Literature DB >> 26328629

Biophysical approaches for the study of interactions between molecular chaperones and protein aggregates.

Maya A Wright1, Francesco A Aprile, Paolo Arosio, Michele Vendruscolo, Christopher M Dobson, Tuomas P J Knowles.   

Abstract

Molecular chaperones are key components of the arsenal of cellular defence mechanisms active against protein aggregation. In addition to their established role in assisting protein folding, increasing evidence indicates that molecular chaperones are able to protect against a range of potentially damaging aspects of protein behaviour, including misfolding and aggregation events that can result in the generation of aberrant protein assemblies whose formation is implicated in the onset and progression of neurodegenerative disorders such as Alzheimer's and Parkinson's diseases. The interactions between molecular chaperones and different amyloidogenic protein species are difficult to study owing to the inherent heterogeneity of the aggregation process as well as the dynamic nature of molecular chaperones under physiological conditions. As a consequence, understanding the detailed microscopic mechanisms underlying the nature and means of inhibition of aggregate formation remains challenging yet is a key objective for protein biophysics. In this review, we discuss recent results from biophysical studies on the interactions between molecular chaperones and protein aggregates. In particular, we focus on the insights gained from current experimental techniques into the dynamics of the oligomerisation process of molecular chaperones, and highlight the opportunities that future biophysical approaches have in advancing our understanding of the great variety of biological functions of this important class of proteins.

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Year:  2015        PMID: 26328629     DOI: 10.1039/c5cc03689e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  The binding of the small heat-shock protein αB-crystallin to fibrils of α-synuclein is driven by entropic forces.

Authors:  Tom Scheidt; Jacqueline A Carozza; Carl C Kolbe; Francesco A Aprile; Olga Tkachenko; Mathias M J Bellaiche; Georg Meisl; Quentin A E Peter; Therese W Herling; Samuel Ness; Marta Castellana-Cruz; Justin L P Benesch; Michele Vendruscolo; Christopher M Dobson; Paolo Arosio; Tuomas P J Knowles
Journal:  Proc Natl Acad Sci U S A       Date:  2021-09-21       Impact factor: 12.779

2.  Defining Hsp33's Redox-regulated Chaperone Activity and Mapping Conformational Changes on Hsp33 Using Hydrogen-deuterium Exchange Mass Spectrometry.

Authors:  Rosi Fassler; Nufar Edinger; Oded Rimon; Dana Reichmann
Journal:  J Vis Exp       Date:  2018-06-07       Impact factor: 1.355

3.  Cooperative Assembly of Hsp70 Subdomain Clusters.

Authors:  Maya A Wright; Francesco A Aprile; Mathias M J Bellaiche; Thomas C T Michaels; Thomas Müller; Paolo Arosio; Michele Vendruscolo; Christopher M Dobson; Tuomas P J Knowles
Journal:  Biochemistry       Date:  2018-05-29       Impact factor: 3.162

  3 in total

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