Linaclotide is a hybrid
peptide design of the
E. coli heat-stable
enterotoxin (STa) and the endogenous peptide hormones
endogenous guanylin and
uroguanylin. It is a
synthetic tetradecapeptide (14
amino acid peptide) with the sequence CCEYCCNPACTGCY by one-letter abbreviation, or by three-letter abbreviation: H–
Cys1–Cys2–
Glu3–
Tyr4–Cys5–Cys6–
Asn7–
Pro8–
Ala9–Cys10–
Thr11–
Gly12–Cys13–Tyr14–OH However, the actual structure of linaclotide is not fully specified without the three
disulfide (R-S-S-R) bonds it contains, which are between Cys1 and Cys6, between Cys2 and Cys10, and between Cys5 and Cys13; these are shown in exaggerated fashion in the line-angle graphic showing the chemical bonds within and between each amino acid (and their stereochemistries, see the infobox, above right), and are represented using a one-letter abbreviations in the following additional schematic: A study in discovery synthesis reported that 2 of 14 strategies available to synthesize linaclotide were successful—the successful ones involving
trityl protection of all cysteines, or trityl protection of all cysteines except Cys1 and Cys6, which were protected with
tert-butylsulphenyl groups. The study also reported that solution-phase oxidation (disulfide formation) was advisable over solid-supported synthesis for linaclotide, and that the Cys1–Cys6 disulfide bridge was the most favored energetically. ==History==