cmdc.202100315.pdf (1.21 MB)
Fluorescent amino acid initiated de novo cyclic peptides for the label-free assessment of cell permeability.
journal contributionposted on 2021-11-03, 10:57 authored by Yuteng Wu, M Teresa Bertran, James Rowley, Ewen DD Calder, Dhira Joshi, Louise J Walport
The major obstacle in applying peptides to intracellular targets is their low inherent cell permeability. Standard approaches to attach a fluorophore (e.g. FITC, TAMRA) can change the physicochemical properties of the parent peptide and influence their ability to penetrate and localize in cells. We report a label-free strategy for evaluating the cell permeability of cyclic peptide leads. Fluorescent tryptophan analogues 4-cyanotryptophan (4CNW) and beta-(1-azulenyl)-L-alanine (AzAla) were incorporated into in vitro translated macrocyclic peptides by initiator reprogramming. We then demonstrate these efficient blue fluorescent emitters are good tools for monitoring peptide penetration into cells.