Spin Labeling and Characterization of Tau Fibrils Using Electron Paramagnetic Resonance (EPR)

• Published in: Methods in molecular biology (Clifton, N.J.) Vol. 1345; p. 185
• Main Authors: Meyer, Virginia, Margittai, Martin
• Format: Journal Article
• Language: English
• Published: United States 2016
• Subjects: Alzheimer Disease - genetics; Electron Spin Resonance Spectroscopy - methods; Humans; Spin Labels; tau Proteins - chemistry; tau Proteins - ultrastructure; DEER; Tau fibril; Alzheimer’s disease; Spin labeling; Amyloid; Protein structure; EPR spectroscopy
• ISSN: 1940-6029
• DOI: 10.1007/978-1-4939-2978-8_12

Template-assisted propagation of Tau fibrils is essential for the spreading of Tau pathology in Alzheimer's disease. In this process, small seeds of fibrils recruit Tau monomers onto their ends. The physical properties of the fibrils play an important role in their propagation. Here, we describe two different electron paramagnetic resonance (EPR) techniques that have provided crucial insights into the structure of Tau fibrils. Both techniques rely on the site-directed introduction of one or two spin labels into the protein monomer. Continuous-wave (CW) EPR provides information on which amino acid residues are contained in the fibril core and how they are stacked along the long fibril axis. Double electron-electron resonance (DEER) determines distances between two spin labels within a single protein and hence provides insights into their spatial arrangement in the fibril cross section. Because of the long distance range accessible to DEER (~2-5 nm) populations of distinct fibril conformers can be differentiated.