Two-Photon Uncaging of Glutamate
Two-photon microscopy produces the excited singlet state of a chromophore with wavelengths approximately double that used for normal excitation. Two photons are absorbed almost simultaneously, via a virtual state, and this makes the excitation technique inherently non-linear. It requires ultra-fast...
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Online Access: | https://www.frontiersin.org/article/10.3389/fnsyn.2018.00048/full |
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doaj-94f9fc1b7a0849a3b196707a668a0af02020-11-24T21:10:27ZengFrontiers Media S.A.Frontiers in Synaptic Neuroscience1663-35632019-01-011010.3389/fnsyn.2018.00048434745Two-Photon Uncaging of GlutamateGraham C. R. Ellis-DaviesTwo-photon microscopy produces the excited singlet state of a chromophore with wavelengths approximately double that used for normal excitation. Two photons are absorbed almost simultaneously, via a virtual state, and this makes the excitation technique inherently non-linear. It requires ultra-fast lasers to deliver the high flux density needed to access intrinsically very short lived intermediates, and in combination with lenses of high numerical aperture, this confines axial excitation highly. Since the two-photon excitation volume is similar to a large spine head, the technique has been widely used to study glutamatergic transmission in brain slices. Here I describe the principles of two-photon uncaging of glutamate and provide a practical guide to its application.https://www.frontiersin.org/article/10.3389/fnsyn.2018.00048/fullGlu = glutamate2-photonuncagingquantaplasticitydendritic spikes |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Graham C. R. Ellis-Davies |
spellingShingle |
Graham C. R. Ellis-Davies Two-Photon Uncaging of Glutamate Frontiers in Synaptic Neuroscience Glu = glutamate 2-photon uncaging quanta plasticity dendritic spikes |
author_facet |
Graham C. R. Ellis-Davies |
author_sort |
Graham C. R. Ellis-Davies |
title |
Two-Photon Uncaging of Glutamate |
title_short |
Two-Photon Uncaging of Glutamate |
title_full |
Two-Photon Uncaging of Glutamate |
title_fullStr |
Two-Photon Uncaging of Glutamate |
title_full_unstemmed |
Two-Photon Uncaging of Glutamate |
title_sort |
two-photon uncaging of glutamate |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Synaptic Neuroscience |
issn |
1663-3563 |
publishDate |
2019-01-01 |
description |
Two-photon microscopy produces the excited singlet state of a chromophore with wavelengths approximately double that used for normal excitation. Two photons are absorbed almost simultaneously, via a virtual state, and this makes the excitation technique inherently non-linear. It requires ultra-fast lasers to deliver the high flux density needed to access intrinsically very short lived intermediates, and in combination with lenses of high numerical aperture, this confines axial excitation highly. Since the two-photon excitation volume is similar to a large spine head, the technique has been widely used to study glutamatergic transmission in brain slices. Here I describe the principles of two-photon uncaging of glutamate and provide a practical guide to its application. |
topic |
Glu = glutamate 2-photon uncaging quanta plasticity dendritic spikes |
url |
https://www.frontiersin.org/article/10.3389/fnsyn.2018.00048/full |
work_keys_str_mv |
AT grahamcrellisdavies twophotonuncagingofglutamate |
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