Abstract
This study examined the biological properties of a novel GLP-1 peptide, (Val(8) )GLP-1-Glu-PAL, engineered with an Ala(8) →Val(8) substitution and additional incorporation of a C(16) fatty acid moiety at Lys(26) via a glutamic acid linker. GLP-1 underwent 75 % degradation by DPP-IV over 8 h, whereas (Val(8) )GLP-1 and (Val(8) )GLP-1-Glu-PAL remained intact. All GLP-1 peptides significantly stimulated insulin secretion at 5.6 mM (1.3- to 4.9-fold, p
| Original language | English |
|---|---|
| Pages (from-to) | 595-602 |
| Journal | ChemMedChem |
| Volume | 8 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published (in print/issue) - 1 Mar 2013 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Fingerprint
Dive into the research topics of '(Val(8) )GLP-1-Glu-PAL: a GLP-1 Agonist That Improves Hippocampal Neurogenesis, Glucose Homeostasis, and β-Cell Function in High-Fat-Fed Mice.'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver