Dulaglutide is a 63-kDa fusion protein (two proteins joined into one large molecule). It combines a modified human GLP-1(7-37) (a gut hormone that controls blood sugar; changes: Ala8Gly, Gly22Glu, Arg36Gly) with the Fc part of a modified human IgG4 antibody (a section that helps proteins last in the blood), joined by a 13-amino acid linker (GGGGGGGSGGGGSG). The result is a two-part (homodimeric) structure. This design lets the body recycle it through FcRn (a recycling receptor), giving a long half-life (~5 days) while it still strongly activates the GLP-1 receptor. Dulaglutide switches on GLP-1 receptors on pancreatic beta cells (insulin-making cells) to release insulin only when blood sugar is high. It lowers glucagon (a hormone that raises blood sugar) from alpha cells when blood sugar is high, slows stomach emptying through signals along the vagus nerve, and switches on GLP-1 receptors in the hypothalamus (the brain's appetite center) to make you feel full and eat less.