A Water-Soluble Peptoid that Can Extract Cu from Metallothionein via Selective Recognition.

Selective binding of Cu in water medium by a synthetic chelator is a promising therapeutic approach towards the treatment of various diseases including cancer. Chelation of Cu is well exercised, however water-soluble synthetic chelators that can selectively bind Cu from a pool of competing metal ions at very high excess and/or can extract Cu from a protein are hardly reported. Herein we describe the design and synthesis of an acetylated peptoid-N-substituted glycine trimer-that incorporates a picolyl group at the N-terminal, a non-coordinating but structurally directing bulky chiral phenylethyl group at the C-terminus and a modified 2,2'-bipyridine group (PCA-Nspe), which selectively binds Cu to form a water-soluble complex. We further demonstrate that the selectivity of PCA-Nspe to Cu is thermodynamically driven, leading to specific binding of Cu in an aqueous solution containing up to 60-fold excess of other biologically relevant metal ions such as Zn , Co , Mn , Ca , Mg , K and Na . Based on spectroscopic data and DFT calculations of PCA-Nspe as well as of a control peptoid having an achiral benzyl group instead of the phenylethyl side chain, we could suggest that the chiral and bulkier phenylethyl group at the C-terminus controls the preorganization of the two ligands, and this might play a role in the selectivity of PCA-Nspe. Significantly, we show that PCA-Nspe can extract Cu from the natural copper binding protein metallothionein.