Study on the Interaction between Isatin-β-Thiosemicarbazone and Calf Thymus DNA by Spectroscopic Techniques

Parvaneh Pakravan1, Shahla Masoudian2

  • 1Department of Chemistry, Zanjan Branch, Islamic Azad University, Zanjan, Iran.

Insights

Isatin-β-thiosemicarbazone (IBT) intercalates into calf thymus DNA (CT-DNA), displacing Neutral Red dye. This DNA binding interaction is enthalpy-favored, confirmed by spectral and viscosity studies.

Area of Science:

  • Biophysical Chemistry
  • Molecular Interactions
  • Spectroscopy

Background:

  • Understanding drug-DNA interactions is crucial for developing new therapeutic agents.
  • Isatin derivatives have shown potential biological activities, warranting investigation into their molecular mechanisms.
  • Calf thymus DNA (CT-DNA) serves as a standard model for studying DNA-ligand interactions.

Purpose of the Study:

  • To investigate the binding mechanism of isatin-β-thiosemicarbazone (IBT) with calf thymus DNA (CT-DNA).
  • To characterize the thermodynamic and structural changes associated with IBT-CT-DNA complex formation.
  • To explore the potential of IBT as a DNA-interacting agent.

Main Methods:

  • UV-Vis absorption spectroscopy
  • Fluorescence spectroscopy (including quenching studies)
  • Viscosity measurements
  • Circular dichroism (CD) spectroscopy

Main Results:

  • IBT binds to CT-DNA via intercalation, with a binding constant K = 1.03×10(5) M⁻¹.
  • IBT displaces the Neutral Red (NR) dye from the NR-DNA complex.
  • Fluorescence quenching studies revealed binding constants (Kf) and approximately one binding site (n≈1).
  • Thermodynamic analysis indicated an enthalpy-favored and entropy-disfavored binding process.
  • CD spectral studies showed alterations in CT-DNA base stacking, supporting intercalation.

Conclusions:

  • Isatin-β-thiosemicarbazone (IBT) exhibits significant intercalation into calf thymus DNA (CT-DNA).
  • The binding process is primarily driven by enthalpy, suggesting favorable interactions within the DNA structure.
  • These findings provide insights into the molecular basis of IBT-DNA interactions, relevant for medicinal chemistry applications.

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