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Engineering nanometre-scale coherence in soft matter.

Chaoren Liu1, Limin Xiang2, Yuqi Zhang1

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Electronic delocalization in DNA is supported by guanine (G) runs. This study reveals an even-odd orbital-symmetry rule governing charge transport, enabling nanometre-scale coherence in DNA.

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Area of Science:

  • Molecular electronics
  • Biophysics
  • Materials science

Background:

  • Electronic delocalization in polymers can be hindered by environmental heterogeneity.
  • Persistent delocalization occurs when environmental effects on redox potential are smaller than monomer-monomer interactions.

Purpose of the Study:

  • To investigate charge transport and delocalization in guanine (G) runs within double-stranded DNA.
  • To explore the role of G-G interactions and orbital symmetry in DNA charge transport.

Main Methods:

  • Development of a molecular-resolution model for charge transport in DNA.
  • Utilizing break-junction experiments to test theoretical predictions.

Main Results:

  • Guanine runs in double-stranded DNA support delocalization over 4-5 bases.
  • Charge transport coherence follows an even-odd orbital-symmetry rule.
  • Weakening inter-strand G-block interactions enhances resistance oscillations.

Conclusions:

  • DNA sequence can be engineered to control the balance between coherent and incoherent charge transport.
  • Tailored orbital symmetry and structural fluctuations can achieve multi-nanometre coherent transport in DNA.
  • This principle is applicable to soft-matter assemblies, potentially mimicking charge transport in proteins.