Design, synthesis and biological evaluation of double fatty chain-modified glucagon-like peptide-1 conjugates

Bioorg Med Chem. 2021 Aug 15:44:116291. doi: 10.1016/j.bmc.2021.116291. Epub 2021 Jun 24.

Abstract

Twelve double fatty chains and Aib8-Arg34-GLP-1 (7-37) were designed and obtained by microwave-assisted solid-phase synthesis. Then, twelve conjugates of Aib8-Arg34-GLP-1 (7-37) were synthesized in 1% triethylamine aqueous solution. Conjugates 2, 3, 6, 7, 10 and 11 showed better GLP-1 receptor activation potency than semaglutide. However, conjugates 2, 6 and 10 showed slightly worse glucose-lowering effects in vivo than semaglutide but better effects than conjugates 3, 7 and 11. The CD spectra of conjugates 2, 6 and 10 indicated that they had the same secondary structure as liraglutide and semaglutide. The receptor affinity results for conjugates 2, 6 and 10 measured by SPR (surface plasmon resonance) showed that conjugate 2 had higher receptor affinity than conjugates 6 and 10. In addition, albumin binding assays indicated that double fatty acid chains had obvious synergistic effects compared with single fatty acid chains. In conclusion, the structure-activity relationship of different side chains was summarized and one candidate, conjugate 2, was screened.

Keywords: Aib(8)-Arg(34)-GLP-1; Glucose-lowering; SPR; Structure–activity relationship; Synergistic effects.

MeSH terms

  • Amino Acids / chemistry
  • Drug Design*
  • Esters / chemical synthesis
  • Esters / chemistry
  • Glucagon-Like Peptide 1 / chemical synthesis
  • Glucagon-Like Peptide 1 / chemistry*
  • Molecular Structure
  • Solid-Phase Synthesis Techniques
  • Succinimides / chemical synthesis
  • Succinimides / chemistry

Substances

  • Amino Acids
  • Esters
  • Succinimides
  • succinimide
  • Glucagon-Like Peptide 1