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Heterosynaptic plasticity in biomembrane memristors controlled by pH

ABSTRACT: In biology, heterosynaptic plasticity maintains homeostasis in synaptic inputs during associative learning and memory, and initiates long-term changes in synaptic strengths that nonspecifically modulate different synapse types. In bioinspired neuromorphic circuits, heterosynaptic plasticit...

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Autores principales: McClintic, William T., Scott, Haden L., Moore, Nick, Farahat, Mustafa, Maxwell, Mikayla, Schuman, Catherine D., Bolmatov, Dima, Barrera, Francisco N., Katsaras, John, Collier, C. Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988737/
https://www.ncbi.nlm.nih.gov/pubmed/36908998
http://dx.doi.org/10.1557/s43577-022-00344-z
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author McClintic, William T.
Scott, Haden L.
Moore, Nick
Farahat, Mustafa
Maxwell, Mikayla
Schuman, Catherine D.
Bolmatov, Dima
Barrera, Francisco N.
Katsaras, John
Collier, C. Patrick
author_facet McClintic, William T.
Scott, Haden L.
Moore, Nick
Farahat, Mustafa
Maxwell, Mikayla
Schuman, Catherine D.
Bolmatov, Dima
Barrera, Francisco N.
Katsaras, John
Collier, C. Patrick
author_sort McClintic, William T.
collection PubMed
description ABSTRACT: In biology, heterosynaptic plasticity maintains homeostasis in synaptic inputs during associative learning and memory, and initiates long-term changes in synaptic strengths that nonspecifically modulate different synapse types. In bioinspired neuromorphic circuits, heterosynaptic plasticity may be used to extend the functionality of two-terminal, biomimetic memristors. In this article, we explore how changes in the pH of droplet interface bilayer aqueous solutions modulate the memristive responses of a lipid bilayer membrane in the pH range 4.97–7.40. Surprisingly, we did not find conclusive evidence for pH-dependent shifts in the voltage thresholds (V*) needed for alamethicin ion channel formation in the membrane. However, we did observe a clear modulation in the dynamics of pore formation with pH in time-dependent, pulsed voltage experiments. Moreover, at the same voltage, lowering the pH resulted in higher steady-state currents because of increased numbers of conductive peptide ion channels in the membrane. This was due to increased partitioning of alamethicin monomers into the membrane at pH 4.97, which is below the pKa (~5.3–5.7) of carboxylate groups on the glutamate residues of the peptide, making the monomers more hydrophobic. Neutralization of the negative charges on these residues, under acidic conditions, increased the concentration of peptide monomers in the membrane, shifting the equilibrium concentrations of peptide aggregate assemblies in the membrane to favor greater numbers of larger, increasingly more conductive pores. It also increased the relaxation time constants for pore formation and decay, and enhanced short-term facilitation and depression of the switching characteristics of the device. Modulating these thresholds globally and independently of alamethicin concentration and applied voltage will enable the assembly of neuromorphic computational circuitry with enhanced functionality. IMPACT STATEMENT: We describe how to use pH as a modulatory “interneuron” that changes the voltage-dependent memristance of alamethicin ion channels in lipid bilayers by changing the structure and dynamical properties of the bilayer. Having the ability to independently control the threshold levels for pore conduction from voltage or ion channel concentration enables additional levels of programmability in a neuromorphic system. In this article, we note that barriers to conduction from membrane-bound ion channels can be lowered by reducing solution pH, resulting in higher currents, and enhanced short-term learning behavior in the form of paired-pulse facilitation. Tuning threshold values with environmental variables, such as pH, provide additional training and learning algorithms that can be used to elicit complex functionality within spiking neural networks. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1557/s43577-022-00344-z.
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spelling pubmed-99887372023-03-08 Heterosynaptic plasticity in biomembrane memristors controlled by pH McClintic, William T. Scott, Haden L. Moore, Nick Farahat, Mustafa Maxwell, Mikayla Schuman, Catherine D. Bolmatov, Dima Barrera, Francisco N. Katsaras, John Collier, C. Patrick MRS Bull Impact Article ABSTRACT: In biology, heterosynaptic plasticity maintains homeostasis in synaptic inputs during associative learning and memory, and initiates long-term changes in synaptic strengths that nonspecifically modulate different synapse types. In bioinspired neuromorphic circuits, heterosynaptic plasticity may be used to extend the functionality of two-terminal, biomimetic memristors. In this article, we explore how changes in the pH of droplet interface bilayer aqueous solutions modulate the memristive responses of a lipid bilayer membrane in the pH range 4.97–7.40. Surprisingly, we did not find conclusive evidence for pH-dependent shifts in the voltage thresholds (V*) needed for alamethicin ion channel formation in the membrane. However, we did observe a clear modulation in the dynamics of pore formation with pH in time-dependent, pulsed voltage experiments. Moreover, at the same voltage, lowering the pH resulted in higher steady-state currents because of increased numbers of conductive peptide ion channels in the membrane. This was due to increased partitioning of alamethicin monomers into the membrane at pH 4.97, which is below the pKa (~5.3–5.7) of carboxylate groups on the glutamate residues of the peptide, making the monomers more hydrophobic. Neutralization of the negative charges on these residues, under acidic conditions, increased the concentration of peptide monomers in the membrane, shifting the equilibrium concentrations of peptide aggregate assemblies in the membrane to favor greater numbers of larger, increasingly more conductive pores. It also increased the relaxation time constants for pore formation and decay, and enhanced short-term facilitation and depression of the switching characteristics of the device. Modulating these thresholds globally and independently of alamethicin concentration and applied voltage will enable the assembly of neuromorphic computational circuitry with enhanced functionality. IMPACT STATEMENT: We describe how to use pH as a modulatory “interneuron” that changes the voltage-dependent memristance of alamethicin ion channels in lipid bilayers by changing the structure and dynamical properties of the bilayer. Having the ability to independently control the threshold levels for pore conduction from voltage or ion channel concentration enables additional levels of programmability in a neuromorphic system. In this article, we note that barriers to conduction from membrane-bound ion channels can be lowered by reducing solution pH, resulting in higher currents, and enhanced short-term learning behavior in the form of paired-pulse facilitation. Tuning threshold values with environmental variables, such as pH, provide additional training and learning algorithms that can be used to elicit complex functionality within spiking neural networks. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1557/s43577-022-00344-z. Springer International Publishing 2022-08-29 2023 /pmc/articles/PMC9988737/ /pubmed/36908998 http://dx.doi.org/10.1557/s43577-022-00344-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open accessThis 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Impact Article
McClintic, William T.
Scott, Haden L.
Moore, Nick
Farahat, Mustafa
Maxwell, Mikayla
Schuman, Catherine D.
Bolmatov, Dima
Barrera, Francisco N.
Katsaras, John
Collier, C. Patrick
Heterosynaptic plasticity in biomembrane memristors controlled by pH
title Heterosynaptic plasticity in biomembrane memristors controlled by pH
title_full Heterosynaptic plasticity in biomembrane memristors controlled by pH
title_fullStr Heterosynaptic plasticity in biomembrane memristors controlled by pH
title_full_unstemmed Heterosynaptic plasticity in biomembrane memristors controlled by pH
title_short Heterosynaptic plasticity in biomembrane memristors controlled by pH
title_sort heterosynaptic plasticity in biomembrane memristors controlled by ph
topic Impact Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988737/
https://www.ncbi.nlm.nih.gov/pubmed/36908998
http://dx.doi.org/10.1557/s43577-022-00344-z
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