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More than double the fun with two-photon excitation microscopy
by
Fraser, Scott E.
, Schneider, Falk
, Luu, Peter
in
14
/ 14/69
/ 631/1647/245/2225
/ 631/1647/328/2057
/ Animals
/ Biomedical and Life Sciences
/ Cell differentiation
/ Cell migration
/ Fluorescence microscopy
/ Intravital Microscopy
/ Life Sciences
/ Microscopy
/ Microscopy, Fluorescence - methods
/ Microscopy, Fluorescence, Multiphoton - methods
/ Neurosciences
/ Photons
/ Review
/ Review Article
/ Spectroscopy
/ Spectrum Analysis
/ Trends
/ Wound healing
2024
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More than double the fun with two-photon excitation microscopy
by
Fraser, Scott E.
, Schneider, Falk
, Luu, Peter
in
14
/ 14/69
/ 631/1647/245/2225
/ 631/1647/328/2057
/ Animals
/ Biomedical and Life Sciences
/ Cell differentiation
/ Cell migration
/ Fluorescence microscopy
/ Intravital Microscopy
/ Life Sciences
/ Microscopy
/ Microscopy, Fluorescence - methods
/ Microscopy, Fluorescence, Multiphoton - methods
/ Neurosciences
/ Photons
/ Review
/ Review Article
/ Spectroscopy
/ Spectrum Analysis
/ Trends
/ Wound healing
2024
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Do you wish to request the book?
More than double the fun with two-photon excitation microscopy
by
Fraser, Scott E.
, Schneider, Falk
, Luu, Peter
in
14
/ 14/69
/ 631/1647/245/2225
/ 631/1647/328/2057
/ Animals
/ Biomedical and Life Sciences
/ Cell differentiation
/ Cell migration
/ Fluorescence microscopy
/ Intravital Microscopy
/ Life Sciences
/ Microscopy
/ Microscopy, Fluorescence - methods
/ Microscopy, Fluorescence, Multiphoton - methods
/ Neurosciences
/ Photons
/ Review
/ Review Article
/ Spectroscopy
/ Spectrum Analysis
/ Trends
/ Wound healing
2024
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More than double the fun with two-photon excitation microscopy
Journal Article
More than double the fun with two-photon excitation microscopy
2024
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Overview
For generations researchers have been observing the dynamic processes of life through the lens of a microscope. This has offered tremendous insights into biological phenomena that span multiple orders of time- and length-scales ranging from the pure magic of molecular reorganization at the membrane of immune cells, to cell migration and differentiation during development or wound healing. Standard fluorescence microscopy techniques offer glimpses at such processes in vitro, however, when applied in intact systems, they are challenged by reduced signal strengths and signal-to-noise ratios that result from deeper imaging. As a remedy, two-photon excitation (TPE) microscopy takes a special place, because it allows us to investigate processes in vivo, in their natural environment, even in a living animal. Here, we review the fundamental principles underlying TPE aimed at basic and advanced microscopy users interested in adopting TPE for intravital imaging. We focus on applications in neurobiology, present current trends towards faster, wider and deeper imaging, discuss the combination with photon counting technologies for metabolic imaging and spectroscopy, as well as highlight outstanding issues and drawbacks in development and application of these methodologies.
This review introduces the basic principle of fluorescence and two-photon excitation microscopy that is aimed at novice and advanced microscopists highlighting current techniques, trends, and practical guides for live imaging optimization.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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