Here, we analyze the biophysical properties of the SARS-CoV-2 S-glycoprotein binding, on model surfaces and on living cells, to ACE2 receptors using force–distance (FD) curve-based atomic force microscopy (FD-curve-based AFM). We extract the kinetics and thermodynamics of the interactions established in vitro, and compare the binding properties of both the S1 subunit and RBD. Next, we test short ACE2-derived peptides targeting the viral S glycoprotein as potent binding inhibitor peptides and observe a significant reduction in the binding properties.
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We are testing others peptides

