An alternative to MINFLUX that enables nanometer resolution in a confocal microscope
- Autores
- Masullo, Luciano Andrés; Szalai, Alan Marcelo; Lopez, Lucía Fernanda; Pilo Pais, Mauricio; Acuna, Guillermo P.; Stefani, Fernando Daniel
- Año de publicación
- 2022
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Localization of single fluorescent emitters is key for physicochemical and biophysical measurements at the nanoscale and beyond ensemble averaging. Examples include single-molecule tracking and super-resolution imaging by single-molecule localization microscopy. Among the numerous localization methods available, MINFLUX outstands for achieving a ~10-fold improvement in resolution over wide-field camera-based approaches, reaching the molecular scale at moderate photon counts. Widespread application of MINFLUX and related methods has been hindered by the technical complexity of the setups. Here, we present RASTMIN, a single-molecule localization method based on raster scanning a light pattern comprising a minimum of intensity. RASTMIN delivers ~1–2 nm localization precision with usual fluorophores and is easily implementable on a standard confocal microscope with few modifications. We demonstrate the performance of RASTMIN in localization of single molecules and super-resolution imaging of DNA origami structures.
Fil: Masullo, Luciano Andrés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina
Fil: Szalai, Alan Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina
Fil: Lopez, Lucía Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina
Fil: Pilo Pais, Mauricio. Universite de Fribourg;
Fil: Acuna, Guillermo P.. Universite de Fribourg;
Fil: Stefani, Fernando Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina - Materia
-
NANOSCOPY
SINGLE MOLECULE
FLUORESCENCE
MOLECULAR RESOLUTION - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/203790
Ver los metadatos del registro completo
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An alternative to MINFLUX that enables nanometer resolution in a confocal microscopeMasullo, Luciano AndrésSzalai, Alan MarceloLopez, Lucía FernandaPilo Pais, MauricioAcuna, Guillermo P.Stefani, Fernando DanielNANOSCOPYSINGLE MOLECULEFLUORESCENCEMOLECULAR RESOLUTIONhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1https://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1https://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Localization of single fluorescent emitters is key for physicochemical and biophysical measurements at the nanoscale and beyond ensemble averaging. Examples include single-molecule tracking and super-resolution imaging by single-molecule localization microscopy. Among the numerous localization methods available, MINFLUX outstands for achieving a ~10-fold improvement in resolution over wide-field camera-based approaches, reaching the molecular scale at moderate photon counts. Widespread application of MINFLUX and related methods has been hindered by the technical complexity of the setups. Here, we present RASTMIN, a single-molecule localization method based on raster scanning a light pattern comprising a minimum of intensity. RASTMIN delivers ~1–2 nm localization precision with usual fluorophores and is easily implementable on a standard confocal microscope with few modifications. We demonstrate the performance of RASTMIN in localization of single molecules and super-resolution imaging of DNA origami structures.Fil: Masullo, Luciano Andrés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; ArgentinaFil: Szalai, Alan Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; ArgentinaFil: Lopez, Lucía Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; ArgentinaFil: Pilo Pais, Mauricio. Universite de Fribourg;Fil: Acuna, Guillermo P.. Universite de Fribourg;Fil: Stefani, Fernando Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; ArgentinaSpringer2022-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/203790Masullo, Luciano Andrés; Szalai, Alan Marcelo; Lopez, Lucía Fernanda; Pilo Pais, Mauricio; Acuna, Guillermo P.; et al.; An alternative to MINFLUX that enables nanometer resolution in a confocal microscope; Springer; Light: Science and Applications; 11; 1; 12-2022; 1-92047-7538CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1038/s41377-022-00896-4info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-17T11:14:41Zoai:ri.conicet.gov.ar:11336/203790instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-17 11:14:41.695CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
An alternative to MINFLUX that enables nanometer resolution in a confocal microscope |
title |
An alternative to MINFLUX that enables nanometer resolution in a confocal microscope |
spellingShingle |
An alternative to MINFLUX that enables nanometer resolution in a confocal microscope Masullo, Luciano Andrés NANOSCOPY SINGLE MOLECULE FLUORESCENCE MOLECULAR RESOLUTION |
title_short |
An alternative to MINFLUX that enables nanometer resolution in a confocal microscope |
title_full |
An alternative to MINFLUX that enables nanometer resolution in a confocal microscope |
title_fullStr |
An alternative to MINFLUX that enables nanometer resolution in a confocal microscope |
title_full_unstemmed |
An alternative to MINFLUX that enables nanometer resolution in a confocal microscope |
title_sort |
An alternative to MINFLUX that enables nanometer resolution in a confocal microscope |
dc.creator.none.fl_str_mv |
Masullo, Luciano Andrés Szalai, Alan Marcelo Lopez, Lucía Fernanda Pilo Pais, Mauricio Acuna, Guillermo P. Stefani, Fernando Daniel |
author |
Masullo, Luciano Andrés |
author_facet |
Masullo, Luciano Andrés Szalai, Alan Marcelo Lopez, Lucía Fernanda Pilo Pais, Mauricio Acuna, Guillermo P. Stefani, Fernando Daniel |
author_role |
author |
author2 |
Szalai, Alan Marcelo Lopez, Lucía Fernanda Pilo Pais, Mauricio Acuna, Guillermo P. Stefani, Fernando Daniel |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
NANOSCOPY SINGLE MOLECULE FLUORESCENCE MOLECULAR RESOLUTION |
topic |
NANOSCOPY SINGLE MOLECULE FLUORESCENCE MOLECULAR RESOLUTION |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Localization of single fluorescent emitters is key for physicochemical and biophysical measurements at the nanoscale and beyond ensemble averaging. Examples include single-molecule tracking and super-resolution imaging by single-molecule localization microscopy. Among the numerous localization methods available, MINFLUX outstands for achieving a ~10-fold improvement in resolution over wide-field camera-based approaches, reaching the molecular scale at moderate photon counts. Widespread application of MINFLUX and related methods has been hindered by the technical complexity of the setups. Here, we present RASTMIN, a single-molecule localization method based on raster scanning a light pattern comprising a minimum of intensity. RASTMIN delivers ~1–2 nm localization precision with usual fluorophores and is easily implementable on a standard confocal microscope with few modifications. We demonstrate the performance of RASTMIN in localization of single molecules and super-resolution imaging of DNA origami structures. Fil: Masullo, Luciano Andrés. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: Szalai, Alan Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: Lopez, Lucía Fernanda. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina Fil: Pilo Pais, Mauricio. Universite de Fribourg; Fil: Acuna, Guillermo P.. Universite de Fribourg; Fil: Stefani, Fernando Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Bionanociencias "Elizabeth Jares Erijman"; Argentina |
description |
Localization of single fluorescent emitters is key for physicochemical and biophysical measurements at the nanoscale and beyond ensemble averaging. Examples include single-molecule tracking and super-resolution imaging by single-molecule localization microscopy. Among the numerous localization methods available, MINFLUX outstands for achieving a ~10-fold improvement in resolution over wide-field camera-based approaches, reaching the molecular scale at moderate photon counts. Widespread application of MINFLUX and related methods has been hindered by the technical complexity of the setups. Here, we present RASTMIN, a single-molecule localization method based on raster scanning a light pattern comprising a minimum of intensity. RASTMIN delivers ~1–2 nm localization precision with usual fluorophores and is easily implementable on a standard confocal microscope with few modifications. We demonstrate the performance of RASTMIN in localization of single molecules and super-resolution imaging of DNA origami structures. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-12 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/203790 Masullo, Luciano Andrés; Szalai, Alan Marcelo; Lopez, Lucía Fernanda; Pilo Pais, Mauricio; Acuna, Guillermo P.; et al.; An alternative to MINFLUX that enables nanometer resolution in a confocal microscope; Springer; Light: Science and Applications; 11; 1; 12-2022; 1-9 2047-7538 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/203790 |
identifier_str_mv |
Masullo, Luciano Andrés; Szalai, Alan Marcelo; Lopez, Lucía Fernanda; Pilo Pais, Mauricio; Acuna, Guillermo P.; et al.; An alternative to MINFLUX that enables nanometer resolution in a confocal microscope; Springer; Light: Science and Applications; 11; 1; 12-2022; 1-9 2047-7538 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41377-022-00896-4 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Springer |
publisher.none.fl_str_mv |
Springer |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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13.001348 |