Self-Assembly of Fluorinated Sugar Amino Acid Derived α,γ-Cyclic Peptides into Transmembrane Anion Transport

Syntheses of fluorinated sugar amino acid derived α, γ -cyclic tetra- and hexapeptides are reported. The IR, NMR, ESI-MS, CD, and molecular modeling studies of cyclic tetra- and hexapeptides showed C 2 and C 3 symmetric flat oval- and triangular-ring shaped β-strand conformations, respectively, which appear to self-assemble into nanotubes. The α,γ -cyclic hexapeptide ( EC 50 = 2.14 μM) is found to be a more efficient ion transporter than α, γ -cyclic tetrapeptide ( EC 50 = 14.75 μM). The anion selectivity and recognition of α, γ -cyclic hexapeptide with NO 3 – ion is investigated.