Molecular site for nucleotide binding on an ATP-sensitive renal K+ channel (ROMK2)

Am J Physiol. 1996 Aug;271(2 Pt 2):F275-85. doi: 10.1152/ajprenal.1996.271.2.F275.

Abstract

ATP-sensitive, inwardly rectifying K+ channels are present in apical membranes of the distal nephron and play a major role in K+ recycling and secretion. The cloned renal K+ channel, ROMK1, is a candidate for the renal epithelial K+ channel, since it shares many functional characteristics with the native channel. Additionally, ROMK1 contains a putative carboxy-terminal ATP-binding site. Although ROMK1 channel activity could be reactivated by cytosolic Mg-ATP after rundown, the role of nucleotides in channel gating was less certain. We now show that an alternatively spliced transcript of the ROMK channel gene, ROMK2, which encodes a K+ channel with a truncated amino terminus, expresses an ATP-regulated and ATP-sensitive K+ channel (IKATP). Differences in the amino terminus of ROMK isoforms alters the sensitivity of the channel-gating mechanism to ATP. To test whether ATP sensitivity of renal IKATP is mediated by direct interaction of nucleotide, point mutation of specific residues within the ROMK2 phosphate loop (P-loop) were investigated. These either enhanced or attenuated the sensitivity to both activation and inhibition by Mg-ATP, thus demonstrating a direct interaction of nucleotide with the channel-forming polypeptide.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / pharmacology*
  • Amino Acid Sequence
  • Animals
  • Female
  • Kidney / metabolism*
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Nucleotides / metabolism*
  • Oocytes
  • Patch-Clamp Techniques
  • Potassium Channels / drug effects
  • Potassium Channels / genetics*
  • Potassium Channels / metabolism*
  • Xenopus

Substances

  • Nucleotides
  • Potassium Channels
  • Adenosine Triphosphate