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Facile Preparation of Internally Self-assembled Lipid Particles Stabilized by Carbon Nanotubes
Published on: February 19, 2016
Influence of Bovine Liver Catalase on Self-Assembled Structures of a Surface-Active Ionic Liquid
Sudhanshu Sharma1, Dineshbabu Takkella1, Jyoti Vishwakarma1
1Department of Chemistry, Indian Institute of Technology Hyderabad, Kandi, Sangareddy 502284, Telangana, India.
Abstract:
The modulation of self-assembled structures of a surface-active ionic liquid (SAIL), 1-butyl-3-methylimidazolium octyl sulfate [C4mim][C8OSO3], upon their interaction with bovine liver catalase (CAT) enzyme is investigated in this study. The intrinsic fluorescence of tryptophan (Trp) was investigated to monitor the conformational changes in CAT with [C4mim][C8OSO3]. Extrinsic fluorescence of the 8-anilino-1-naphthalenesulfonic acid (ANS) probe was further utilized to determine the structural and conformational changes along with the binding location of [C4mim][C8OSO3] in the enzyme. Fourier transform infrared (FTIR) measurements quantify the secondary structure changes, leading to modulation in the fluorescence characteristics. To elucidate modulation of the self-assembled structures, fluorescence lifetime imaging microscopy (FLIM) measurements were utilized. On adding CAT to an aqueous micellar solution of [C4mim][C8OSO3], there was the appearance of highly fluorescent ring-like structures. The internal structure of these was further investigated using transmission electron microscopy (TEM), where the ring sizes were found to be dependent upon the quantity of enzyme taken. These structures completely collapse and accumulate when the CAT concentration reaches near ∼5-7 μM. Further, the activity of the CAT enzyme was assessed in the presence of [C4mim][C8OSO3] depending upon the premicelle and micelle self-assemblies. Molecular dynamics (MD) simulation study was used to further analyze the binding location of the micelle-forming entity, [C8OSO3], and it was found that the [C8OSO3] species tends to remain at the enzyme active site. The results describe the unique transformation in self-assemblies of a SAIL by enzymatic action that has not been studied so far and opens up the interesting applications of SAIL in biomedical applications.

