A 310-helix single turn enforced by crosslinking of lysines with 1,1′-ferrocenedicarboxylic acid

Prior work has shown that covalently linking the side chains of amino acids in the i and i+3 and i and i+4 positions in a peptide will enforce a helical conformation. In this work the ability of an organometallic entity to enforce a helical conformation in a peptide was explored. The tetrapeptide Boc-Lys-Ala-Val-Lys-NHCH3 was prepared, then reacted with 1,1′-ferrocenedicarboxylic acid chloride. Reaction of the lysine side chain amines with the diacid chloride resulted in a metallacyclicpeptide (1) in which the two lysines are crosslinked via the ferrocene. The solution conformation of the metallacyclicpeptide (1) was studied using CD and NMR spectroscopy. The NMR methods employed were Karplus analysis of coupling constants, chemical shift changes of NH protons and ROESY data. The results show that the metallacyclicpeptide (1) adopts a single turn of the 310-helix conformation.

Reaction of Boc-Lys-Ala-Val-Lys-NHMe with 1,1′-ferrocenedicarboxylic acid chloride yields a cyclic species in which the lysine side chains are crosslinked and the peptide adopts a single turn of a 310-helix.Figure optionsDownload as PowerPoint slide