Literature DB >> 7764903

Mutations and off-pathway aggregation of proteins.

R Wetzel1.   

Abstract

The off-pathway aggregation of proteins is a ubiquitous, yet poorly understood, phenomenon. In vitro, aggregation places limits on both protein stability and refolding yields. In vivo, it is responsible for inclusion-body formation in the bacterial production of proteins, as well as amyloid disease and related phenomena in animals. An important common feature of these processes is their sensitivity to point mutations, a feature that offers important clues for understanding controversial aspects of off-pathway aggregation such as its molecular specificity and the nature of the aggregating species. Results of a number of studies illustrate that the sensitivity of aggregation can derive from the ability of a mutation to either (1) facilitate the accumulation of a non-native state that is prone to aggregation, or (2) increase the intrinsic tendency of such a state to aggregate.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7764903     DOI: 10.1016/0167-7799(94)90082-5

Source DB:  PubMed          Journal:  Trends Biotechnol        ISSN: 0167-7799            Impact factor:   19.536


  66 in total

1.  Physicochemical consequences of amino acid variations that contribute to fibril formation by immunoglobulin light chains.

Authors:  R Raffen; L J Dieckman; M Szpunar; C Wunschl; P R Pokkuluri; P Dave; P Wilkins Stevens; X Cai; M Schiffer; F J Stevens
Journal:  Protein Sci       Date:  1999-03       Impact factor: 6.725

2.  Comparative Fourier transform infrared spectroscopy study of cold-, pressure-, and heat-induced unfolding and aggregation of myoglobin.

Authors:  Filip Meersman; László Smeller; Karel Heremans
Journal:  Biophys J       Date:  2002-05       Impact factor: 4.033

3.  Solvent-amino acid interaction energies in three-dimensional-lattice Monte Carlo simulations of a model 27-mer protein: Folding thermodynamics and kinetics.

Authors:  Kai Leonhard; John M Prausnitz; Clayton J Radke
Journal:  Protein Sci       Date:  2004-02       Impact factor: 6.725

4.  Thermal denaturation of Bungarus fasciatus acetylcholinesterase: Is aggregation a driving force in protein unfolding?

Authors:  I Shin; E Wachtel; E Roth; C Bon; I Silman; L Weiner
Journal:  Protein Sci       Date:  2002-08       Impact factor: 6.725

5.  Short amino acid stretches can mediate amyloid formation in globular proteins: the Src homology 3 (SH3) case.

Authors:  Salvador Ventura; Jesús Zurdo; Saravanakumar Narayanan; Matilde Parreño; Ramón Mangues; Bernd Reif; Fabrizio Chiti; Elisa Giannoni; Christopher M Dobson; Francesc X Aviles; Luis Serrano
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-03       Impact factor: 11.205

6.  Phase diagrams describing fibrillization by polyalanine peptides.

Authors:  Hung D Nguyen; Carol K Hall
Journal:  Biophys J       Date:  2004-10-01       Impact factor: 4.033

Review 7.  Physical chemistry of polyglutamine: intriguing tales of a monotonous sequence.

Authors:  Ronald Wetzel
Journal:  J Mol Biol       Date:  2012-01-27       Impact factor: 5.469

8.  Mutations can cause light chains to be too stable or too unstable to form amyloid fibrils.

Authors:  Marta Marin-Argany; Jofre Güell-Bosch; Luis M Blancas-Mejía; Sandra Villegas; Marina Ramirez-Alvarado
Journal:  Protein Sci       Date:  2015-09-07       Impact factor: 6.725

9.  Coarse-grained strategy for modeling protein stability in concentrated solutions. II: phase behavior.

Authors:  Vincent K Shen; Jason K Cheung; Jeffrey R Errington; Thomas M Truskett
Journal:  Biophys J       Date:  2005-12-30       Impact factor: 4.033

10.  Folding and aggregation of TEM beta-lactamase: analogies with the formation of inclusion bodies in Escherichia coli.

Authors:  G Georgiou; P Valax; M Ostermeier; P M Horowitz
Journal:  Protein Sci       Date:  1994-11       Impact factor: 6.725

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.