| Literature DB >> 34549492 |
Anastasia S Politou1,2, Annalisa Pastore3, Piero Andrea Temussi3.
Abstract
Approximating protein unfolding by an all-or-none cooperative event is a convenient assumption that can provide precious global information on protein stability. It is however quickly emerging that the scenario is far more complex and that global denaturation curves often hide a rich heterogeneity of states that are largely probe dependent. In this review, we revisit the importance of gaining site-specific information on the unfolding process. We focus on nuclear magnetic resonance, as this is the main technique able to provide site-specific information. We review historical and most modern approaches that have allowed an appreciable advancement of the field of protein folding. We also demonstrate how unfolding is a reporter dependent event, suggesting the outmost importance of selecting the reporter carefully.Entities:
Keywords: NMR; fluorescence; protein stability; thermal unfolding; thermodynamics
Mesh:
Year: 2021 PMID: 34549492 DOI: 10.1002/cphc.202100520
Source DB: PubMed Journal: Chemphyschem ISSN: 1439-4235 Impact factor: 3.102