文摘
Peptide-terminated monolayers were formed through a Huisgen cycloaddition reaction between an 伪-helical peptide containing two propargylglycine unnatural functional groups 20 脜 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 脜 long and 20 脜 wide were observed and attributed to individual surface-bound 伪-helical peptides oriented parallel to the gold surface. These features covered an area of the surface corresponding to a density of 0.11 卤 0.01 peptides nm鈥?, compared with a theoretical density of 0.14 peptides nm鈥? for a fully reacted surface. Finally, no evidence of peptide aggregation was observed on either short (<10 nm) or long (100 nm) length scales.