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Lasers in Live Cell Microscopy

Due to their unique properties—coherent radiation, diffraction limited focusing, low spectral bandwidth and in many cases short light pulses—lasers play an increasing role in live cell microscopy. Lasers are indispensable tools in 3D microscopy, e.g., confocal, light sheet or total internal reflecti...

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Detalles Bibliográficos
Autor principal: Schneckenburger, Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102032/
https://www.ncbi.nlm.nih.gov/pubmed/35563406
http://dx.doi.org/10.3390/ijms23095015
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author Schneckenburger, Herbert
author_facet Schneckenburger, Herbert
author_sort Schneckenburger, Herbert
collection PubMed
description Due to their unique properties—coherent radiation, diffraction limited focusing, low spectral bandwidth and in many cases short light pulses—lasers play an increasing role in live cell microscopy. Lasers are indispensable tools in 3D microscopy, e.g., confocal, light sheet or total internal reflection microscopy, as well as in super-resolution microscopy using wide-field or confocal methods. Further techniques, e.g., spectral imaging or fluorescence lifetime imaging (FLIM) often depend on the well-defined spectral or temporal properties of lasers. Furthermore, laser microbeams are used increasingly for optical tweezers or micromanipulation of cells. Three exemplary laser applications in live cell biology are outlined. They include fluorescence diagnosis, in particular in combination with Förster Resonance Energy Transfer (FRET), photodynamic therapy as well as laser-assisted optoporation, and demonstrate the potential of lasers in cell biology and—more generally—in biomedicine.
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spelling pubmed-91020322022-05-14 Lasers in Live Cell Microscopy Schneckenburger, Herbert Int J Mol Sci Review Due to their unique properties—coherent radiation, diffraction limited focusing, low spectral bandwidth and in many cases short light pulses—lasers play an increasing role in live cell microscopy. Lasers are indispensable tools in 3D microscopy, e.g., confocal, light sheet or total internal reflection microscopy, as well as in super-resolution microscopy using wide-field or confocal methods. Further techniques, e.g., spectral imaging or fluorescence lifetime imaging (FLIM) often depend on the well-defined spectral or temporal properties of lasers. Furthermore, laser microbeams are used increasingly for optical tweezers or micromanipulation of cells. Three exemplary laser applications in live cell biology are outlined. They include fluorescence diagnosis, in particular in combination with Förster Resonance Energy Transfer (FRET), photodynamic therapy as well as laser-assisted optoporation, and demonstrate the potential of lasers in cell biology and—more generally—in biomedicine. MDPI 2022-04-30 /pmc/articles/PMC9102032/ /pubmed/35563406 http://dx.doi.org/10.3390/ijms23095015 Text en © 2022 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Schneckenburger, Herbert
Lasers in Live Cell Microscopy
title Lasers in Live Cell Microscopy
title_full Lasers in Live Cell Microscopy
title_fullStr Lasers in Live Cell Microscopy
title_full_unstemmed Lasers in Live Cell Microscopy
title_short Lasers in Live Cell Microscopy
title_sort lasers in live cell microscopy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102032/
https://www.ncbi.nlm.nih.gov/pubmed/35563406
http://dx.doi.org/10.3390/ijms23095015
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