Understanding the binding behavior of Malathion with calf thymus DNA by spectroscopic, cell viability and molecular dynamics simulation techniques: binary and ternary systems comparison

Abstract

The interaction between calf thymus DNA (ctDNA) and Malathion in the absence and presence of Histone 1 has been enquired by the means of spectroscopic, viscometry, molecular modeling, and cell viability assay techniques. Malathion is capable of quenching the fluorescence of ct DNA in the absence and presence of H1. The binding constants of Malathion–ctDNA complex in the absence of H1 have been calculated to be 6.62 × 10⁴, 4.31 × 10⁴ and 1.93 × 10⁴ M⁻¹ at 298, 303, and 308 K, respectively that revealed static quenching in complex formation. The observed negative values of enthalpy and entropy changes indicate that the main binding interaction forces were van der Waals force and hydrogen bonding. The binding constant between Malathion and single-stranded ctDNA (ss ctDNA) seemed to be much weaker than that of Malathion and double-stranded ctDNA (ds ctDNA). Furthermore, Malathion can induce detectable alterations in the CD spectrum of ctDNA, along with changes in its viscosity. In the presence of H1, fluorescence quenching of ctDNA–Malathion complex displays dynamic behavior and binding constants were perceived to be 1.66 × 10⁴, 2.93 × 10⁴ and 5.77 × 10⁴ M⁻¹ at 298, 303, and 308 K, respectively. The different of interaction behavior between ctDNA and Malathion in the absence and presence of H1 clearly revealed H1 role in the complex formation and forces change between ctDNA and Malathion. The positive values of enthalpy and entropy changes have suggested that binding process is primarily driven by hydrophobic interactions. The tendency to interact with ss ctDNA, reduced viscosity have designated that the Malathion bound to ctDNA in the presence of H1 is groove binding. The results of molecular docking and molecular dynamics simulation also confirmed potent interactions between Malathion and the macromolecules in the binary and ternary systems.

Communicated by Ramaswamy H. Sarma

Keywords:

• Malathion
• H1
• spectroscopic techniques
• molecular modeling
• MTT assay

Acknowledgments

The financial support of the Research Council of the Islamic Azad University, Mashhad Branch and Mashhad University of Medical Sciences are gratefully acknowledged. The authors thank Dr. Ljungburg for English editing.

Disclosure statement

The authors declare no conflict of interest in regard to this article.

Additional information

Funding

The financial support of the Research Council of the Mashhad Branch, Islamic Azad University and Mashhad University of Medical Sciences are appreciated and acknowledged.