Na+/i- symporter activity requires a small and uncharged amino acid residue at position 395

Orsolya Dohán, M. Verónica Gavrielides, Christopher Ginter, L. Mario Amzel, Nancy Carrasco

Research output: Contribution to journalArticle


Active iodide uptake in the thyroid is mediated by the Na+/I- symporter (NIS), a key plasma membrane glycoprotein. Several NIS mutations have been shown to cause I- transport defect, a condition that, if untreated, can lead to congenital hypothyroidism and, ultimately, cretinism. The study of I- transport defect-causing NIS mutations provides valuable insights into the structure-function and mechanistic properties of NIS. Here we report the thorough analysis of the G395R NIS mutation. We observed no I- uptake activity at saturating or even supersaturating external I- concentrations in COS-7 cells transiently transfected with G395R NIS cDNA, even though we demonstrated normal expression of G395R NIS and proper targeting to the plasma membrane. Several amino acid substitutions at position 395 showed that the presence of an uncharged amino acid residue with a small side chain at position 395 is required for NIS function, suggesting that glycine 395 is located in a tightly packed region of NIS. Substitutions of large amino acid residues at position 395 resulted in lower Vmax without affecting Km values for I- and Na+, suggesting that these residues hamper the Na+/I- coupling reaction.

Original languageEnglish (US)
Pages (from-to)1893-1902
Number of pages10
JournalMolecular Endocrinology
Issue number8
StatePublished - 2002

ASJC Scopus subject areas

  • Molecular Biology
  • Endocrinology

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