Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Localization and synthesis of an insulin-binding region on human insulin receptor

Journal Article · · Journal of Protein Chemistry; (USA)
DOI:https://doi.org/10.1007/BF01025313· OSTI ID:6795723
; ;  [1]
  1. Baylor College of Medicine, Houston, TX (USA)
Seven regions of the alpha subunit of human insulin receptor (HIR) were synthesized and examined for their ability to bind radioiodinated insulin. A peptide representing one of these regions (namely, residues alpha 655-670) exhibited a specific binding activity for insulin. In quantitative radiometric titrations, the binding curves of {sup 125}I-labeled insulin to adsorbents of peptide alpha 655-670 and of purified placental membrane were similar or superimposable. The binding of radioiodinated insulin to peptide or to membrane adsorbents was completely inhibited by unlabeled insulin, and the inhibition curves indicated that the peptide and the membrane on the adsorbents had similar affinities. Synthetic peptides that were shorter (peptide alpha 661-670) or longer (peptide alpha 651-670) than the region alpha 655-670 exhibited lower insulin-binding activity. It was concluded that an insulin-binding region in the HIR alpha subunit resides within residues alpha 655-670. The results do not rule out the possibility that other regions of the alpha subunit may also participate in binding of HIR to insulin, with the region described here forming a face within a larger binding site.
OSTI ID:
6795723
Journal Information:
Journal of Protein Chemistry; (USA), Journal Name: Journal of Protein Chemistry; (USA) Vol. 9:2; ISSN JPCHD; ISSN 0277-8033
Country of Publication:
United States
Language:
English