Biophysical approaches for the study of metal-protein interactions

被引:20
|
作者
Witkowska, Danuta [1 ]
Rowinska-Zyrek, Magdalena [2 ]
机构
[1] Publ Higher Med Profess Sch Opole, Katowicka 68, PL-45060 Opole, Poland
[2] Univ Wroclaw, Fac Chem, F Joliot Curie 14, PL-50383 Wroclaw, Poland
关键词
Metal-protein interactions; Analytical techniques; Biophysical methods; Structural and kinetic tools; ISOTHERMAL TITRATION CALORIMETRY; SURFACE-PLASMON RESONANCE; RAY-ABSORPTION SPECTROSCOPY; CIRCULAR-DICHROISM SPECTRA; HIGH-AFFINITY BINDING; EF-HAND PROTEINS; LA-ICP-MS; MASS-SPECTROMETRY; BIOLOGICAL MACROMOLECULES; EPR SPECTROSCOPY;
D O I
10.1016/j.jinorgbio.2019.110783
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protein-protein interactions play important roles for a variety of cell functions, often involving metal ions; in fact, metal-ion binding mediates and regulates the activity of a wide range of biomolecules. Enlightening all of the specific features of metal-protein and metal-mediated protein-protein interactions can be a very challenging task; a detailed knowledge of the thermodynamic and spectroscopic parameters and the structural changes of the protein is normally required. For this purpose, many experimental techniques are employed, embracing all fields of Analytical and Bioinorganic Chemistry. In addition, the use of peptide models, reproducing the primary sequence of the metal-binding sites, is also proved to be useful. In this paper, a review of the most useful techniques for studying ligand-protein interactions with a special emphasis on metal-protein interactions is provided, with a critical summary of their strengths and limitations.
引用
收藏
页数:10
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