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

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 ∼3h. Attachment of poly(ethylene glycol) to proteins and peptides (PEGylation) prolongs their half-life in vivo,...

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Veröffentlicht in:FEBS letters 2005-04, Vol.579 (11), p.2439-2444
Hauptverfasser: Shechter, Yoram, Tsubery, Haim, Mironchik, Marina, Rubinstein, Menachem, Fridkin, Mati
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Sprache:eng
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Zusammenfassung: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 ∼3h. 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 40kDa 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 ∼24h. This long-acting PYY3-36 pro-drug may serve as an effective means for controlling food intake in humans.
ISSN:0014-5793
1873-3468
DOI:10.1016/j.febslet.2005.03.044