Literature DB >> 16520957

Micro-heterogeneity and aggregation in beta2-microglobulin solutions: effects of temperature, pH, and conformational variant addition.

Roberto Piazza1, Matteo Pierno, Sara Iacopini, Palma Mangione, Gennaro Esposito, Vittorio Bellotti.   

Abstract

We show that beta(2)-microglobulin solutions in physiological conditions contain a tiny fraction of aggregates, which can hardly be filtered out and tend to re-form spontaneously. At physiological pH the fractional amount and size distribution of the latter aggregates do not depend on temperature. Conversely, in the pH range typical of the peri-articular tissue acidosis that often occurs in hemodialysis, temperature increase leads to fast and irreversible growth of the aggregates. Quite similar, but strongly enhanced aggregation effects can be induced even in physiological conditions by adding a very small amount of DeltaN6, a naturally occurring truncated isoform of beta(2)-m known to promote fibrillogenesis.

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Year:  2006        PMID: 16520957     DOI: 10.1007/s00249-006-0051-0

Source DB:  PubMed          Journal:  Eur Biophys J        ISSN: 0175-7571            Impact factor:   1.733


  22 in total

1.  The solution structure of human beta2-microglobulin reveals the prodromes of its amyloid transition.

Authors:  Giuliana Verdone; Alessandra Corazza; Paolo Viglino; Fabio Pettirossi; Sofia Giorgetti; Palma Mangione; Alessia Andreola; Monica Stoppini; Vittorio Bellotti; Gennaro Esposito
Journal:  Protein Sci       Date:  2002-03       Impact factor: 6.725

Review 2.  Clinical relevance of cytokine production in hemodialysis.

Authors:  G Pertosa; G Grandaliano; L Gesualdo; F P Schena
Journal:  Kidney Int Suppl       Date:  2000-08       Impact factor: 10.545

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4.  Beta 2-microglobulin associated amyloidosis: a vanishing complication of long-term hemodialysis?

Authors:  S Schwalbe; M Holzhauer; J Schaeffer; M Galanski; K M Koch; J Floege
Journal:  Kidney Int       Date:  1997-10       Impact factor: 10.612

5.  Beta2-microglobulin induces caspase-dependent apoptosis in the CCRF-HSB-2 human leukemia cell line independently of the caspase-3, -8 and -9 pathways but through increased reactive oxygen species.

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Journal:  Proc Natl Acad Sci U S A       Date:  1998-05-26       Impact factor: 11.205

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Authors:  T T Ward; R T Steigbigel
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Authors:  T B Drüeke
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Journal:  J Biol Chem       Date:  1994-11-18       Impact factor: 5.157

10.  Different amyloidogenic peptides share a similar mechanism of neurotoxicity involving reactive oxygen species and calcium.

Authors:  M P Mattson; Y Goodman
Journal:  Brain Res       Date:  1995-04-03       Impact factor: 3.252

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  11 in total

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3.  Atomic structure of a nanobody-trapped domain-swapped dimer of an amyloidogenic beta2-microglobulin variant.

Authors:  Katarzyna Domanska; Saskia Vanderhaegen; Vasundara Srinivasan; Els Pardon; Florine Dupeux; Jose A Marquez; Sofia Giorgetti; Monica Stoppini; Lode Wyns; Vittorio Bellotti; Jan Steyaert
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-10       Impact factor: 11.205

4.  Monitoring the interaction between β2-microglobulin and the molecular chaperone αB-crystallin by NMR and mass spectrometry: αB-crystallin dissociates β2-microglobulin oligomers.

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Journal:  J Biol Chem       Date:  2013-05-03       Impact factor: 5.157

Review 5.  Understanding the complex mechanisms of β2-microglobulin amyloid assembly.

Authors:  Timo Eichner; Sheena E Radford
Journal:  FEBS J       Date:  2011-06-13       Impact factor: 5.542

Review 6.  Systemic amyloidosis: lessons from β2-microglobulin.

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Journal:  J Biol Chem       Date:  2015-03-06       Impact factor: 5.157

7.  Co-fibrillogenesis of Wild-type and D76N β2-Microglobulin: THE CRUCIAL ROLE OF FIBRILLAR SEEDS.

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Journal:  J Biol Chem       Date:  2016-02-26       Impact factor: 5.157

8.  C. elegans expressing human β2-microglobulin: a novel model for studying the relationship between the molecular assembly and the toxic phenotype.

Authors:  Luisa Diomede; Cristina Soria; Margherita Romeo; Sofia Giorgetti; Loredana Marchese; Patrizia Palma Mangione; Riccardo Porcari; Irene Zorzoli; Mario Salmona; Vittorio Bellotti; Monica Stoppini
Journal:  PLoS One       Date:  2012-12-21       Impact factor: 3.240

9.  Structure, folding dynamics, and amyloidogenesis of D76N β2-microglobulin: roles of shear flow, hydrophobic surfaces, and α-crystallin.

Authors:  P Patrizia Mangione; Gennaro Esposito; Annalisa Relini; Sara Raimondi; Riccardo Porcari; Sofia Giorgetti; Alessandra Corazza; Federico Fogolari; Amanda Penco; Yuji Goto; Young-Ho Lee; Hisashi Yagi; Ciro Cecconi; Mohsin M Naqvi; Julian D Gillmore; Philip N Hawkins; Fabrizio Chiti; Ranieri Rolandi; Graham W Taylor; Mark B Pepys; Monica Stoppini; Vittorio Bellotti
Journal:  J Biol Chem       Date:  2013-09-06       Impact factor: 5.157

Review 10.  Misfolding of amyloidogenic proteins and their interactions with membranes.

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Journal:  Biomolecules       Date:  2013-12-27
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