Abstract

Protein ligand interactions play an important role in biology. Increasingly the aim is to understand and influence protein ligand binding. The binding process is heavily influenced by its thermodynamic parameters. In order to understand how the whole system thermodynamics work it is important to characterise the individual contribution of each of the systems components. While the change in conformational entropy of the protein can be determined using QENS complementary methods are necessary in order to characterise all components. This paper will describe the challenges that can occur when combining the different methods, as well as how they can be overcome.

Details

Title
Complementary approaches to obtaining thermodynamic parameters from protein ligand systems-challenges and opportunities
Author
Sarter, Mona; Niether, Doreen; Wiegand, Simone; Fitter, Joerg; Stadler, Andreas M
Section
QENS
Publication year
2022
Publication date
2022
Publisher
EDP Sciences
ISSN
21016275
e-ISSN
2100014X
Source type
Conference Paper
Language of publication
English
ProQuest document ID
3192939716
Copyright
© 2022. This work is licensed under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and conditions, you may use this content in accordance with the terms of the License.