The
lack of solubility in water and the formation of aggregates
hamper many opportunities for technological exploitation of C60. Here, different peptides were designed and synthesized
with the aim of monomolecular dispersion of C60 in water.
Phenylalanines were used as recognizing moieties, able to interact
with C60 through π–π stacking, while
a varying number of glycines were used as spacers, to connect the
two terminal phenylalanines. The best performance in the dispersion
of C60 was obtained with the FGGGF peptidic nanotweezer
at a pH of 12. A full characterization of this adduct was carried
out. The peptides disperse C60 in water with high efficiency,
and the solutions are stable for months both in pure water and in
physiological environments. NMR measurements demonstrated the ability
of the peptides to interact with C60. AFM measurements
showed that C60 is monodispersed. Electrospray ionization
mass spectrometry determined a stoichiometry of C60@(FGGGF)4. Molecular dynamics simulations showed that the peptides
assemble around the C60 cage, like a candy in its paper
wrapper, creating a supramolecular host able to accept C60 in the cavity. The peptide-wrapped C60 is fully biocompatible
and the C60 “dark toxicity” is eliminated.
C60@(FGGGF)4 shows visible light-induced reactive
oxygen species (ROS) generation at physiological saline concentrations
and reduction of the HeLa cell viability in response to visible light
irradiation.
Of all the amino acids, the surface of π‐electron conjugated carbon nanoparticles has the largest affinity for tryptophan, followed by tyrosine, phenylalanine, and histidine. In order to increase the binding of a protein to a fullerene, it should suffice to mutate a residue of the site that binds to the fullerene to tryptophan, Trp. Computational chemistry shows that this intuitive approach is fraught with danger. Mutation of a binding residue to Trp may even destabilize the binding because of the complicated balance between van der Waals, polar and non‐polar solvation interactions.
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