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Hg(II) Binding to Thymine Bases in DNA.

Susan Nehzati1, Anne O Summers2, Natalia V Dolgova1

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Mercury(II) ions bind directly to DNA, specifically to thymine bases in AT-rich regions. This study reveals the preferred binding mode and its characteristic X-ray signature, advancing our understanding of mercury toxicity mechanisms.

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Area of Science:

  • Environmental chemistry
  • Biochemistry
  • Toxicology

Background:

  • Mercury compounds are highly toxic, impacting biological processes through poorly understood mechanisms.
  • Mercury(II) ions (Hg(II)) exhibit a unique ability to directly bind to DNA, forming interstrand cross-links in thymine bases within AT-rich DNA sequences.

Purpose of the Study:

  • To investigate the interaction between Hg(II) and thymine, the preferred binding mode, and the structural consequences for DNA.
  • To characterize the X-ray spectroscopic signature of Hg(II)-thymine binding using a model compound.

Main Methods:

  • Small molecule X-ray diffraction
  • X-ray spectroscopies
  • Computational chemistry
  • 1-methylthymine as a model system

Main Results:

  • The energetically preferred binding site for Hg(II) on thymine in DNA is the N3 position.
  • Hg(II) binding to adjacent thymine nucleotides causes minor DNA distortions, with a preferred twisted geometry (32-43° torsion angle).
  • Bis-thymine coordination of Hg(II) yields a distinct X-ray spectroscopic signature, differentiating it from other known Hg(II) biological binding modes.

Conclusions:

  • This research clarifies a significant biological interaction of Hg(II) with DNA, specifically targeting thymine bases.
  • The identified X-ray spectroscopic signature provides a tool for detecting Hg(II)-DNA binding in complex biological samples like cells and tissues.
  • The findings lay the groundwork for future investigations into the mechanisms underlying mercury toxicity.