Isothermal titration calorimetry of membrane proteins - Progress and challenges

被引:81
|
作者
Rajarathnam, Krishna [1 ,2 ]
Roesgen, Joerg [3 ]
机构
[1] Univ Texas Med Branch, Dept Biochem & Mol Biol, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Sealy Ctr Struct Biol & Mol Biophys, Galveston, TX 77555 USA
[3] Penn State Coll Med, Dept Biochem & Mol Biol, Hershey, PA 17033 USA
来源
基金
美国国家卫生研究院;
关键词
Isothermal titration calorimetry (ITC); Membrane proteins; Thermodynamics; Enthalpy; Affinity; Drug discovery; LIGAND-BINDING; METAL-BINDING; RECEPTOR; THERMODYNAMICS; INTERLEUKIN-8; DISSOCIATION; RECOGNITION; COMPLEX; CXCR1; DIMER;
D O I
10.1016/j.bbamem.2013.05.023
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
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.
引用
收藏
页码:69 / 77
页数:9
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