等温滴定量热法
化学
量热法
滴定法
血浆蛋白结合
质子化
能量学
结合蛋白
结合位点
生物化学
脱质子化
配体(生物化学)
生物物理学
结晶学
生物
物理化学
有机化学
热力学
物理
离子
基因
受体
生态学
作者
Adrián Velázquez‐Campoy,Hiroyasu Ohtaka,Azin Nezami,Salman Muzammil,Ernesto Freire
标识
DOI:10.1002/0471143030.cb1708s23
摘要
In the last two decades, isothermal titration calorimetry (ITC) has become the preferred technique to determine the binding energetics of biological processes, including protein-ligand binding, protein-protein binding, DNA-protein binding, protein-carbohydrate binding, protein-lipid binding, and antigen-antibody binding. In this unit several protocols are presented, ranging from the basic ones that are aimed at characterizing binding of moderate affinity to advanced protocols that are aimed at determining very high or very low affinity binding processes. Also, alternate protocols for special cases (homodimeric proteins and unstable proteins) and additional information accessible by ITC (heat capacity and protonation/deprotonation processes coupled to binding) are presented.
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