On the link between conformational changes, ligand binding and heat capacity

被引:52
|
作者
Vega, S. [1 ]
Abian, O. [1 ,3 ,4 ,5 ]
Velazquez-Campoy, A. [1 ,2 ,3 ,6 ]
机构
[1] Univ Zaragoza, Joint Unit IQFR CSIC BIFI, Inst Biocomputat & Phys Complex Syst BIFI, Zaragoza, Spain
[2] Univ Zaragoza, Dept Biochem & Mol & Cell Biol, Zaragoza, Spain
[3] IIS Aragon, Zaragoza, Spain
[4] Inst Aragones Ciencias Salud, Zaragoza, Spain
[5] Ctr Invest Biomed Red Area Temat Enfermedades Hep, Aragon, Spain
[6] Govt Aragon, Fdn ARAID, Aragon, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2016年 / 1860卷 / 05期
关键词
Ligand binding; Conformational change; Allostery; Heat capacity change; Isothermal titration calorimetry; Conformational selection and induced fit; INDUCED-FIT; POPULATION-SHIFT; PROTEIN-BINDING; THERMODYNAMICS; SELECTION; ENERGETICS; RECOGNITION; STABILITY; MECHANISM; NUCLEOTIDES;
D O I
10.1016/j.bbagen.2015.10.010
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
Background: Conformational changes coupled to ligand binding constitute the structural and energetics basis underlying cooperativity, allostery and, in general, protein regulation. These conformational rearrangements are associated with heat capacity changes. ITC is a unique technique for studying binding interactions because of the simultaneous determination of the binding affinity and enthalpy, and for providing the best estimates of binding heat capacity changes. Scope of review: Still controversial issues in ligand binding are the discrimination between the "conformational selection model" and the "induced fit model", and whether or not conformational changes lead to temperature dependent apparent binding heat capacities. The assessment of conformational changes associated with ligand binding by ITC is discussed. In addition, the "conformational selection" and "induced fit" models are reconciled, and discussed within the context of intrinsically (partially) unstructured proteins. Major conclusions: Conformational equilibrium is a major contribution to binding heat capacity changes. A simple model may explain both conformational selection and induced fit scenarios. A temperature-independent binding heat capacity does not necessarily indicate absence of conformational changes upon ligand binding. ITC provides information on the energetics of conformational changes associated with ligand binding (and other possible additional coupled equilibria). General significance: Preferential ligand binding to certain protein states leads to an equilibrium shift that is reflected in the coupling between ligand binding and additional equilibria. This represents the structural/energetic basis of the widespread dependence of ligand binding parameters on temperature, as well as pH, ionic strength and the concentration of other chemical species. This article is part of a Special Issue entitled Microcalorimetry in the BioSciences - Principles and Applications, edited by Fadi Bou-Abdallah. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:868 / 878
页数:11
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