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Alanine mutations of E124 3.33 and R283 6.55 nearly abolished the binding of ghrelin-A2 and the ghrelin-induced receptor activity, indicating the critical role of the salt bridge in maintaining the integrity of the bifurcated binding pockets, and thus affecting ghrelin binding and receptor activation (Supplementary Figs
Greater potency and greater stability from one structural change, which is why the constrained-cyclic approach recurs throughout peptide medicinal chemistry
Commonly used reducing agents include TCEP, DTT, and bME
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