Cutting out the fat: Site-specific deacylation of an ion channel

J Biol Chem. 2020 Dec 4;295(49):16497-16498. doi: 10.1074/jbc.H120.016490.

Abstract

S-Acylation, a reversible post-translational lipid modification of proteins, controls the properties and function of various proteins, including ion channels. Large conductance Ca2+-activated potassium (BK) channels are S-acylated at two sites that impart distinct functional effects. Whereas the enzymes that attach lipid groups are known, the enzymes mediating lipid removal (i.e. deacylation) are largely unknown. Here, McClafferty et al. identify two enzymes, ABHD17a and ABHD17c, that excise BK channel lipid groups with remarkable precision. These findings lend insights into mechanisms that orchestrate the (de)acylation that fine-tunes ion channel function in physiology and disease.

Publication types

  • Comment

MeSH terms

  • Acylation
  • Ion Channels* / genetics
  • Large-Conductance Calcium-Activated Potassium Channels* / metabolism
  • Mutation
  • Potassium

Substances

  • Ion Channels
  • Large-Conductance Calcium-Activated Potassium Channels
  • Potassium