The isolation and sequencing of human gastric inhibitory peptide (GIP).
A J Moody, L Thim, I Valverde
Index: FEBS Lett. 172 , 142, (1984)
Full Text: HTML
Abstract
Human GIP 1-42 and fragments of human GIP corresponding to GIP 10-42, GIP 11-42, and GIP 17-42 were isolated from acid-ethanol extracts of human small intestines with the aid of an anti-GIP serum specific for the extreme C-terminal portion of the GIP molecule. The full sequence of human GIP has been established by Edman degradation of these peptides and fragments thereof by automatic gas-phase sequencing. Human GIP differs from porcine GIP at residues 18 and 34. The sequence of human GIP is thus: (Formula: see text) Amino acid residues 18 and 34 are Arg and Ser, respectively, in porcine GIP.
Related Compounds
Related Articles:
Long-term persistence of hormonal adaptations to weight loss.
2011-10-27
[N. Engl. J. Med. 365 , 1597-1604, (2011)]
Pleiotropic effects of GIP on islet function involve osteopontin.
2011-09-01
[Diabetes 60 , 2424-2433, (2011)]
2011-09-01
[Cent. Nerv. Syst. Agents Med. Chem. 11 , 210-222, (2011)]
2011-10-01
[Biol. Chem. 392 , 909-918, (2011)]
Synthesis of a 42 residue peptide corresponding to the entire amino acid sequence of human GIP.
1985-08-01
[Chem. Pharm. Bull. 33 , 3578, (1985)]