Screening of a phage display library of exendin-4 mutants with the extracellular domain of rat GLP-1 receptor

A phage display library of exendin-4 mutants was screened with the extracellular domain of rat glucagon-like peptide 1 receptor as the target. A novel variant of exendin-4 with higher affinity for the receptor fraction than that of the wild type was identified. The increased affinity was attributed to the substitution of Glu 16 by Val 16. Although the substitution probably caused an increased entropic cost to the helix region, the linker around Val 16 is more flexible resulting in the increase of affinity for the receptor.