Solid-supported lipid bilayers - A versatile tool for the structural and functional characterization of membrane proteins

Methods. 2020 Aug 1:180:56-68. doi: 10.1016/j.ymeth.2020.09.005. Epub 2020 Sep 11.

Abstract

The cellular membrane is central to the development of single-and multicellular life, as it separates the delicate cellular interior from the hostile environment. It exerts tight control over entry and exit of substances, is responsible for signaling with other cells in multicellular organisms and prevents pathogens from entering the cell. In the case of bacteria and viruses, the cellular membrane also hosts the proteins enabling invasion of the host organism. In a very real sense therefore, the cellular membrane is central to all life. The study of the cell membrane and membrane proteins in particular has therefore attracted significant attention. Due to the enormous variety of tasks performed by the membrane, it is a highly complex and challenging structure to study. Ideally, membrane components would be studied in isolation from this environment, but unlike water soluble proteins, the amphiphilic environment provided by the cellular membrane is key to the structure and function of the cell membrane. Therefore, model membranes have been developed to provide an environment in which a membrane protein can be studied. This review presents a set of tools that enable the comprehensive characterization of membrane proteins: electrochemical tools, surface plasmon resonance, neutron scattering, the surface forces apparatus and atomic force microscopy are discussed, with a particular focus on experimental technique and data evaluation.

Keywords: Biophysics; Membrane proteins; Model membranes; Structural biology.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Dielectric Spectroscopy / methods*
  • Electrochemistry / methods*
  • Ion Channels / chemistry*
  • Lipid Bilayers / chemistry*
  • Membrane Proteins / chemistry*
  • Membranes, Artificial
  • Microscopy, Atomic Force / methods*
  • Neutrons
  • Surface Plasmon Resonance / instrumentation
  • Surface Plasmon Resonance / methods*

Substances

  • Ion Channels
  • Lipid Bilayers
  • Membrane Proteins
  • Membranes, Artificial