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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Main Author: Graham C. R. Ellis-Davies
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-01-01
Series:Frontiers in Synaptic Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnsyn.2018.00048/full
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spelling 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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