Preparation of stable tau oligomers for cellular and biochemical studies

Thomas K. Karikari, David A. Nagel, Alastair Grainger, Charlotte Clarke-bland, Eric J. Hill, Kevin G. Moffat

Research output: Contribution to journalArticle

Abstract

Increasing evidence suggests that small oligomers are the principal neurotoxic species of tau in Alzheimer's disease and other tauopathies. However, mechanisms of tau oligomer-mediated neurodegeneration are poorly understood. The transience of oligomers due to aggregation can compromise the stability of oligomers prepared in vitro. Consequently, we sought to develop an efficient method which maintains the stability and globular conformation of preformed oligomers. This study demonstrates that labeling a single-cysteine form of the pro-aggregant tau four-repeat region (K18) with either Alexa Fluor 488-C5-maleimide or N-ethylmaleimide in reducing conditions stabilizes oligomers by impeding their further aggregation. Furthermore, the use of this approach to study the propagation of labeled extracellular tau K18 oligomers into human neuroblastoma cells and human stem cell-derived neurons is described. This method is potentially applicable for preparing stabilized oligomers of tau for diagnostic and biomarker tests, as well as for in vitro structure-activity relationship assays.
Original languageEnglish
Pages (from-to)67-74
Number of pages8
JournalAnalytical Biochemistry
Volume566
Early online date11 Oct 2018
DOIs
Publication statusPublished - 1 Feb 2019

Bibliographical note

© 2018 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http://creativecommons.org/licenses/BY/4.0/)

Funding: National Centre for the Replacement, Refinement and Reduction of Animals in Research (grant NC/C013101/1); Biotechnology and Biological Sciences Research Council grant number BB/J014532/1.

Keywords

  • Alzheimer's disease
  • iPSC-derived neurons
  • Maleimide
  • Oligomer
  • Tau
  • Tauopathies

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