The peptide display library employs NNS mutagenesis, if that is of any help. What techniques can be used to show interaction and hence screen peptide ligands?
Thanks Farkas for your answer, but I had already considered this option, as in successive rounds of MACS and FACS but the issue here for this approach is that the receptor needs to be in soluble form attached to a bead, which is not possible in my case as the receptor is an integral membrane protein and hence cannot be purified in its original conformation. is here any way that i can study the interaction of ligands with the receptor in its original conformation??