4.5 Article

Direct Measurement of Charge Reversal on Lipid Bilayers Using Heterodyne-Detected Second Harmonic Generation Spectroscopy

Journal

JOURNAL OF PHYSICAL CHEMISTRY B
Volume 124, Issue 4, Pages 641-649

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcb.9b09341

Keywords

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Funding

  1. National Science Foundation under the Center for Sustainable Nanotechnology [CHE-1503408]
  2. U.S. National Science Foundation (NSF) under its graduate fellowship research program (GRFP) award
  3. Northwestern University Presidential Fellowship
  4. Dow Chemical Company Professorship
  5. Alexander von Humboldt Foundation

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We report the detection of charge reversal induced by the adsorption of an aqueous cationic polyelectrolyte, poly(allylamine hydrochloride) (PAH), to supported lipid bilayers (SLBs) used as idealized model biological membranes. Through the use of an alpha-quartz reference crystal, we quantify the total interfacial potential at the interface in absolute units using heterodyne-detected second harmonic generation (HD-SHG) as an optical voltmeter. This quantification is made possible by isolating the phase-shifted potential-dependent third-order susceptibility from other contributions to the total SHG response. We detect the sign and magnitude of the surface potential and the point of charge reversal at buried interfaces without prior information or complementary data. Isolation of the second-order susceptibility contribution from the overall SHG response allows us to directly characterize the Stern and diffuse layers over single-component SLBs. We apply the method to SLBs formed from three different zwitterionic lipids having different gel-to-fluid phase transition temperatures (T-m's). We determine whether the surface potential changes with the physical phase state (gel, transitioning, or fluid) of the SLB. Furthermore, we incorporate 20% of negatively charged lipids to the zwitterionic SLB to investigate how the surface potential and the second-order nonlinear susceptibility chi((2)) change with surface charge.

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