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Validity and applicability of membrane model systems for studying interactions of peripheral membrane proteins with lipids
Authors:Aleksander Czogalla  Michał Grzybek  Walis JonesÜnal Coskun
Institution:Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD), Germany
Abstract:The cell membrane serves, at the same time, both as a barrier that segregates as well as a functional layer that facilitates selective communication. It is characterized as much by the complexity of its components as by the myriad of signaling process that it supports. And, herein lays the problems in its study and understanding of its behavior — it has a complex and dynamic nature that is further entangled by the fact that many events are both temporal and transient in their nature. Model membrane systems that bypass cellular complexity and compositional diversity have tremendously accelerated our understanding of the mechanisms and biological consequences of lipid–lipid and protein–lipid interactions. Concurrently, in some cases, the validity and applicability of model membrane systems are tarnished by inherent methodical limitations as well as undefined quality criteria. In this review we introduce membrane model systems widely used to study protein–lipid interactions in the context of key parameters of the membrane that govern lipid availability for peripheral membrane proteins. This article is part of a Special Issue entitled Tools to study lipid functions.
Keywords:AFM  atomic force microscopy  BLM  black lipid membrane  Cer  ceramide  CTX-B  B subunit of cholera-toxin  DPH  diphenylhexatriene  DTT  dithiothreitol  ER  endoplasmic reticulum  ESCRT  endosomal sorting complexes required for transport  FCS  fluorescence correlation spectroscopy  GM1  monosialotetrahexosylganglioside  GPMV  giant plasma membrane vesicle  GUV  giant unilamellar vesicle  ITC  isothermal titration calorimetry  ITO  indium tin oxide  Ld  liquid disordered  Lo  liquid ordered  LUV  large unilamellar vesicle  MLV  multilamellar vesicle  NEM  N-ethyl maleimide  PA  phosphatidic acid  PC  phosphatidylcholine  PE  phosphatidylethanolamine  PEG  polyethylene glycol  PFA  paraformaldehyde  PI  phosphatidylinositol  PIP  phosphatidylinositol phosphate  PS  phosphatidylserine  PVDF  polyvinylidene difluoride  SLB  supported lipid bilayer  SM  sphingomyelin  SPR  surface plasmon resonance  SUV  small unilamellar vesicle  TIRF  total internal reflection fluorescence  TLC  thin layer chromatography
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