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
相关论文
共 60 条
[1]  
[Anonymous], 2004, CURR PROTOC CELL BIO
[2]   A comprehensive calorimetric investigation of an entropically driven T cell receptor-peptide/major histocompatibility complex interaction [J].
Armstrong, Kathryn M. ;
Baker, Brian M. .
BIOPHYSICAL JOURNAL, 2007, 93 (02) :597-609
[3]   CALORIMETRIC DETERMINATION OF COOPERATIVE INTERACTIONS IN HIGH-AFFINITY BINDING PROCESSES [J].
BAINS, G ;
FREIRE, E .
ANALYTICAL BIOCHEMISTRY, 1991, 192 (01) :203-206
[4]   Evaluation of linked protonation effects in protein binding reactions using isothermal titration calorimetry [J].
Baker, BM ;
Murphy, KP .
BIOPHYSICAL JOURNAL, 1996, 71 (04) :2049-2055
[5]   Intrinsic thermodynamics of ethoxzolamide inhibitor binding to human carbonic anhydrase XIII [J].
Baranauskiene, Lina ;
Matulis, Daumantas .
BMC BIOPHYSICS, 2012, 5
[6]  
Bevington P. R., 2002, Data reduction and error analysis for the physical sciences
[7]   Calculations and Publication-Quality Illustrations for Analytical Ultracentrifugation Data [J].
Brautigam, Chad A. .
ANALYTICAL ULTRACENTRIFUGATION, 2015, 562 :109-133
[8]   Fitting two- and three-site binding models to isothermal titration calorimetric data [J].
Brautigam, Chad A. .
METHODS, 2015, 76 :124-136
[9]   Revisiting the optimal c value for isothermal titration calorimetry [J].
Broecker, Jana ;
Vargas, Carolyn ;
Keller, Sandro .
ANALYTICAL BIOCHEMISTRY, 2011, 418 (02) :307-309
[10]   Analysis of Cooperativity by Isothermal Titration Calorimetry [J].
Brown, Alan .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2009, 10 (08) :3457-3477