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
Bredesen Center for Interdisciplinary Research, The University of Tennessee, Knoxville, USA.
Large Scale Structures Group, Neutron Scattering Division, Oak Ridge National Laboratory, Oak Ridge, USA.
MRS Bull. 2023;48(1):13-21. doi: 10.1557/s43577-022-00344-z. Epub 2022 Aug 29.
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 () 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.
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.
The online version contains supplementary material available at 10.1557/s43577-022-00344-z.
在生物学中,异突触可塑性在联想学习和记忆过程中维持突触输入的稳态,并引发突触强度的长期变化,这种变化会非特异性地调节不同类型的突触。在受生物启发的神经形态电路中,异突触可塑性可用于扩展双端仿生忆阻器的功能。在本文中,我们探讨了液滴界面双层水溶液的pH值变化如何在4.97 - 7.40的pH范围内调节脂质双层膜的忆阻响应。令人惊讶的是,我们没有找到确凿证据表明膜中形成短杆菌肽离子通道所需的电压阈值()存在pH依赖性偏移。然而,在时间依赖性脉冲电压实验中,我们确实观察到孔形成动力学随pH值有明显的调制。此外,在相同电压下,降低pH值会导致稳态电流升高,这是因为膜中导电肽离子通道数量增加。这是由于在pH 4.97时,短杆菌肽单体在膜中的分配增加,该pH值低于肽谷氨酸残基上羧基的pKa(约5.3 - 5.7),使得单体更疏水。在酸性条件下,这些残基上负电荷的中和增加了膜中肽单体的浓度,使膜中肽聚集体组装的平衡浓度向有利于形成更多更大、导电性越来越高的孔的方向移动。这也增加了孔形成和衰减的弛豫时间常数,并增强了器件开关特性的短期易化和抑制。全局且独立于短杆菌肽浓度和施加电压来调制这些阈值,将能够组装具有增强功能的神经形态计算电路。
我们描述了如何将pH用作一种调节性“中间神经元”,通过改变双层膜的结构和动力学特性来改变脂质双层中短杆菌肽离子通道的电压依赖性忆阻。能够独立于电压或离子通道浓度来控制孔传导的阈值水平,可在神经形态系统中实现额外的可编程性。在本文中,我们指出降低溶液pH值可降低膜结合离子通道的传导障碍,从而导致更高的电流,并以双脉冲易化的形式增强短期学习行为。利用诸如pH等环境变量来调整阈值,可提供额外的训练和学习算法,用于在脉冲神经网络中引发复杂功能。
在线版本包含可在10.1557/s43577 - 022 - 00344 - z获取的补充材料。