Chemmedchem 2014-11-01

Position and length of fatty acids strongly affect receptor selectivity pattern of human pancreatic polypeptide analogues.

Veronika Mäde, Kathrin Bellmann-Sickert, Anette Kaiser, Jens Meiler, Annette G Beck-Sickinger

文献索引：ChemMedChem 9(11) , 2463-74, (2014)

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摘要

Pancreatic polypeptide (PP) is a satiety-inducing gut hormone targeting predominantly the Y4 receptor within the neuropeptide Y multiligand/multireceptor family. Palmitoylated PP-based ligands have already been reported to exert prolonged satiety-inducing effects in animal models. Here, we suggest that other lipidation sites and different fatty acid chain lengths may affect receptor selectivity and metabolic stability. Activity tests revealed significantly enhanced potency of long fatty acid conjugates on all four Y receptors with a preference of position 22 over 30 at Y1 , Y2 and Y5 receptors. Improved Y receptor selectivity was observed for two short fatty acid analogues. Moreover, [K(30)(E-Prop)]hPP2-36 (15) displayed enhanced stability in blood plasma and liver homogenates. Thus, short chain lipidation of hPP at key residue 30 is a promising approach for anti-obesity therapy because of maintained selectivity and a sixfold increased plasma half-life.© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

相关化合物

  • 甲酸
  • 乙腈
  • 三氟乙酸(TFA)
  • 棕榈酸
  • IC 锂标准品
  • 六氢吡啶
  • 茴香硫醚
  • 4-甲基苯硫酚
  • 乙二胺四乙酸
  • 1,2-乙二硫醇

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