Reversible PEGylation of peptide YY3-36 prolongs its inhibition of food intake in mice

FEBS Lett. 2005 Apr 25;579(11):2439-44. doi: 10.1016/j.febslet.2005.03.044.

Abstract

Administration of peptide YY(3-36) (PYY(3-36)) to fasting humans or mice shortly before re-feeding effectively reduced their food intake, but PYY(3-36) exhibited a functional half-life of only approximately 3 h. Attachment of poly(ethylene glycol) to proteins and peptides (PEGylation) prolongs their half-life in vivo, but completely inactivated PYY(3-36). We developed a reversibly PEGylated PYY(3-36) derivative by coupling it to a 40 kDa PEG through a spontaneously cleavable linker. The resulting conjugate (PEG(40)-FMS-PYY(3-36)) gradually released unmodified PYY(3-36) in vivo, exhibiting an eightfold increase in its functional half-life, to approximately 24h. This long-acting PYY(3-36) pro-drug may serve as an effective means for controlling food intake in humans.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Dose-Response Relationship, Drug
  • Feeding Behavior / drug effects*
  • Hydrolysis
  • Kinetics
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Peptide Fragments
  • Peptide YY / blood
  • Peptide YY / chemistry*
  • Peptide YY / pharmacology*
  • Polyethylene Glycols / chemistry*
  • Polyethylene Glycols / pharmacology*
  • Time Factors

Substances

  • Peptide Fragments
  • Peptide YY
  • peptide YY (3-36)
  • Polyethylene Glycols