Integral membrane proteins, including G protein-coupled receptors (GPCR) and ion channels, mediate diverse biological functions that are crucial to all aspects of life. The knowledge of the molecular mechanisms, and in particular, the thermodynamic basis of the binding interactions of the extracellular ligands and intracellular effector proteins is essential to understand the workings of these remarkable nanomachines. In this review, we describe how isothermal titration calorimetry (ITC) can be effectively used to gain valuable insights into the thermodynamic signatures (enthalpy, entropy, affinity, and stoichiometry), which would be most useful for drug discovery studies, considering that more than 30% of the current drugs target membrane proteins. This article is part of a Special Issue entitled: Structural and biophysical characterisation of membrane protein-ligand binding. (C) 2013 Elsevier B.V. All rights reserved.
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Vilnius Univ, Inst Biotechnol, Life Sci Ctr, Dept Biothermodynam & Drug Design, Sauletekio 7, LT-10257 Vilnius, LithuaniaVilnius Univ, Inst Biotechnol, Life Sci Ctr, Dept Biothermodynam & Drug Design, Sauletekio 7, LT-10257 Vilnius, Lithuania
Baranauskiene, Lina
Kuo, Tai-Chih
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Taipei Med Univ, Dept Biochem, Taipei, TaiwanVilnius Univ, Inst Biotechnol, Life Sci Ctr, Dept Biothermodynam & Drug Design, Sauletekio 7, LT-10257 Vilnius, Lithuania
Kuo, Tai-Chih
Chen, Wen-Yih
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Natl Cent Univ, Dept Chem & Mat Engn, Taoyuan, TaiwanVilnius Univ, Inst Biotechnol, Life Sci Ctr, Dept Biothermodynam & Drug Design, Sauletekio 7, LT-10257 Vilnius, Lithuania