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Free-standing kinked nanowire transistor probes for targeted intracellular recording in three dimensions

Recording intracellular bioelectrical signals is central to understanding the fundamental behaviour of cells and cell-networks in, for example, neural and cardiac systems(1–4). The standard tool for intracellular recording, the patch-clamp micropipette(5) is widely applied, yet remains limited in te...

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Autores principales: Qing, Quan, Jiang, Zhe, Xu, Lin, Gao, Ruixuan, Mai, Liqiang, Lieber, Charles M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946362/
https://www.ncbi.nlm.nih.gov/pubmed/24336402
http://dx.doi.org/10.1038/nnano.2013.273
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author Qing, Quan
Jiang, Zhe
Xu, Lin
Gao, Ruixuan
Mai, Liqiang
Lieber, Charles M.
author_facet Qing, Quan
Jiang, Zhe
Xu, Lin
Gao, Ruixuan
Mai, Liqiang
Lieber, Charles M.
author_sort Qing, Quan
collection PubMed
description Recording intracellular bioelectrical signals is central to understanding the fundamental behaviour of cells and cell-networks in, for example, neural and cardiac systems(1–4). The standard tool for intracellular recording, the patch-clamp micropipette(5) is widely applied, yet remains limited in terms of reducing the tip size, the ability to reuse the pipette(5), and ion exchange with the cytoplasm(6). Recent efforts have been directed towards developing new chip-based tools(1–4,7–13), including micro-to-nanoscale metal pillars(7–9), transistor-based kinked nanowire(10,11) and nanotube devices(12,13). These nanoscale tools are interesting with respect to chip-based multiplexing, but, to date, preclude targeted recording from specific cell regions and/or subcellular structures. Here we overcome this limitation in a general manner by fabricating free-standing probes where a kinked silicon nanowire with encoded field-effect transistor detector serves as the tip end. These probes can be manipulated in three dimensions (3D) within a standard microscope to target specific cells/cell regions, and record stable full-amplitude intracellular action potentials from different targeted cells without the need to clean or change the tip. Simultaneous measurements from the same cell made with free-standing nanowire and patch-clamp probes show that the same action potential amplitude and temporal properties are recorded without corrections to the raw nanowire signal. In addition, we demonstrate real-time monitoring of changes in the action potential as different ion-channel blockers are applied to cells, and multiplexed recording from cells by independent manipulation of two free-standing nanowire probes.
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spelling pubmed-39463622014-08-01 Free-standing kinked nanowire transistor probes for targeted intracellular recording in three dimensions Qing, Quan Jiang, Zhe Xu, Lin Gao, Ruixuan Mai, Liqiang Lieber, Charles M. Nat Nanotechnol Article Recording intracellular bioelectrical signals is central to understanding the fundamental behaviour of cells and cell-networks in, for example, neural and cardiac systems(1–4). The standard tool for intracellular recording, the patch-clamp micropipette(5) is widely applied, yet remains limited in terms of reducing the tip size, the ability to reuse the pipette(5), and ion exchange with the cytoplasm(6). Recent efforts have been directed towards developing new chip-based tools(1–4,7–13), including micro-to-nanoscale metal pillars(7–9), transistor-based kinked nanowire(10,11) and nanotube devices(12,13). These nanoscale tools are interesting with respect to chip-based multiplexing, but, to date, preclude targeted recording from specific cell regions and/or subcellular structures. Here we overcome this limitation in a general manner by fabricating free-standing probes where a kinked silicon nanowire with encoded field-effect transistor detector serves as the tip end. These probes can be manipulated in three dimensions (3D) within a standard microscope to target specific cells/cell regions, and record stable full-amplitude intracellular action potentials from different targeted cells without the need to clean or change the tip. Simultaneous measurements from the same cell made with free-standing nanowire and patch-clamp probes show that the same action potential amplitude and temporal properties are recorded without corrections to the raw nanowire signal. In addition, we demonstrate real-time monitoring of changes in the action potential as different ion-channel blockers are applied to cells, and multiplexed recording from cells by independent manipulation of two free-standing nanowire probes. 2013-12-15 2014-02 /pmc/articles/PMC3946362/ /pubmed/24336402 http://dx.doi.org/10.1038/nnano.2013.273 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Qing, Quan
Jiang, Zhe
Xu, Lin
Gao, Ruixuan
Mai, Liqiang
Lieber, Charles M.
Free-standing kinked nanowire transistor probes for targeted intracellular recording in three dimensions
title Free-standing kinked nanowire transistor probes for targeted intracellular recording in three dimensions
title_full Free-standing kinked nanowire transistor probes for targeted intracellular recording in three dimensions
title_fullStr Free-standing kinked nanowire transistor probes for targeted intracellular recording in three dimensions
title_full_unstemmed Free-standing kinked nanowire transistor probes for targeted intracellular recording in three dimensions
title_short Free-standing kinked nanowire transistor probes for targeted intracellular recording in three dimensions
title_sort free-standing kinked nanowire transistor probes for targeted intracellular recording in three dimensions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946362/
https://www.ncbi.nlm.nih.gov/pubmed/24336402
http://dx.doi.org/10.1038/nnano.2013.273
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