Dynamics of intracellular processes in live-cell systems unveiled by fluorescence correlation microscopy

Fluorescence fluctuation-based methods are non-invasive microscopy tools especially suited for the study of dynamical aspects of biological processes. These methods examine spontaneous intensity fluctuations produced by fluorescent molecules moving through the small, femtoliter-sized observation vol...

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Autores principales: González Bardeci, N., Angiolini, J.F., De Rossi, M.C., Bruno, L., Levi, V.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_15216543_v69_n1_p8_GonzalezBardeci
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spelling todo:paper_15216543_v69_n1_p8_GonzalezBardeci2023-10-03T16:20:39Z Dynamics of intracellular processes in live-cell systems unveiled by fluorescence correlation microscopy González Bardeci, N. Angiolini, J.F. De Rossi, M.C. Bruno, L. Levi, V. autocorrelation cross-correlation diffusion fluorescence correlation spectroscopy fluorescence microscopy intracellular dynamics cell nucleus confocal microscopy cytology fluctuations technique fluorescence correlation microscopy fluorescence cross correlation spectroscopy fluorescence microscopy molecule nonhuman practice guideline quantitative analysis Review cells cytoplasm fluorescence molecular imaging procedures transport at the cellular level ultrastructure Biological Transport Cells Cytoplasm Fluorescence Microscopy, Fluorescence Molecular Imaging Fluorescence fluctuation-based methods are non-invasive microscopy tools especially suited for the study of dynamical aspects of biological processes. These methods examine spontaneous intensity fluctuations produced by fluorescent molecules moving through the small, femtoliter-sized observation volume defined in confocal and multiphoton microscopes. The quantitative analysis of the intensity trace provides information on the processes producing the fluctuations that include diffusion, binding interactions, chemical reactions and photophysical phenomena. In this review, we present the basic principles of the most widespread fluctuation-based methods, discuss their implementation in standard confocal microscopes and briefly revise some examples of their applications to address relevant questions in living cells. The ultimate goal of these methods in the Cell Biology field is to observe biomolecules as they move, interact with targets and perform their biological action in the natural context. © 2016 IUBMB Life, 69(1):8–15, 2017. © 2016 International Union of Biochemistry and Molecular Biology Fil:Bruno, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Levi, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_15216543_v69_n1_p8_GonzalezBardeci
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic autocorrelation
cross-correlation
diffusion
fluorescence correlation spectroscopy
fluorescence microscopy
intracellular dynamics
cell nucleus
confocal microscopy
cytology
fluctuations technique
fluorescence correlation microscopy
fluorescence cross correlation spectroscopy
fluorescence microscopy
molecule
nonhuman
practice guideline
quantitative analysis
Review
cells
cytoplasm
fluorescence
molecular imaging
procedures
transport at the cellular level
ultrastructure
Biological Transport
Cells
Cytoplasm
Fluorescence
Microscopy, Fluorescence
Molecular Imaging
spellingShingle autocorrelation
cross-correlation
diffusion
fluorescence correlation spectroscopy
fluorescence microscopy
intracellular dynamics
cell nucleus
confocal microscopy
cytology
fluctuations technique
fluorescence correlation microscopy
fluorescence cross correlation spectroscopy
fluorescence microscopy
molecule
nonhuman
practice guideline
quantitative analysis
Review
cells
cytoplasm
fluorescence
molecular imaging
procedures
transport at the cellular level
ultrastructure
Biological Transport
Cells
Cytoplasm
Fluorescence
Microscopy, Fluorescence
Molecular Imaging
González Bardeci, N.
Angiolini, J.F.
De Rossi, M.C.
Bruno, L.
Levi, V.
Dynamics of intracellular processes in live-cell systems unveiled by fluorescence correlation microscopy
topic_facet autocorrelation
cross-correlation
diffusion
fluorescence correlation spectroscopy
fluorescence microscopy
intracellular dynamics
cell nucleus
confocal microscopy
cytology
fluctuations technique
fluorescence correlation microscopy
fluorescence cross correlation spectroscopy
fluorescence microscopy
molecule
nonhuman
practice guideline
quantitative analysis
Review
cells
cytoplasm
fluorescence
molecular imaging
procedures
transport at the cellular level
ultrastructure
Biological Transport
Cells
Cytoplasm
Fluorescence
Microscopy, Fluorescence
Molecular Imaging
description Fluorescence fluctuation-based methods are non-invasive microscopy tools especially suited for the study of dynamical aspects of biological processes. These methods examine spontaneous intensity fluctuations produced by fluorescent molecules moving through the small, femtoliter-sized observation volume defined in confocal and multiphoton microscopes. The quantitative analysis of the intensity trace provides information on the processes producing the fluctuations that include diffusion, binding interactions, chemical reactions and photophysical phenomena. In this review, we present the basic principles of the most widespread fluctuation-based methods, discuss their implementation in standard confocal microscopes and briefly revise some examples of their applications to address relevant questions in living cells. The ultimate goal of these methods in the Cell Biology field is to observe biomolecules as they move, interact with targets and perform their biological action in the natural context. © 2016 IUBMB Life, 69(1):8–15, 2017. © 2016 International Union of Biochemistry and Molecular Biology
format JOUR
author González Bardeci, N.
Angiolini, J.F.
De Rossi, M.C.
Bruno, L.
Levi, V.
author_facet González Bardeci, N.
Angiolini, J.F.
De Rossi, M.C.
Bruno, L.
Levi, V.
author_sort González Bardeci, N.
title Dynamics of intracellular processes in live-cell systems unveiled by fluorescence correlation microscopy
title_short Dynamics of intracellular processes in live-cell systems unveiled by fluorescence correlation microscopy
title_full Dynamics of intracellular processes in live-cell systems unveiled by fluorescence correlation microscopy
title_fullStr Dynamics of intracellular processes in live-cell systems unveiled by fluorescence correlation microscopy
title_full_unstemmed Dynamics of intracellular processes in live-cell systems unveiled by fluorescence correlation microscopy
title_sort dynamics of intracellular processes in live-cell systems unveiled by fluorescence correlation microscopy
url http://hdl.handle.net/20.500.12110/paper_15216543_v69_n1_p8_GonzalezBardeci
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