Penkov, Nikita, Valery Yashin, Eugeny Fesenko Jr, Andrew Manokhin, and Eugeny Fesenko. "A Study of the Effect of a Protein on the Structure of Water in Solution Using Terahertz Time-Domain Spectroscopy." Applied Spectroscopy (2017): 0003702817735551.
Abstract
Terahertz time-domain spectroscopy (THz-TDS) was used to determine the spectra (range ¼ 1.2–120 cm-1
) of aqueous
solutions of bovine serum albumin (BSA) at pH range 2.5–10. Under each of the selected pH, BSA molecules exist in a
different conformation, compared to other pH values. The spectra were used to calculate the functions of the dielectric
permittivity of BSA solutions. Dielectric functions of the aqueous phase of BSA solutions were calculated based on the
Bruggeman model, without the contribution of BSA itself. Fitting of the dielectric functions was performed using a model
which includes three water spectral bands: two relaxation bands with relaxation times of about 8.28 and 0.3 ps and a
vibrational band with a maximum of about 180 cm-1
. The parameters of these bands were determined through fitting and
physical interpretation at the molecular level can be provided for each of them. A comparison between the values of model
parameters of solutions with BSA and without BSA allowed to conclude that the main effect of BSA is the formation of
strongly bound hydration shells in the immediate proximity to the protein molecule. At the same time, the structure of more
distant layers of the hydration shells is destroyed, with an increased formation of free water molecules. Some differences are
observed in the effect of different BSA conformations on the aqueous phase of solution. The proposed approach can be
generalized and applied for studying of a wide class of biological macromolecules in aqueous solutions.
… by the spectral properties of the solvent water. The fact is that the absorption coefficient of … TPS Spectra 3000 spectrometer (Teraview, UK) in the wave number range from 1.2 to 120 … of electric field into the spectra was performed using the Blackman–Harris 3 apodization function …
for full paper see http://journals.sagepub.com/doi/pdf/10.1177/0003702817735551
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