Role of the carboxyl-terminal region, di-leucine motif and cysteine residues in signalling and internalization of vasopressin V1a receptor

FEBS Lett. 1999 Oct 29;460(2):303-8. doi: 10.1016/s0014-5793(99)01360-5.

Abstract

The structural requirements for internalization and signalling of the vasopressin V1a receptor were investigated in stably transfected HEK-293 cells. Removal of the 51 C-terminal amino acids did not affect vasopressin binding, calcium signalling, heterologous desensitization or internalization of the receptor. Deletion of 14 additional amino acids reduced vasopressin-dependent calcium increase and impaired receptor internalization. Substitution of cysteines 371-372 did not affect intracellular signalling, but decreased endocytosis by 26%. Substitution of the 361-362 leucine by alanine residues reduced by 56% V1a receptor sequestration without affecting calcium signalling. These results indicate that di-cysteine and mostly di-leucine motifs present in the C-terminal region of the V1a receptor are involved in its internalization.

MeSH terms

  • Calcium / metabolism
  • Cell Line
  • Cysteine / physiology*
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • Fluorescent Antibody Technique
  • Humans
  • Kinetics
  • Leucine / physiology*
  • Models, Biological
  • Mutagenesis
  • Protein Binding
  • Receptors, Vasopressin / chemistry
  • Receptors, Vasopressin / metabolism*
  • Signal Transduction
  • Time Factors
  • Transfection
  • Vasopressins / pharmacology

Substances

  • Receptors, Vasopressin
  • Vasopressins
  • Leucine
  • Cysteine
  • Calcium