Integration and global analysis of isothermal titration calorimetry data for studying macromolecular interactions

被引:199
作者
Brautigam, Chad A. [1 ]
Zhao, Huaying [2 ]
Vargas, Carolyn [3 ]
Keller, Sandro [3 ]
Schuck, Peter [2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Biophys, Dallas, TX 75390 USA
[2] Natl Inst Biomed Imaging & Bioengn, Dynam Macromol Assembly Sect, Lab Cellular Imaging & Macromol Biophys, NIH, Bethesda, MD USA
[3] Univ Kaiserslautern, Mol Biophys, D-67663 Kaiserslautern, Germany
基金
美国国家卫生研究院;
关键词
HIGH-AFFINITY BINDING; MULTIMETHOD ANALYSIS; SIGNALING COMPLEXES; THERMODYNAMICS; RECOGNITION; CONSTANTS; SYSTEMS; ITC; QUANTIFICATION; COOPERATIVITY;
D O I
10.1038/nprot.2016.044
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Isothermal titration calorimetry (ITCTC) is a powerful and widely used method to measure the energetics of macromolecular interactions by recording a thermogram of differential heating power during a titration. However, traditional ITCTC analysis is limited by stochastic thermogram noise and by the limited information content of a single titration experiment. Here we present a protocol for bias-free thermogram integration based on automated shape analysis of the injection peaks, followed by combination of isotherms from different calorimetric titration experiments into a global analysis, statistical analysis of binding parameters and graphical presentation of the results. This is performed using the integrated public-domain software packages NITPTPIC, SESEDPHATAT and GUSSUSSUSSI. The recently developed low-noise thermogram integration approach and global analysis allow for more precise parameter estimates and more reliable quantification of multisite and multicomponent cooperative and competitive interactions. Titration experiments typically take 1-2.5 h each, and global analysis usually takes 10-20 min.
引用
收藏
页码:882 / 894
页数:13
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