Literature DB >> 34549492

An "Onion-like" Model of Protein Unfolding: Collective versus Site Specific Approaches.

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.
© 2021 Wiley-VCH GmbH.

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


  1 in total

1.  Monitoring protein unfolding transitions by NMR-spectroscopy.

Authors:  Matthias Dreydoppel; Jochen Balbach; Ulrich Weininger
Journal:  J Biomol NMR       Date:  2022-01-04       Impact factor: 2.582

  1 in total

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