Molecularly Resolved Images of Peptide-Functionalized Gold

Nov 12, 2012 - 0.75 mM 1-decanethiol (DT) for 24 h at room temperature. (All chemicals were .... Award at the Scientific Interface from the Burroughs ...
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Molecularly Resolved Images of Peptide-Functionalized Gold Surfaces by Scanning Tunneling Microscopy Annette F. Raigoza and Lauren J. Webb* Department of Chemistry and Biochemistry, Center for Nano- and Molecular Science and Technology, and Institute for Cell and Molecular Biology, The University of Texas at Austin, 1 University Station A5300, Austin, Texas 78712, United States ABSTRACT: Peptide-terminated monolayers were formed through a Huisgen cycloaddition reaction between an α-helical peptide containing two propargylglycine unnatural functional groups 20 Å apart and an alkanethiol self-assembled monolayer (SAM) on a gold surface containing 25% surface density of reactive azide terminal groups. The azide- and peptide-terminated surfaces were imaged by scanning tunneling microscopy (STM) using a low tunneling current of 10 pA. On the peptide-terminated surface, oblong features ∼30 Å long and ∼20 Å wide were observed and attributed to individual surface-bound αhelical peptides oriented parallel to the gold surface. These features covered an area of the surface corresponding to a density of 0.11 ± 0.01 peptides nm−2, compared with a theoretical density of ∼0.14 peptides nm−2 for a fully reacted surface. Finally, no evidence of peptide aggregation was observed on either short (