Simultaneous determination of thermodynamic and kinetic data by isothermal titration calorimetry

被引:6
作者
Gloeckner, Steffen [1 ]
Klebe, Gerhard [1 ]
机构
[1] Philipps Univ Marburg, Inst Pharmaceut Chem, Marbacher Weg 6, D-35037 Marburg, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2021年 / 1865卷 / 02期
关键词
Thermodynamic binding data; Kinetic binding data; Measurement protocol; kinITC; 1:1 protein-ligand complexes; Drug optimization; BINDING THERMODYNAMICS; CARBONIC-ANHYDRASE; CONSTANTS; PROFILES; AFFINITY; KINITC; ITC;
D O I
10.1016/j.bbagen.2020.129772
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: Thermodynamic and binding kinetic data increasingly support and guide the drug optimization process. Methods: Because ITC thermograms contain binding thermodynamic and kinetic information, an efficient protocol for the simultaneous extraction of thermodynamic and kinetic data for 1:1 protein ligand reactions from AFFINImeter kinITC in one single experiment are presented. Results: The effort to apply this protocol requires the same time as for the standard protocol but increases the precision of both thermodynamic and kinetic data. Conclusions: The protocol enables reliable extraction of both thermodynamic and kinetic data for 1:1 protein-ligand binding reactions with improved precision compared to the 'standard protocol'. General significance: Thermodynamic and kinetic data are recorded under exactly the same conditions in solution without any labeling or immobilization from a protein sample that is not 100% active and would otherwise render the extraction of kinetic parameters impossible.
引用
收藏
页数:7
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