https://www.selleckchem.com/pe....ptide/dulaglutide.ht
After the regeneration of the high-affinity cavities by washing out the bound lysozyme, the remaining thiol groups were reacted with 3-(2-pyridyldithio)propionic acid to introduce interacting groups, which produced capped MIPs. Comparing the capped and uncapped MIPs revealed that off-target protein binding was effectively suppressed by the capping treatment without any reduction in binding affinity (1.1 × 109 M-1). Further investigation revealed that the lysozyme concentration during the capping process is critical for the selectivit
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