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Lipid modulation of ion channels through specific binding sites
Authors:JA Poveda  AM GiudiciML Renart  ML MolinaE Montoya  A Fernández-CarvajalG Fernández-Ballester  JA EncinarJM González-Ros
Institution:Instituto de Biología Molecular y Celular, Universidad Miguel Hernández, E-03202 Elche, Spain
Abstract:Ion channel conformational changes within the lipid membrane are a key requirement to control ion passage. Thus, it seems reasonable to assume that lipid composition should modulate ion channel function. There is increasing evidence that this implicates not just an indirect consequence of the lipid influence on the physical properties of the membrane, but also specific binding of selected lipids to certain protein domains. The result is that channel function and its consequences on excitability, contractility, intracellular signaling or any other process mediated by such channel proteins, could be subjected to modulation by membrane lipids. From this it follows that development, age, diet or diseases that alter lipid composition should also have an influence on those cellular properties. The wealth of data on the non-annular lipid binding sites in potassium channel from Streptomyces lividans (KcsA) makes this protein a good model to study the modulation of ion channel structure and function by lipids. The fact that this protein is able to assemble into clusters through the same non-annular sites, resulting in large changes in channel activity, makes these sites even more interesting as a potential target to develop lead compounds able to disrupt such interactions and hopefully, to modulate ion channel function. This Article is Part of a Special Issue Entitled: Membrane Structure and Function: Relevance in the Cell's Physiology, Pathology and Therapy.
Keywords:BK  big potassium channel  BN-PAGE  blue native polyacrylamide gel electrophoresis  Cav  voltage-gated calcium  CNG  cyclic nucleotide-gated channels  CRAC  cholesterol binding sites  CTD  cytoplasmic domain  ENaC  epithelial sodium channels  FRET    rster resonance energy transfer  GABAA  γ-aminobutyric acid-gated channel  GIRK  G protein-coupled inwardly-rectifying potassium channel  HCN  hyperpolarization-activated cyclic nucleotide-gated channel  hERG  human Ether-à  -go-go-Related Gene potassium channel  HOP  high opening probability pattern  IP3R  IP3-gated calcium release channels  KATP  potassium channel activated by intracellular ATP binding  KCNQ  potassium voltage-gated channel subfamily KQT  KcsA  potassium channel from Streptomyces lividans  Kir  inward-rectifier potassium channel  Kv  voltage-gated potassium channel  LOP  low opening probability pattern  MscL  large-conductance mechanosensitive channel  nAChR  nicotinic acetylcholine receptor  PA  phosphatidic acid  PC  phosphatidylcholine  PG  phosphatidylglycerol  PIP2  phosphatidylinositol 4  5-bisphosphate  PUFAs  polyunsaturated fatty acids  RyR  ryanodine-sensitive calcium release channels  SUR  sulfonylurea receptor  TMD  transmembrane domain  TRP  transient receptor potential channels  TRPL  transient receptor potential-like Drosophila phototransduction channels  VDAC  voltage-dependent anion channel
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