Literature DB >> 30341605

High-Throughput Microplate-Based Fluorescence Assays for Studying Stochastic Aggregation of Superoxide Dismutase-1.

Alireza Abdolvahabi1, Sanaz Rasouli2,3, Corbin M Croom2, Devon L Plewman2.   

Abstract

Investigating in vitro kinetics of superoxide dismutase-1 (SOD1) aggregation with high-throughput microplate-based assays provides valuable information regarding SOD1 pathogenesis in amyotrophic lateral sclerosis (ALS) and opens venues for the development of effective therapies. In this chapter, we first explain the step-by-step purification and demetallation of wild-type (WT) and ALS-variant SOD1 proteins from Saccharomyces cerevisiae (baker's yeast). We then describe the methodology for a microplate-based fluorescence assay that is used to study real-time kinetics of metal-free (apo)-SOD1 aggregation. This technique is highly sensitive, semiautomated, requires minimum modifications to protein, and produces a plethora of data in a short period of time. We also describe a new approach for extracting clinically relevant information from SOD1 aggregation data using Kaplan-Meier estimators.

Entities:  

Keywords:  Amyloid; Amyotrophic lateral sclerosis; Cu, Zn superoxide dismutase; Demetallation; Fibrillization; Fluorescence spectroscopy; Protein purification; Thioflavin-T

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Year:  2019        PMID: 30341605     DOI: 10.1007/978-1-4939-8820-4_6

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  FAIM Opposes Aggregation of Mutant SOD1 That Typifies Some Forms of Familial Amyotrophic Lateral Sclerosis.

Authors:  Hiroaki Kaku; Alexander V Ludlow; Michael F Gutknecht; Thomas L Rothstein
Journal:  Front Neurosci       Date:  2020-02-21       Impact factor: 4.677

  1 in total

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