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- W2181874467 abstract "tons should produce glutamate in proportion to the Functional mapping of neurotransmitter receptors resquare of the light intensity and do so primarily at the quires rapid and localized application of transmitter. focal plane. We tested this strategy in hippocampal pyThe usefulness of caged glutamate for this purpose ramidal neurons by comparing the performance of a has been limited, because photolysis by unfocused novel double-caged glutamate to that of a single-caged light above and below the target cell limits depth resoglutamate, and we report that this approach substanlution. This problem is eliminated by using a doubletially improves depth resolution. caged glutamate that requires absorption of two photons for conversion to active glutamate, resulting in a substantial improvement in spatial resolution over Results conventional caged glutamate. This method was used to map the distribution of glutamate receptors on hipTheory and Predictions pocampal pyramidal neurons. A higher density of As UV light is focused on a specimen, it passes through AMPA receptors was found on distal apical dendrites a double cone-shaped volume in which glutamate can than on basal or primary apical dendrites, suggesting be produced (Figure1B). In ourmicroscope, light passes that synaptic efficacy is locally heterogeneous. Such through a multimode optical fiber that transmits an ap“chemical two-photon uncaging” offers a simple, genproximately Gaussian light beamthat overfills (total poseral, and economical strategy for spatially localized sible angle of 648) the back aperture of a water-immerphotolysis of caged compounds. sion objective (numerical aperture of 0.7). The objective" @default.
- W2181874467 created "2016-06-24" @default.
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- W2181874467 date "1997-01-01" @default.
- W2181874467 modified "2023-09-27" @default.
- W2181874467 title "Chemical Two-Photon Uncaging: Neurotechnique a Novel Approach to Mapping Glutamate Receptors" @default.
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