Stability of the O-octanoyl group of rat ghrelin during chemical synthesis: Counter-ion-dependent alteration of an ester bond breakage

Stability of the O-octanoyl group of rat ghrelin during chemical synthesis: Counter-ion-dependent alteration of an ester bond breakage
January 2003
Masanori Ishimaru1, Kumiko Yoshizawa-Kumagaye1, Shigeru Kubo1, Tetsuya Kitani1, Naoyoshi- Chino2 , Kenji Kangawa3 and Terutoshi Kimura1
Letters in Peptide Science
Issue: Volume 10, Number 1
SpringerLink
(1) Peptide Institute, Inc., 4-1-2 Ina, Minoh, Osaka, Japan
(2) Peptide Institute, Inc., 4-1-2 Ina, Minoh, Osaka, Japan
(3) National Cardiovascular Center Research Institute, 5-7-1 Fujishirodai, Suita, Osaka, Japan
Abstract Rat ghrelin, a 28-amino acid residue peptide with an octanoyl group at the side chain of Ser3, was synthesized chemically by applying Fmoc/tBu strategy. An ester linkage between octanoic acid and the hydroxyl function of Ser3 was found to be maintained without serious damage during the final deprotection with trifluoroacetic acid (TFA). The most notable finding was the counter-ion-dependent stability change of the octanoyl moiety in the molecule. After consolidation of the counter-ion to TFA (TFA form), the octanoyl group persisted stably upon dissolution in water, whereas in the case of the acetate-form peptide, both de-octanoylation and dehydration (formation of the dehydro-Ala residue) occurred in aqueous solution at the same Ser3 residue. The amounts of these degraded products varied with factors such as solvent, temperature and times of lyophilization. These experimental findings lay the basis for performing the bioassay of ghrelin, which has an octanoyl moiety involved in its numerous biological activities thus far revealed.
acylated peptide - chemical synthesis - counter-ion-dependent stability - de-acylation - dehydration - octanoyl group - post-translational modification
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