Abstract
Phospholipid bilayers can be described as capacitors whose capacitance per unit area (specific capacitance, Cm) is determined by their thickness and dielectric constant─independent of applied voltage. It is also widely assumed that the Cm of membranes can be treated as a “biological constant”. Recently, using droplet interface bilayers (DIBs), it was shown that zwitterionic phosphatidylcholine (PC) lipid bilayers can act as voltage-dependent, nonlinear memory capacitors, or memcapacitors. When exposed to an electrical “training” stimulation protocol, capacitive energy storage in lipid membranes was enhanced in the form of long-term potentiation (LTP), which enables biological learning and long-term memory. LTP was the result of membrane restructuring and the progressive asymmetric distribution of ions across the lipid bilayer during training, which is analogous, for example, to exponential capacitive energy harvesting from self-powered nanogenerators. Here, we describe how LTP could be produced from a membrane that is continuously pumped into a nonequilibrium steady state, altering its dielectric properties. During this time, the membrane undergoes static and dynamic changes that are fed back to the system’s potential energy, ultimately resulting in a membrane whose modified molecular structure supports long-term memory storage and LTP. We also show that LTP is very sensitive to different salts (KCl, NaCl, LiCl, and TmCl3), with LiCl and TmCl3 having the most profound effect in depressing LTP, relative to KCl. This effect is related to how the different cations interact with the bilayer zwitterionic PC lipid headgroups primarily through electric-field-induced changes to the statistically averaged orientations of water dipoles at the bilayer headgroup interface.
Original language | English |
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Pages (from-to) | 44533-44540 |
Number of pages | 8 |
Journal | ACS Applied Materials and Interfaces |
Volume | 15 |
Issue number | 37 |
DOIs | |
State | Published - Sep 20 2023 |
Funding
J.K. would like to thank Fyl Pincus (University of California Santa Barbara) for many fruitful discussions. H.L.S., J.K., and C.P.C. are supported through the Scientific User Facilities Division of the Department of Energy (DOE) Office of Science, sponsored by the Basic Energy Science (BES) Program, DOE Office of Science, under Contract No. DEAC05-00OR22725. D.B. and M.L. are supported through the National Science Foundation, Division of Molecular and Cellular Biosciences (MCB), under contract no. 2219289. Data collection and analysis were performed at the Center for Nanophase Materials Sciences, a US DOE Office of Science User Facility. SFG measurements and analysis by U.I.P. and B.D. were supported by the U.S. DOE, Office of Science, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division. This research used resources of the Oak Ridge Leadership Computing Facility at the Oak Ridge National Laboratory, which is supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC05-00OR22725.
Keywords
- cation hydration
- dipolar orientation polarization
- lipid bilayers
- long-term potentiation
- memcapacitance
- nonequilibrium steady states
- plasticity