Co-assembly of Peptides and Carbon Nanodots: Sensitive Analysis of Transglutaminase 2

The structures assembled by peptides have attracted great attention due to their unique physicochemical properties. Moreover, the co-assembly of peptides with additional components can endow the structures with extended functions. In this work, we have explored the co-assembly of peptides and carbon nanodots (CNDs) by taking advantage of their non-covalent binding; thus, the obtained structure may show both the recognition capability of peptides and the catalytic activity of CNDs. Therefore, we have further used the assembled structure for the sensitive analysis of transglutaminase 2 with a low detection limit of 0.25 pg/mL. By simply replacing the peptide sequences or the nanomaterials, the strategy proposed in this work can be developed as a universal model to build the co-assemblies of peptides and nanomaterials, thus leading to their broader applications in biological and biomedical research.

Automated summary

This study explored the co-assembly of peptides and carbon nanodots (CNDs) using non-covalent binding, combining the recognition capability of peptides with the catalytic activity of CNDs. The assembled structure was used for sensitive analysis of transglutaminase 2 with a low detection limit of 0.25 pg/mL. This strategy can be developed into a universal model for building co-assemblies of peptides and nanomaterials, expanding their applications in biological and biomedical research.