Literature DB >> 25194824

Antibodies and protein misfolding: From structural research tools to therapeutic strategies.

Erwin De Genst1, Anne Messer2, Christopher M Dobson3.   

Abstract

Protein misfolding disorders, including the neurodegenerative conditions Alzheimer's disease (AD) and Parkinson's disease (PD) represent one of the major medical challenges or our time. The underlying molecular mechanisms that govern protein misfolding and its links with disease are very complex processes, involving the formation of transiently populated but highly toxic molecular species within the crowded environment of the cell and tissue. Nevertheless, much progress has been made in understanding these events in recent years through innovative experiments and therapeutic strategies, and in this review we present an overview of the key roles of antibodies and antibody fragments in these endeavors. We discuss in particular how these species are being used in combination with a variety of powerful biochemical and biophysical methodologies, including a range of spectroscopic and microscopic techniques applied not just in vitro but also in situ and in vivo, both to gain a better understanding of the mechanistic nature of protein misfolding and aggregation and also to design novel therapeutic strategies to combat the family of diseases with which they are associated. This article is part of a Special Issue entitled: Recent advances in molecular engineering of antibody.
Copyright © 2014. Published by Elsevier B.V.

Entities:  

Keywords:  Amyloid; Antibody; Immunotherapy; Neurodegenerative disease; Protein-misfolding

Year:  2014        PMID: 25194824     DOI: 10.1016/j.bbapap.2014.08.016

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  29 in total

1.  Allosteric control of antibody-prion recognition through oxidation of a disulfide bond between the CH and CL chains.

Authors:  Jun Zhao; Ruth Nussinov; Buyong Ma
Journal:  Protein Eng Des Sel       Date:  2016-11-29       Impact factor: 1.650

2.  Mechanisms of recognition of amyloid-β (Aβ) monomer, oligomer, and fibril by homologous antibodies.

Authors:  Jun Zhao; Ruth Nussinov; Buyong Ma
Journal:  J Biol Chem       Date:  2017-09-18       Impact factor: 5.157

3.  Repurposing Triphenylmethane Dyes to Bind to Trimers Derived from Aβ.

Authors:  Patrick J Salveson; Sepehr Haerianardakani; Alexander Thuy-Boun; Stan Yoo; Adam G Kreutzer; Borries Demeler; James S Nowick
Journal:  J Am Chem Soc       Date:  2018-09-06       Impact factor: 15.419

4.  Silk micrococoons for protein stabilisation and molecular encapsulation.

Authors:  Ulyana Shimanovich; Francesco S Ruggeri; Erwin De Genst; Jozef Adamcik; Teresa P Barros; David Porter; Thomas Müller; Raffaele Mezzenga; Christopher M Dobson; Fritz Vollrath; Chris Holland; Tuomas P J Knowles
Journal:  Nat Commun       Date:  2017-07-19       Impact factor: 14.919

Review 5.  Conformational selection in amyloid-based immunotherapy: Survey of crystal structures of antibody-amyloid complexes.

Authors:  Buyong Ma; Jun Zhao; Ruth Nussinov
Journal:  Biochim Biophys Acta       Date:  2016-06-03

Review 6.  Transthyretin familial amyloid polyneuropathy: an update.

Authors:  Violaine Plante-Bordeneuve
Journal:  J Neurol       Date:  2017-12-16       Impact factor: 4.849

7.  "Trim"ming PolyQ proteins with engineered PML.

Authors:  Neha Dhar; Ammar Arsiwala; Shruthi Murali; Ravi S Kane
Journal:  Biotechnol Bioeng       Date:  2019-11-28       Impact factor: 4.530

8.  Latent analysis of unmodified biomolecules and their complexes in solution with attomole detection sensitivity.

Authors:  Emma V Yates; Thomas Müller; Luke Rajah; Erwin J De Genst; Paolo Arosio; Sara Linse; Michele Vendruscolo; Christopher M Dobson; Tuomas P J Knowles
Journal:  Nat Chem       Date:  2015-09-14       Impact factor: 24.427

9.  Visualizing and trapping transient oligomers in amyloid assembly pathways.

Authors:  Emma E Cawood; Theodoros K Karamanos; Andrew J Wilson; Sheena E Radford
Journal:  Biophys Chem       Date:  2020-11-10       Impact factor: 2.352

10.  Pre-amyloid oligomers of the proteotoxic RepA-WH1 prionoid assemble at the bacterial nucleoid.

Authors:  María Moreno-Del Álamo; Susana Moreno-Díaz de la Espina; M Elena Fernández-Tresguerres; Rafael Giraldo
Journal:  Sci Rep       Date:  2015-10-01       Impact factor: 4.379

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