Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2053312 | FEBS Letters | 2005 | 6 Pages |
Abstract
Administration of peptide YY3-36 (PYY3-36) to fasting humans or mice shortly before re-feeding effectively reduced their food intake, but PYY3-36 exhibited a functional half-life of only ∼3 h. Attachment of poly(ethylene glycol) to proteins and peptides (PEGylation) prolongs their half-life in vivo, but completely inactivated PYY3-36. We developed a reversibly PEGylated PYY3-36 derivative by coupling it to a 40 kDa PEG through a spontaneously cleavable linker. The resulting conjugate (PEG40–FMS–PYY3-36) gradually released unmodified PYY3-36 in vivo, exhibiting an eightfold increase in its functional half-life, to ∼24 h. This long-acting PYY3-36 pro-drug may serve as an effective means for controlling food intake in humans.
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Authors
Yoram Shechter, Haim Tsubery, Marina Mironchik, Menachem Rubinstein, Mati Fridkin,