Aarhus University Seal / Aarhus Universitets segl

Oligomer diversity during the aggregation of the repeat-region of tau

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

Dokumenter

DOI

  • Magnus Kjaergaard
  • Alexander J. Dear, Cambridge University, Storbritannien
  • Franziska Kundel, Cambridge University, Storbritannien
  • Seema Qamar, University of Cambridge, Storbritannien
  • Georg Meisl, Cambridge University, Storbritannien
  • Tuomas P.J. Knowles, Cambridge University, Storbritannien
  • David Klenerman, Cambridge University, Storbritannien

The molecular mechanism of protein aggregation is of both fundamental and clinical importance as amyloid aggregates are linked to a number of neurodegenerative disorders. Such protein aggregates include macroscopic insoluble fibrils as well as small soluble oligomeric species. Time-dependent resolution of these species is prerequisite for a detailed quantitative understanding of protein aggregation; this remains challenging due to the lack of methods for detecting and characterizing transient and heterogeneous protein oligomers. Here we have used single molecule fluorescence techniques combined with mechanistic modelling to study the heparin-induced aggregation of the repeat region of tau, which forms the core region of neurofibrillary tangles found in Alzheimer's disease. We distinguish several sub-populations of oligomers with different stability and follow their evolution during aggregation reactions as a function of temperature and concentration. Employment of techniques from chemical kinetics reveals that the two largest populations structurally distinct from fibrils; and are both kinetically and thermodynamically unstable. The first population is in rapid exchange with monomers and held together by electrostatic interactions; the second is kinetically more stable, dominates at later times and is probably off-pathway to fibril formation. These more stable oligomers may contribute to other oligomer induced effects in the cellular environment, for example by overloading protein quality control systems. We also show that the shortest growing filaments remain suspended in aqueous buffer and thus comprise a third, smaller population of transient oligomers with cross-i¢ structure. Overall our data show that a diverse population of oligomers of different structures and half-lives are formed during the aggregation reaction with the great majority of oligomers formed not going on to form fibrils.

OriginalsprogEngelsk
TidsskriftACS Chemical Neuroscience
Vol/bind9
Nummer12
Sider (fra-til)3060-3071
Antal sider12
ISSN1948-7193
DOI
StatusUdgivet - 2018

Se relationer på Aarhus Universitet Citationsformater

Download-statistik

Ingen data tilgængelig

ID: 137075746