Informational lesions: optical perturbation of spike timing and neural synchrony via microbial opsin gene fusions
Synchronous neural activity occurs throughout the brain in association with normal and pathological brain functions. Despite theoretical work exploring how such neural coordination might facilitate neural computation and be corrupted in disease states, it has proven difficult to test experimentally...
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2009-08-01
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doaj-98a936485810487dad89665657508ec52020-11-24T23:03:41ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992009-08-01210.3389/neuro.02.012.2009829Informational lesions: optical perturbation of spike timing and neural synchrony via microbial opsin gene fusionsXue Han0Xue Han1Xue Han2Xiaofeng Qian3Xiaofeng Qian4Patrick Stern5Amy Chuong6Edward S Boyden7Edward S Boyden8Edward S Boyden9Edward S Boyden10Massachusetts Institute of TechnologyMassachusetts Institute of TechnologyMassachusetts Institute of TechnologyMassachusetts Institute of TechnologyMassachusetts Institute of TechnologyMassachusetts Institute of TechnologyMassachusetts Institute of TechnologyMassachusetts Institute of TechnologyMassachusetts Institute of TechnologyMassachusetts Institute of TechnologyMassachusetts Institute of TechnologySynchronous neural activity occurs throughout the brain in association with normal and pathological brain functions. Despite theoretical work exploring how such neural coordination might facilitate neural computation and be corrupted in disease states, it has proven difficult to test experimentally the causal role of synchrony in such phenomena. Attempts to manipulate neural synchrony often alter other features of neural activity such as firing rate. Here we evaluate a single gene which encodes for the blue-light gated cation channel channelrhodopsin-2 and the yellow-light driven chloride pump halorhodopsin from N. pharaonis, linked by a ‘self-cleaving’ 2A peptide. This fusion enables proportional expression of both opsins, sensitizing neurons to being bi-directionally controlled with blue and yellow light, facilitating proportional optical spike insertion and deletion upon delivery of trains of precisely-timed blue and yellow light pulses. Such approaches may enable more detailed explorations of the causal role of specific features of the neural code.http://journal.frontiersin.org/Journal/10.3389/neuro.02.012.2009/fullsynchronyoptogeneticshalorhodopsinchannelrhodopsin-2fusion protein |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Xue Han Xue Han Xue Han Xiaofeng Qian Xiaofeng Qian Patrick Stern Amy Chuong Edward S Boyden Edward S Boyden Edward S Boyden Edward S Boyden |
spellingShingle |
Xue Han Xue Han Xue Han Xiaofeng Qian Xiaofeng Qian Patrick Stern Amy Chuong Edward S Boyden Edward S Boyden Edward S Boyden Edward S Boyden Informational lesions: optical perturbation of spike timing and neural synchrony via microbial opsin gene fusions Frontiers in Molecular Neuroscience synchrony optogenetics halorhodopsin channelrhodopsin-2 fusion protein |
author_facet |
Xue Han Xue Han Xue Han Xiaofeng Qian Xiaofeng Qian Patrick Stern Amy Chuong Edward S Boyden Edward S Boyden Edward S Boyden Edward S Boyden |
author_sort |
Xue Han |
title |
Informational lesions: optical perturbation of spike timing and neural synchrony via microbial opsin gene fusions |
title_short |
Informational lesions: optical perturbation of spike timing and neural synchrony via microbial opsin gene fusions |
title_full |
Informational lesions: optical perturbation of spike timing and neural synchrony via microbial opsin gene fusions |
title_fullStr |
Informational lesions: optical perturbation of spike timing and neural synchrony via microbial opsin gene fusions |
title_full_unstemmed |
Informational lesions: optical perturbation of spike timing and neural synchrony via microbial opsin gene fusions |
title_sort |
informational lesions: optical perturbation of spike timing and neural synchrony via microbial opsin gene fusions |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Molecular Neuroscience |
issn |
1662-5099 |
publishDate |
2009-08-01 |
description |
Synchronous neural activity occurs throughout the brain in association with normal and pathological brain functions. Despite theoretical work exploring how such neural coordination might facilitate neural computation and be corrupted in disease states, it has proven difficult to test experimentally the causal role of synchrony in such phenomena. Attempts to manipulate neural synchrony often alter other features of neural activity such as firing rate. Here we evaluate a single gene which encodes for the blue-light gated cation channel channelrhodopsin-2 and the yellow-light driven chloride pump halorhodopsin from N. pharaonis, linked by a ‘self-cleaving’ 2A peptide. This fusion enables proportional expression of both opsins, sensitizing neurons to being bi-directionally controlled with blue and yellow light, facilitating proportional optical spike insertion and deletion upon delivery of trains of precisely-timed blue and yellow light pulses. Such approaches may enable more detailed explorations of the causal role of specific features of the neural code. |
topic |
synchrony optogenetics halorhodopsin channelrhodopsin-2 fusion protein |
url |
http://journal.frontiersin.org/Journal/10.3389/neuro.02.012.2009/full |
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