Literature DB >> 16257377

Measurements of binding thermodynamics in drug discovery.

Geoffrey A Holdgate1, Walter H J Ward.   

Abstract

Thermodynamics governs the process of biomolecular recognition. The steps of characterizing, understanding and exploiting binding thermodynamics have the potential to contribute to an improved rational drug design process that is more robust and reliable. It is only relatively recently that instrumentation capable of direct and full thermodynamic characterization has been improved, giving impetus to the application of thermodynamic measurements in drug discovery. This review highlights current instruments and methods that can be employed to measure binding thermodynamics and their use in studies of biomolecular recognition and drug discovery.

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Year:  2005        PMID: 16257377     DOI: 10.1016/S1359-6446(05)03610-X

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  32 in total

1.  Studying multisite binary and ternary protein interactions by global analysis of isothermal titration calorimetry data in SEDPHAT: application to adaptor protein complexes in cell signaling.

Authors:  Jon C D Houtman; Patrick H Brown; Brent Bowden; Hiroshi Yamaguchi; Ettore Appella; Lawrence E Samelson; Peter Schuck
Journal:  Protein Sci       Date:  2007-01       Impact factor: 6.725

2.  Data quality in drug discovery: the role of analytical performance in ligand binding assays.

Authors:  Hermann Wätzig; Imke Oltmann-Norden; Franziska Steinicke; Hassan A Alhazmi; Markus Nachbar; Deia Abd El-Hady; Hassan M Albishri; Knut Baumann; Thomas Exner; Frank M Böckler; Sami El Deeb
Journal:  J Comput Aided Mol Des       Date:  2015-06-13       Impact factor: 3.686

Review 3.  Cellular analysis of the action of epigenetic drugs and probes.

Authors:  Mirjam Hau; Fides Zenk; A Ganesan; Nicola Iovino; Manfred Jung
Journal:  Epigenetics       Date:  2017-01-10       Impact factor: 4.528

4.  Measuring Biomolecular DSC Profiles with Thermolabile Ligands to Rapidly Characterize Folding and Binding Interactions.

Authors:  Robert W Harkness V; Philip E Johnson; Anthony K Mittermaier
Journal:  J Vis Exp       Date:  2017-11-21       Impact factor: 1.355

5.  Characterization of interaction between amino acids and fulvic-like organic matter by fluorescence spectroscopy combining thermodynamic calculation.

Authors:  Tao Lin; Bingwei Hou; Jian Wang; Yaqun Xu; Wei Chen
Journal:  Environ Sci Pollut Res Int       Date:  2017-01-18       Impact factor: 4.223

Review 6.  Thermodynamic studies for drug design and screening.

Authors:  Nichola C Garbett; Jonathan B Chaires
Journal:  Expert Opin Drug Discov       Date:  2012-03-08       Impact factor: 6.098

Review 7.  Expanding the number of 'druggable' targets: non-enzymes and protein-protein interactions.

Authors:  Leah N Makley; Jason E Gestwicki
Journal:  Chem Biol Drug Des       Date:  2013-01       Impact factor: 2.817

Review 8.  Fragment-based approaches to enzyme inhibition.

Authors:  Alessio Ciulli; Chris Abell
Journal:  Curr Opin Biotechnol       Date:  2007-10-24       Impact factor: 9.740

Review 9.  Biophysical characterization of recombinant proteins: a key to higher structural genomics success.

Authors:  Masoud Vedadi; Cheryl H Arrowsmith; Abdellah Allali-Hassani; Guillermo Senisterra; Gregory A Wasney
Journal:  J Struct Biol       Date:  2010-05-11       Impact factor: 2.867

10.  A microfabricated nanocalorimeter: design, characterization, and chemical calibration.

Authors:  Junkai Xu; Ron Reiserer; Joel Tellinghuisen; John P Wikswo; Franz J Baudenbacher
Journal:  Anal Chem       Date:  2008-03-20       Impact factor: 6.986

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