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Artifact-free and high-temporal-resolution in vivo opto-electrophysiology with microLED optoelectrodes

The combination of in vivo extracellular recording and genetic-engineering-assisted optical stimulation is a powerful tool for the study of neuronal circuits. Precise analysis of complex neural circuits requires high-density integration of multiple cellular-size light sources and recording electrode...

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Autores principales: Kim, Kanghwan, Vöröslakos, Mihály, Seymour, John P., Wise, Kensall D., Buzsáki, György, Yoon, Euisik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188816/
https://www.ncbi.nlm.nih.gov/pubmed/32345971
http://dx.doi.org/10.1038/s41467-020-15769-w
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author Kim, Kanghwan
Vöröslakos, Mihály
Seymour, John P.
Wise, Kensall D.
Buzsáki, György
Yoon, Euisik
author_facet Kim, Kanghwan
Vöröslakos, Mihály
Seymour, John P.
Wise, Kensall D.
Buzsáki, György
Yoon, Euisik
author_sort Kim, Kanghwan
collection PubMed
description The combination of in vivo extracellular recording and genetic-engineering-assisted optical stimulation is a powerful tool for the study of neuronal circuits. Precise analysis of complex neural circuits requires high-density integration of multiple cellular-size light sources and recording electrodes. However, high-density integration inevitably introduces stimulation artifact. We present minimal-stimulation-artifact (miniSTAR) μLED optoelectrodes that enable effective elimination of stimulation artifact. A multi-metal-layer structure with a shielding layer effectively suppresses capacitive coupling of stimulation signals. A heavily boron-doped silicon substrate silences the photovoltaic effect induced from LED illumination. With transient stimulation pulse shaping, we reduced stimulation artifact on miniSTAR μLED optoelectrodes to below 50 μV(pp), much smaller than a typical spike detection threshold, at optical stimulation of >50 mW mm(–2) irradiance. We demonstrated high-temporal resolution (<1 ms) opto-electrophysiology without any artifact-induced signal quality degradation during in vivo experiments. MiniSTAR μLED optoelectrodes will facilitate functional mapping of local circuits and discoveries in the brain.
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spelling pubmed-71888162020-05-01 Artifact-free and high-temporal-resolution in vivo opto-electrophysiology with microLED optoelectrodes Kim, Kanghwan Vöröslakos, Mihály Seymour, John P. Wise, Kensall D. Buzsáki, György Yoon, Euisik Nat Commun Article The combination of in vivo extracellular recording and genetic-engineering-assisted optical stimulation is a powerful tool for the study of neuronal circuits. Precise analysis of complex neural circuits requires high-density integration of multiple cellular-size light sources and recording electrodes. However, high-density integration inevitably introduces stimulation artifact. We present minimal-stimulation-artifact (miniSTAR) μLED optoelectrodes that enable effective elimination of stimulation artifact. A multi-metal-layer structure with a shielding layer effectively suppresses capacitive coupling of stimulation signals. A heavily boron-doped silicon substrate silences the photovoltaic effect induced from LED illumination. With transient stimulation pulse shaping, we reduced stimulation artifact on miniSTAR μLED optoelectrodes to below 50 μV(pp), much smaller than a typical spike detection threshold, at optical stimulation of >50 mW mm(–2) irradiance. We demonstrated high-temporal resolution (<1 ms) opto-electrophysiology without any artifact-induced signal quality degradation during in vivo experiments. MiniSTAR μLED optoelectrodes will facilitate functional mapping of local circuits and discoveries in the brain. Nature Publishing Group UK 2020-04-28 /pmc/articles/PMC7188816/ /pubmed/32345971 http://dx.doi.org/10.1038/s41467-020-15769-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kim, Kanghwan
Vöröslakos, Mihály
Seymour, John P.
Wise, Kensall D.
Buzsáki, György
Yoon, Euisik
Artifact-free and high-temporal-resolution in vivo opto-electrophysiology with microLED optoelectrodes
title Artifact-free and high-temporal-resolution in vivo opto-electrophysiology with microLED optoelectrodes
title_full Artifact-free and high-temporal-resolution in vivo opto-electrophysiology with microLED optoelectrodes
title_fullStr Artifact-free and high-temporal-resolution in vivo opto-electrophysiology with microLED optoelectrodes
title_full_unstemmed Artifact-free and high-temporal-resolution in vivo opto-electrophysiology with microLED optoelectrodes
title_short Artifact-free and high-temporal-resolution in vivo opto-electrophysiology with microLED optoelectrodes
title_sort artifact-free and high-temporal-resolution in vivo opto-electrophysiology with microled optoelectrodes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188816/
https://www.ncbi.nlm.nih.gov/pubmed/32345971
http://dx.doi.org/10.1038/s41467-020-15769-w
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