3, 5-Dihydroxy 4', 7-dimethoxyflavone-DNA interaction study for nucleic acid detection and differential cell staining

Int J Biol Macromol. 2024 Mar;261(Pt 1):129713. doi: 10.1016/j.ijbiomac.2024.129713. Epub 2024 Jan 26.

Abstract

The present study is focused on application of a natural compound, 3, 5-dihydroxy 4', 7-dimethoxyflavone (DHDM) from a medicinal plant Alpinia nigra for nucleic acid detection and differential cell staining. DHDM was found to interact with nucleic acid and forms complex, which was investigated for various applications. It was successfully utilized to visualize plasmid, genomic, and ds-linear DNA in agarose gel electrophoresis without affecting the DNA mobility in the gel. Fluorescence of DHDM increased several fold upon binding to dsDNA. Photostability of the compound was assessed and showed photobleaching effect that decreased gradually over time. Application of the compound was further extended to differential cell staining. When observed in fluorescence microscope, DHDM stained the dead cells and differentiated them from live cells in the case of bacterial, yeast, and mammalian cells. Higher concentration of the compound was found to be less cytotoxic to cancerous cells. Nucleic acid staining dyes like Ethidium bromide (EtBr), Propidium iodide (PI), etc. are carcinogens and environmental pollutants and therefore DHDM a natural compound, is a major benefit and thus can serve as an alternative to the current dyes.

Keywords: Agarose gel electrophoresis; Cell staining; Fluorescence microscopy; Natural product; Nucleic acid.

MeSH terms

  • Animals
  • Coloring Agents / chemistry
  • DNA* / metabolism
  • Electrophoresis, Agar Gel
  • Ethidium
  • Mammals / metabolism
  • Nucleic Acids*
  • Staining and Labeling

Substances

  • DNA
  • Ethidium
  • Coloring Agents
  • Nucleic Acids