Exploiting Ultrashort α,β-Peptides in the Colloidal Stabilization of Gold Nanoparticles

Colloidal gold nanoparticles (GNPs) have found wide-ranging applications in nanomedicine due to their unique optical properties, ease of preparation, and functionalization. To avoid the formation of GNP aggregates in the physiological environment, molecules such as lipids, polysaccharides, or polymers are employed as GNP coatings. Here, we present the colloidal stabilization of GNPs using ultrashort alpha,beta-peptides containing the repeating unit of a diaryl beta(2,3)-amino acid and characterized by an extended conformation. Differently functionalized GNPs have been characterized by ultraviolet, dynamic light scattering, and transmission electron microscopy analysis, allowing us to define the best candidate that inhibits the aggregation of GNPs not only in water but also in mouse serum. In particular, a short tripeptide was found to be able to stabilize GNPs in physiological media over 3 months. This new system has been further capped with albumin, obtaining a material with even more colloidal stability and ability to prevent the formation of a thick protein corona in physiological media.

Automated summary

Researchers stabilized colloidal gold nanoparticles using ultrashort α,β-peptides, finding the best candidate that can stabilize GNPs in physiological media and further capped with albumin to enhance colloidal stability.