited by background fluorescence at high probe concentrations, especially in volumetric imaging. We present reservoir‐PAINT (resPAINT), which combines PAINT and active control of probe photophysics. In resPAINT, an activatable probe “reservoir” accumulates on target, enabling a 50‐fold increase in localisation rate versus conventional PAINT, without compromising contrast. By combining resPAINT with large depth‐of‐field microscopy, we demonstrate super‐resolution imaging of entire cell surfaces. We generalise the approach by implementing various switching strategies and 3D imaging techniques. Finally, we use resPAINT with a Fab to image membrane proteins, extending the operating regime of PAINT to include a wider range of biological interactions.
A new super‐resolution technique for localisation microscopy, which combines active control of probe photophysics with stochastic binding is reported. resPAINT yields an up to 50‐fold improvement in localisation rate vs. PAINT without compromising contrast and is fully compatible with large depth of field imaging techniques. This opens the door to larger scale 3D localisation microscopy as imaging that normally takes days can now be completed in hours. |
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A new super‐resolution technique for localisation microscopy, which combines active control of probe photophysics with stochastic binding is reported. resPAINT yields an up to 50‐fold improvement in localisation rate vs. PAINT without compromising contrast and is fully compatible with large depth of field imaging techniques. This opens the door to larger scale 3D localisation microscopy as imaging that normally takes days can now be completed in hours.</description><identifier>ISSN: 0044-8249</identifier><identifier>EISSN: 1521-3757</identifier><identifier>DOI: 10.1002/ange.202206919</identifier><identifier>PMID: 38505515</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Active control ; Biophysics ; Chemistry ; Emissions control ; Fluorescence ; Forschungsartikel ; Imaging techniques ; Localisation Microscopy ; Localization ; Membrane proteins ; Microscopy ; PAINT ; Reservoirs ; Single-Molecule Imaging ; Super-Resolution Microscopy</subject><ispartof>Angewandte Chemie, 2022-10, Vol.134 (42), p.e202206919-n/a</ispartof><rights>2022 The Authors. Angewandte Chemie published by Wiley-VCH GmbH</rights><rights>2022 The Authors. Angewandte Chemie published by Wiley-VCH GmbH.</rights><rights>2022. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3149-3dc74e46b22261c12c46ffc61be630c8f0fd385abde99f2a20baec2b97ccbac3</citedby><cites>FETCH-LOGICAL-c3149-3dc74e46b22261c12c46ffc61be630c8f0fd385abde99f2a20baec2b97ccbac3</cites><orcidid>0000-0002-7561-1127 ; 0000-0002-8972-7702</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fange.202206919$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fange.202206919$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38505515$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sanders, Edward W.</creatorcontrib><creatorcontrib>Carr, Alexander R.</creatorcontrib><creatorcontrib>Bruggeman, Ezra</creatorcontrib><creatorcontrib>Körbel, Markus</creatorcontrib><creatorcontrib>Benaissa, Sarah I.</creatorcontrib><creatorcontrib>Donat, Robert F.</creatorcontrib><creatorcontrib>Santos, Ana M.</creatorcontrib><creatorcontrib>McColl, James</creatorcontrib><creatorcontrib>O'Holleran, Kevin</creatorcontrib><creatorcontrib>Klenerman, David</creatorcontrib><creatorcontrib>Davis, Simon J.</creatorcontrib><creatorcontrib>Lee, Steven F.</creatorcontrib><creatorcontrib>Ponjavic, Aleks</creatorcontrib><title>resPAINT: Accelerating Volumetric Super‐Resolution Localisation Microscopy by Active Control of Probe Emission</title><title>Angewandte Chemie</title><addtitle>Angew Chem Weinheim Bergstr Ger</addtitle><description>Points for accumulation in nanoscale topography (PAINT) allows practically unlimited measurements in localisation microscopy but is limited by background fluorescence at high probe concentrations, especially in volumetric imaging. We present reservoir‐PAINT (resPAINT), which combines PAINT and active control of probe photophysics. In resPAINT, an activatable probe “reservoir” accumulates on target, enabling a 50‐fold increase in localisation rate versus conventional PAINT, without compromising contrast. By combining resPAINT with large depth‐of‐field microscopy, we demonstrate super‐resolution imaging of entire cell surfaces. We generalise the approach by implementing various switching strategies and 3D imaging techniques. Finally, we use resPAINT with a Fab to image membrane proteins, extending the operating regime of PAINT to include a wider range of biological interactions.
A new super‐resolution technique for localisation microscopy, which combines active control of probe photophysics with stochastic binding is reported. resPAINT yields an up to 50‐fold improvement in localisation rate vs. PAINT without compromising contrast and is fully compatible with large depth of field imaging techniques. This opens the door to larger scale 3D localisation microscopy as imaging that normally takes days can now be completed in hours.</description><subject>Active control</subject><subject>Biophysics</subject><subject>Chemistry</subject><subject>Emissions control</subject><subject>Fluorescence</subject><subject>Forschungsartikel</subject><subject>Imaging techniques</subject><subject>Localisation Microscopy</subject><subject>Localization</subject><subject>Membrane proteins</subject><subject>Microscopy</subject><subject>PAINT</subject><subject>Reservoirs</subject><subject>Single-Molecule Imaging</subject><subject>Super-Resolution Microscopy</subject><issn>0044-8249</issn><issn>1521-3757</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkctuEzEUhi0EoqGwZYlGYsNmwvGZi8dsUBSFUimUCiK2lsc5E1xNxlN7pii7PkKfkSfBISVcNqws258_nd8_Y885TDkAvtbdhqYIiFBKLh-wCS-Qp5koxEM2AcjztMJcnrAnIVwBQIlCPmYnWVVAUfBiwnpP4XJ2frF6k8yMoZa8Hmy3Sb64dtzS4K1JPo89-e-3d58oxMPBui5ZOqNbG_TPzQdrvAvG9buk3kXLYG8ombtu8K5NXJNceldTstjaECL-lD1qdBvo2f16ylbvFqv5-3T58ex8PlumJuO5TLO1ETnlZY2IJTccTV42jSl5TWUGpmqgWccUul6TlA1qhFqTwVoKY2ptslP29qDtx3pLa0NxHN2q3tut9jvltFV_33T2q9q4G8VB5mWZZdHw6t7g3fVIYVAxQfyhVnfkxqBQChRQiBwi-vIf9MqNvovxFArMsIKKi0hND9T-u4Kn5jgNB7UvU-3LVMcy44MXf2Y44r_ai4A8AN9sS7v_6NTs4mzxW_4DjUWvhA</recordid><startdate>20221017</startdate><enddate>20221017</enddate><creator>Sanders, Edward W.</creator><creator>Carr, Alexander R.</creator><creator>Bruggeman, Ezra</creator><creator>Körbel, Markus</creator><creator>Benaissa, Sarah I.</creator><creator>Donat, Robert F.</creator><creator>Santos, Ana M.</creator><creator>McColl, James</creator><creator>O'Holleran, Kevin</creator><creator>Klenerman, David</creator><creator>Davis, Simon J.</creator><creator>Lee, Steven F.</creator><creator>Ponjavic, Aleks</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7561-1127</orcidid><orcidid>https://orcid.org/0000-0002-8972-7702</orcidid></search><sort><creationdate>20221017</creationdate><title>resPAINT: Accelerating Volumetric Super‐Resolution Localisation Microscopy by Active Control of Probe Emission</title><author>Sanders, Edward W. ; Carr, Alexander R. ; Bruggeman, Ezra ; Körbel, Markus ; Benaissa, Sarah I. ; Donat, Robert F. ; Santos, Ana M. ; McColl, James ; O'Holleran, Kevin ; Klenerman, David ; Davis, Simon J. ; Lee, Steven F. ; Ponjavic, Aleks</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3149-3dc74e46b22261c12c46ffc61be630c8f0fd385abde99f2a20baec2b97ccbac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Active control</topic><topic>Biophysics</topic><topic>Chemistry</topic><topic>Emissions control</topic><topic>Fluorescence</topic><topic>Forschungsartikel</topic><topic>Imaging techniques</topic><topic>Localisation Microscopy</topic><topic>Localization</topic><topic>Membrane proteins</topic><topic>Microscopy</topic><topic>PAINT</topic><topic>Reservoirs</topic><topic>Single-Molecule Imaging</topic><topic>Super-Resolution Microscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sanders, Edward W.</creatorcontrib><creatorcontrib>Carr, Alexander R.</creatorcontrib><creatorcontrib>Bruggeman, Ezra</creatorcontrib><creatorcontrib>Körbel, Markus</creatorcontrib><creatorcontrib>Benaissa, Sarah I.</creatorcontrib><creatorcontrib>Donat, Robert F.</creatorcontrib><creatorcontrib>Santos, Ana M.</creatorcontrib><creatorcontrib>McColl, James</creatorcontrib><creatorcontrib>O'Holleran, Kevin</creatorcontrib><creatorcontrib>Klenerman, David</creatorcontrib><creatorcontrib>Davis, Simon J.</creatorcontrib><creatorcontrib>Lee, Steven F.</creatorcontrib><creatorcontrib>Ponjavic, Aleks</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Angewandte Chemie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sanders, Edward W.</au><au>Carr, Alexander R.</au><au>Bruggeman, Ezra</au><au>Körbel, Markus</au><au>Benaissa, Sarah I.</au><au>Donat, Robert F.</au><au>Santos, Ana M.</au><au>McColl, James</au><au>O'Holleran, Kevin</au><au>Klenerman, David</au><au>Davis, Simon J.</au><au>Lee, Steven F.</au><au>Ponjavic, Aleks</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>resPAINT: Accelerating Volumetric Super‐Resolution Localisation Microscopy by Active Control of Probe Emission</atitle><jtitle>Angewandte Chemie</jtitle><addtitle>Angew Chem Weinheim Bergstr Ger</addtitle><date>2022-10-17</date><risdate>2022</risdate><volume>134</volume><issue>42</issue><spage>e202206919</spage><epage>n/a</epage><pages>e202206919-n/a</pages><issn>0044-8249</issn><eissn>1521-3757</eissn><abstract>Points for accumulation in nanoscale topography (PAINT) allows practically unlimited measurements in localisation microscopy but is limited by background fluorescence at high probe concentrations, especially in volumetric imaging. We present reservoir‐PAINT (resPAINT), which combines PAINT and active control of probe photophysics. In resPAINT, an activatable probe “reservoir” accumulates on target, enabling a 50‐fold increase in localisation rate versus conventional PAINT, without compromising contrast. By combining resPAINT with large depth‐of‐field microscopy, we demonstrate super‐resolution imaging of entire cell surfaces. We generalise the approach by implementing various switching strategies and 3D imaging techniques. Finally, we use resPAINT with a Fab to image membrane proteins, extending the operating regime of PAINT to include a wider range of biological interactions.
A new super‐resolution technique for localisation microscopy, which combines active control of probe photophysics with stochastic binding is reported. resPAINT yields an up to 50‐fold improvement in localisation rate vs. PAINT without compromising contrast and is fully compatible with large depth of field imaging techniques. This opens the door to larger scale 3D localisation microscopy as imaging that normally takes days can now be completed in hours.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38505515</pmid><doi>10.1002/ange.202206919</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-7561-1127</orcidid><orcidid>https://orcid.org/0000-0002-8972-7702</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Active control Biophysics Chemistry Emissions control Fluorescence Forschungsartikel Imaging techniques Localisation Microscopy Localization Membrane proteins Microscopy PAINT Reservoirs Single-Molecule Imaging Super-Resolution Microscopy |
title | resPAINT: Accelerating Volumetric Super‐Resolution Localisation Microscopy by Active Control of Probe Emission |
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