California Institute for Biomedical Research (Calibr), 11119 N. Torrey Pines Road, La Jolla, CA, 92037, USA.
Angew Chem Int Ed Engl. 2016 Sep 26;55(40):12475-8. doi: 10.1002/anie.201606321. Epub 2016 Sep 6.
Glucagon-like peptide-1 (GLP-1) receptor (GLP-1R), glucagon (GCG) receptor (GCGR), and glucose-dependent insulinotropic polypeptide (GIP, also known as gastric inhibitory polypeptide) receptor (GIPR), are three metabolically related peptide hormone receptors. A novel approach to the generation of multifunctional antibody agonists that activate these receptors has been developed. Native or engineered peptide agonists for GLP-1R, GCGR, and GIPR were fused to the N-terminus of the heavy chain or light chain of an antibody, either alone or in pairwise combinations. The fusion proteins have similar in vitro biological activities on the cognate receptors as the corresponding peptides, but circa 100-fold longer plasma half-lives. The GLP-1R mono agonist and GLP-1R/GCGR dual agonist antibodies both exhibit potent effects on glucose control and body weight reduction in mice, with the dual agonist antibody showing enhanced activity in the latter.
胰高血糖素样肽-1 (GLP-1) 受体 (GLP-1R)、胰高血糖素 (GCG) 受体 (GCGR) 和葡萄糖依赖性胰岛素释放多肽 (GIP,也称为胃抑制多肽) 受体 (GIPR) 是三种代谢相关的肽激素受体。已经开发出一种生成能够同时激活这些受体的多功能抗体激动剂的新方法。将天然或工程化的 GLP-1R、GCGR 和 GIPR 肽激动剂融合到抗体的重链或轻链的 N 端,单独或成对组合。融合蛋白在体外对相应受体具有与相应肽相似的生物学活性,但血浆半衰期长约 100 倍。GLP-1R 单激动剂和 GLP-1R/GCGR 双激动剂抗体均在小鼠中表现出对葡萄糖控制和体重减轻的有效作用,双激动剂抗体在后一种作用中表现出增强的活性。