Abstract

A chiral pentadecapeptide, l-gramicidine, has been shown to undergo specific adsorption onto gold surfaces modified by chiral amino acids, d- and l-methionine, upon adsorption in the liquid phase. There is a chiral recognition only between the slightly anionic l-peptide and the l-modified surface exhibiting cationic molecules. However, whatever the probe and target molecule charges, very weak recognition was observed between molecules of opposite chirality.

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