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These data indicate that the disulfide bonds of both E127 ECD CQ211 ECL1 C and Q37 ECD CL379 ECL3 C are formed on the native protein in the absence of the antibody, strengthening the hypothesis that the current structure represents a physiologically relevant inactive conformation of GLP-1R

Therefore, the development of an oral delivery strategy for peptide GLP-1R agonists is expected to reduce these adverse effects and improve patient compliance and quality of life (Borner et al., 2020

[11] Shen Y, Prinyawiwatkul W, Xu Z

Tyr 10 Positions 10, 12, 13, and 14 of exenatide (full GLP-1R agonist) are different from those of GLP-1, suggesting that these residues are unimportant to GLP-1