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Key advancements in peptide technology for triple receptor agonism: Application of computational modeling to peptide-receptor binding Fatty acid substitution for extended stability and duration -helical design for superior receptor fit Structure-based design to hone drug action and safety Engineering peptides that simultaneously bind and stimulate multiple receptors Clinical Implications With retatrutide, a triple receptor agonist that has been studied in clinical trials for obesity and metabolic diseases, including type 2 diabetes and MASLD

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As a complementary approach to probing the Arr pathway, we quantified agonist-induced GLP-1R internalization using human embryonic kidney (HEK) 293 cells stably expressing a fluorogen-activated protein (FAP)-tagged version of the human GLP-1R (Fig

Studied primarily for tissue repair, angiogenic effects, and growth factor signaling