Shallow conductance decay along the heme array of a single tetraheme protein wire.
Kavita GargZdeněk FuteraXiaojing WuYongchan JeongRachel ChiuVarun Chittari PisharamTracy Q HaAlbert C AragonèsJessica H van WonderenJulea N ButtJochen BlumbergerIsmael Diez-PerezPublished in: Chemical science (2024)
Multiheme cytochromes (MHCs) are the building blocks of highly conductive micrometre-long supramolecular wires found in so-called electrical bacteria. Recent studies have revealed that these proteins possess a long supramolecular array of closely packed heme cofactors along the main molecular axis alternating between perpendicular and stacking configurations (TST = T-shaped, stacked, T-shaped). While TST arrays have been identified as the likely electron conduit, the mechanisms of outstanding long-range charge transport observed in these structures remain unknown. Here we study charge transport on individual small tetraheme cytochromes (STCs) containing a single TST heme array. Individual STCs are trapped in a controllable nanoscale tunnelling gap. By modulating the tunnelling gap separation, we are able to selectively probe four different electron pathways involving 1, 2, 3 and 4 heme cofactors, respectively, leading to the determination of the electron tunnelling decay constant along the TST heme motif. Conductance calculations of selected single-STC junctions are in excellent agreement with experiments and suggest a mechanism of electron tunnelling with shallow length decay constant through an individual STC. These results demonstrate that an individual TST motif supporting electron tunnelling might contribute to a tunnelling-assisted charge transport diffusion mechanism in larger TST associations.
Keyphrases
- solar cells
- high resolution
- high throughput
- electron microscopy
- high density
- electron transfer
- signaling pathway
- molecular dynamics simulations
- molecular dynamics
- mass spectrometry
- density functional theory
- small molecule
- quantum dots
- binding protein
- liquid chromatography
- solid phase extraction
- amino acid
- energy transfer