Protein Surface Recognition by Synthetic Receptors: A Route to Novel Submicromolar Inhibitors for α-Chymotrypsin
journal contributionposted on 28.12.1998, 00:00 by Hyung Soon Park, Qing Lin, Andrew D. Hamilton
A family of synthetic receptors for protein surface recognition has been prepared. The receptors are based on a design in which four peptide loops are arrayed around a central calilxarene core. By varying the sequence of the loop regions a range of differently functionalized receptor surfaces approximately 450 Å2 in area can be prepared. From this family we have identified potent inhibitors of chymotrypsin that function by binding to the surface of the protein. The most potent of these (1) shows slow binding kinetics in an analogous manner to several of the natural protein proteinase inhibitors. Detailed kinetic analysis showed 1 to be a competitive inhibitor with Ki and Ki* values of 0.81 and 0.11 μM, respectively.