Molnupiravir's Electrochemical Behavior and Binding Interactions with Biomolecules Studied in New Research
Recent research from Anurag University has investigated the electrochemical behavior and binding interactions of the antiviral drug Molnupiravir (MPV) with key biomolecules. The study, published in the journal Biochemical and Biophysical Research Communications, employed cyclic voltammetry (CV) and molecular dynamics (MD) simulations to examine MPV's interactions with bovine serum albumin (BSA) and ctDNA.
Key Takeaways:
- The research found that MPV exhibits an irreversible anodic peak at a peak potential of +0.860 V on the glassy carbon electrode (GCE) at pH 7.0.
- The study demonstrated a linear concentration range of 35 mM-200 mM for MPV, suggesting a good analytical approach for its quantification in real samples.
- The in vitro binding studies with ctDNA and BSA using CV indicated a reduction in peak current and positive potential shift, suggesting an intercalative or groove-binding interaction mode.
- MD simulations confirmed the stability of MPV-DNA and MPV-BSA complexes, stabilized mainly by van der Waals forces with additional contributions from hydrogen bonding and electrostatic interactions.
- The study revealed that MPV's affinity for BSA could enhance its pharmacokinetic profile through binding and transport within serum proteins.
- The results demonstrated a higher binding affinity of MPV with ctDNA and BSA, highlighting the need for genotoxicity assessment.
Statistics:
- The pH levels used in the study were 4.0, 7.0, and 9.2.
- The concentration range of MPV was 35 mM-200 mM.
- The peak potential of MPV on the GCE was +0.860 V at pH 7.0.
- The peak current of MPV reduction was observed to be decreased with the increase in ctDNA concentration.
- The binding affinity of MPV with BSA was found to be higher compared to ctDNA.
Sources:
- Electrochemical interpretations for the study of molnupiravir binding interactions with bovine serum albumin and DNA and molecular dynamics studies. Biochemical and Biophysical Research Communications, 2025;769:151988.