Literature DB >> 15283924

Techniques to study amyloid fibril formation in vitro.

Melanie R Nilsson1.   

Abstract

Amyloid fibrils are ordered aggregates of peptides or proteins that are fibrillar in structure and contribute to the complications of many diseases (e.g., type 2 diabetes mellitus, Alzheimer's disease, and primary systemic amyloidosis). These fibrils can also be prepared in vitro and there are three criteria that define a protein aggregate as an amyloid fibril: green birefringence upon staining with Congo Red, fibrillar morphology, and beta-sheet secondary structure. The purpose of this review is to describe the techniques used to study amyloid fibril formation in vitro, address common errors in the collection and interpretation of data, and open a discussion for a critical review of the criteria currently used to classify a protein aggregate as an amyloid fibril.

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Year:  2004        PMID: 15283924     DOI: 10.1016/j.ymeth.2004.03.012

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  190 in total

1.  Inhibitors of amyloid toxicity based on beta-sheet packing of Abeta40 and Abeta42.

Authors:  Takeshi Sato; Pascal Kienlen-Campard; Mahiuddin Ahmed; Wei Liu; Huilin Li; James I Elliott; Saburo Aimoto; Stefan N Constantinescu; Jean-Noel Octave; Steven O Smith
Journal:  Biochemistry       Date:  2006-05-02       Impact factor: 3.162

2.  Hydrogen exchange mass spectrometry as an analytical tool for the analysis of amyloid fibrillogenesis.

Authors:  Carsten Scavenius; Shirin Ghodke; Daniel E Otzen; Jan J Enghild
Journal:  Int J Mass Spectrom       Date:  2011-04-30       Impact factor: 1.986

3.  The impact of solubility and electrostatics on fibril formation by the H3 and H4 histones.

Authors:  Traci B Topping; Lisa M Gloss
Journal:  Protein Sci       Date:  2011-11-09       Impact factor: 6.725

4.  Response surface methodology for optimizing the bovine serum albumin fibrillation.

Authors:  Amir Arasteh; Mehran Habibi-Rezaei; Azadeh Ebrahim-Habibi; Ali Akbar Moosavi-Movahedi
Journal:  Protein J       Date:  2012-08       Impact factor: 2.371

5.  A generic crystallization-like model that describes the kinetics of amyloid fibril formation.

Authors:  Rosa Crespo; Fernando A Rocha; Ana M Damas; Pedro M Martins
Journal:  J Biol Chem       Date:  2012-07-05       Impact factor: 5.157

6.  Understanding amyloid aggregation by statistical analysis of atomic force microscopy images.

Authors:  Jozef Adamcik; Jin-Mi Jung; Jérôme Flakowski; Paolo De Los Rios; Giovanni Dietler; Raffaele Mezzenga
Journal:  Nat Nanotechnol       Date:  2010-04-11       Impact factor: 39.213

Review 7.  Fluorescence spectroscopy of protein oligomerization in membranes.

Authors:  Galyna P Gorbenko
Journal:  J Fluoresc       Date:  2010-04-06       Impact factor: 2.217

8.  Detection of populations of amyloid-like protofibrils with different physical properties.

Authors:  Annalisa Relini; Silvia Torrassa; Riccardo Ferrando; Ranieri Rolandi; Silvia Campioni; Fabrizio Chiti; Alessandra Gliozzi
Journal:  Biophys J       Date:  2010-04-07       Impact factor: 4.033

9.  Tracking the heterogeneous distribution of amyloid spherulites and their population balance with free fibrils.

Authors:  V Foderà; A M Donald
Journal:  Eur Phys J E Soft Matter       Date:  2010-11-04       Impact factor: 1.890

10.  Conformational transitions provoked by organic solvents in chicken egg ovalbumin: mimicking the local environment.

Authors:  Afshin Iram; Aabgeena Naeem
Journal:  Protein J       Date:  2013-01       Impact factor: 2.371

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