Analysis of the Hydration Water around Bovine Serum Albumin Using Terahertz Coherent Synchrotron Radiation

被引:83
作者
Bye, Jordan W. [1 ]
Meliga, Stefano [2 ]
Ferachou, Denis [3 ]
Cinque, Gianfelice [4 ]
Zeitler, J. Axel [3 ]
Falconer, Robert J. [1 ]
机构
[1] Univ Sheffield, Dept Chem & Biol Engn, ChELSI Inst, Sheffield S1 3JD, S Yorkshire, England
[2] Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
[3] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge CB2 3RA, England
[4] Diamond Light Source, Didcot OX11 0QX, Oxon, England
基金
英国工程与自然科学研究理事会;
关键词
THZ ABSORPTION-SPECTROSCOPY; FAR-INFRARED SPECTROSCOPY; MOLECULAR-DYNAMICS; HOFMEISTER SERIES; PROTEIN; SHELL; STABILITY; PEPTIDES;
D O I
10.1021/jp407410g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Terahertz spectroscopy was used to study the absorption of bovine serum albumin (BSA) in water. The Diamond Light Source operating in a low alpha mode generated coherent synchrotron radiation that covered a useable spectral bandwidth of 0.3-3.3 THz (10-110 cm(-1)). As the BSA concentration was raised, there was a nonlinear change in absorption inconsistent with Beer's law. At low BSA concentrations (0-1 mM), the absorption remained constant or rose slightly. Above a concentration of 1 mM BSA, a steady decrease in absorption was observed, which was followed by a plateau that started at 2.5 mM. Using a overlapping hydration layer model, the hydration layer was estimated to extend 15 A from the protein. Calculation of the corrected absorption coefficient (alpha(corr)) for the water around BSA by subtracting the excluded volume of the protein provides an alternative approach to studying the hydration layer that provides evidence for complexity in the population of water around BSA.
引用
收藏
页码:83 / 88
页数:6
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