Phase separation, aggregation, and complexation of triton-X100 and bovine serum albumin mixture: A combined cloud point and UV-visible spectroscopic approaches

Int J Biol Macromol. 2024 Jun;269(Pt 2):132184. doi: 10.1016/j.ijbiomac.2024.132184. Epub 2024 May 7.

Abstract

Phase separation and aggregation behaviour of triton X-100 (TX-100) and bovine serum albumin (BSA) mixture were investigated using cloud point and UV-visible spectroscopic techniques. The effects of various hydrotropes (HYTs) - namely, sodium salicylate (SS), sodium benzoate (SB), glycerol (Glyc), and 4-aminobenzoic acid (4-ABA) - on the cloud point (CP) of TX-100 + BSA were determined. The obtained CP values for the mixed system in the presence of HYTs followed the order: The measured critical micellization concentration (CMC) values of the TX-100 + BSA mixture were found to be significantly altered with varying amounts of BSA. The calculated free energy of clouding and micellization indicated the non-spontaneous nature of the phase transition and the spontaneous association of the TX-100 + BSA mixture. The non-spontaneity of phase separation decreased with increasing concentrations of HYTs. The enumerated values of ∆Hco and ∆Sco were consistently recorded as negative and positive magnitudes, respectively, in all aqueous HYTs media. The clouding process occurred due to a combination of hydrophobic and electrostatic interactions. The binding constant of the mixed system was determined employing the UV-vis spectroscopic method using the Benesi-Hildebrand equation.

Keywords: Interaction; Protein BSA; Thermodynamic.

MeSH terms

  • Animals
  • Cattle
  • Hydrophobic and Hydrophilic Interactions
  • Micelles
  • Octoxynol* / chemistry
  • Phase Separation
  • Phase Transition
  • Protein Aggregates
  • Serum Albumin, Bovine* / chemistry
  • Spectrophotometry, Ultraviolet*
  • Surface-Active Agents / chemistry

Substances

  • Serum Albumin, Bovine
  • Octoxynol
  • Protein Aggregates
  • Micelles
  • Surface-Active Agents