Exploring the binding mechanisms of inorganic magnetic nanocarrier containing L-Dopa with HSA protein utilizing multi spectroscopic techniques

J Biomol Struct Dyn. 2021 Nov;39(18):7160-7167. doi: 10.1080/07391102.2020.1806929. Epub 2020 Aug 14.

Abstract

In this study, the interaction of Fe3O4@CaAl-LDH@L-Dopa nanoparticles (NPs) with human serum albumin (HSA) was investigated in simulated physiological conditions applying UV-visible, fluorescence, and circular dichroism (CD) spectroscopic techniques. The consequences of UV-vis and CD spectroscopy demonstrated that the interaction of HSA to Fe3O4@CaAl-LDH@L-Dopa NPs enforced some conformational alterations within HSA. The fluorescence spectroscopy analysis indicated that by enhancing temperature, the Stern-Volmer quenching constant (Ksv) was decreased, which is relevant to a static quenching mechanism. The binding constant (Kb) was 7.07 × 104M-1 while the number of the binding site (n) was 0.94 which is in compromise with its binding constant. Also, thermodynamic parameters (ΔH° > 0, ΔG° < 0, and ΔS° > 0) have suggested that hydrophobic forces perform a key role in the interaction of HSA with Fe3O4@CaAl-LDH@L-Dopa NPs. Displacement studies successfully carried out using the Warfarin and Ibuprofen have predicted that the binding of Fe3O4@CaAl-LDH@L-Dopa NPs to HSA is situated at site II (subdomain IIIA).Communicated by Ramaswamy H. Sarma.

Keywords: HSA; L-Dopa; Multi spectroscopy; binding constant.

MeSH terms

  • Binding Sites
  • Circular Dichroism
  • Humans
  • Levodopa*
  • Magnetic Phenomena
  • Molecular Docking Simulation
  • Protein Binding
  • Serum Albumin, Human* / metabolism
  • Spectrometry, Fluorescence
  • Thermodynamics

Substances

  • Levodopa
  • Serum Albumin, Human