Amino-acid interactions with the Au(111) surface: adsorption, band alignment, and interfacial electronic coupling.
Zdeněk FuteraPublished in: Physical chemistry chemical physics : PCCP (2021)
The charge transport properties of biological molecules like peptides and proteins are intensively studied for the great flexibility, redox-state variability, long-range efficiency, and biocompatibility of potential bioelectronic applications. Yet, the electronic interactions of biomolecules with solid metal surfaces, determining the conductivities of the biomolecular junctions, are hard to predict and usually unavailable. Here, we present accurate adsorption structures and energies, electronic band alignment, and interfacial electronic coupling data for all 20 natural amino acids computed using the DFT+Σ scheme based on the vdW-DF and OT-RSH functionals. For comparison, data obtained using the popular PBE functional are provided as well. Tryptophan, compared to other amino acids, is shown to be distinctly exceptional in terms of the electronic properties related to charge transport. Its high adsorption energy, frontier-orbital levels aligned relatively close to the Fermi energy of gold and strong interfacial electronic coupling make it an ideal candidate for facilitating charge transfer on such heterogeneous interfaces. Although the amino acids in peptides and proteins are affected by the structural interactions hindering their contact with the surface, knowledge of the single-molecule surface interactions is necessary for a detailed understanding of such structural effects and tuning of potential applications.
Keyphrases
- amino acid
- single molecule
- electron transfer
- molecular dynamics simulations
- electronic health record
- healthcare
- room temperature
- ionic liquid
- big data
- high resolution
- magnetic resonance imaging
- molecular dynamics
- atomic force microscopy
- molecular docking
- living cells
- density functional theory
- magnetic resonance
- computed tomography
- fluorescent probe
- pseudomonas aeruginosa
- risk assessment
- mass spectrometry
- drug induced
- high speed
- biofilm formation