Characterization of a regulatory region in the N-terminus of rabbit kv1.3

Biochem Biophys Res Commun. 1998 Aug 19;249(2):492-8. doi: 10.1006/bbrc.1998.9122.

Abstract

The N-terminus of rabbit Kv1.3 contains a signal sequence which regulates expression of Kv1.3 proteins in the plasma membrane. Removal of an N-terminal region (aa3-39) produced an increase in expressed K+ current. Progressive deletion at the N-terminus demonstrated that the shortest deletion required for the elevation of K current is D6-34. Since the functional signal sequence must include both ends of the peptide segment aa6-34 where charged residues are densely distributed, it is conceivable that this N-terminal signal sequence is related to charge or its associated hydrophilicity. Removal of two charged residues (31R, 33E) through amino acid substitution which converts deletion construct D3-27 to D3-27* effectively raises the amplitude of expressed current, further indicating the importance of charged residues. With the use of a mutated dynamin and a soluble N-terminal peptide, we also revealed that the N-terminal signal sequence may not act through the endocytotic pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Chemical Phenomena
  • Chemistry, Physical
  • Dynamins
  • Electric Conductivity
  • Endocytosis
  • Female
  • GTP Phosphohydrolases / genetics
  • GTP Phosphohydrolases / pharmacology
  • Gene Deletion
  • Gene Expression
  • Kv1.3 Potassium Channel
  • Molecular Sequence Data
  • Mutagenesis
  • Oocytes
  • Peptide Fragments / chemistry*
  • Peptide Fragments / genetics
  • Potassium Channels / chemistry*
  • Potassium Channels / genetics
  • Potassium Channels / physiology
  • Potassium Channels, Voltage-Gated*
  • Protein Sorting Signals / chemistry
  • RNA, Complementary / genetics
  • Rabbits
  • Structure-Activity Relationship
  • Transfection
  • Xenopus laevis

Substances

  • Kv1.3 Potassium Channel
  • Peptide Fragments
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Protein Sorting Signals
  • RNA, Complementary
  • GTP Phosphohydrolases
  • Dynamins