Journal Article

Redox-mediated regulation of an evolutionarily conserved cross-β structure formed by the TDP43 low complexity domain

Kato, Masato, Ghaemmaghami, Sina, Liu, Daifei, Zhou, Xiaoming, McKnight, Steven L., Tu, Benjamin P., Lin, Yi

2020

Overview

A methionine-rich low complexity (LC) domain is found within a C-terminal region of the TDP43 RNA-binding protein. Self-association of this domain leads to the formation of labile cross-β polymers and liquid-like droplets. Treatment with H₂O₂ caused phenomena of methionine oxidation and dropletmelting that were reversed upon exposure of the oxidized protein to methionine sulfoxide reductase enzymes. Morphological features of the cross-β polymers were revealed by H₂O₂-mediated footprinting. Equivalent TDP43 LC domain footprints were observed in polymerized hydrogels, liquid-like droplets, and living cells. The ability of H₂O₂ to impede cross-β polymerization was abrogated by the prominent M337V amyotrophic lateral sclerosis-causing mutation. These observations may offer insight into the biological role of TDP43 in facilitating synapse-localized translation as well as aberrant aggregation of the protein in neurodegenerative diseases.

• Publisher: National Academy of Sciences
• Subject: Amino Acid Sequence / Amyotrophic lateral sclerosis / Ataxin-2 - metabolism / Biochemistry / Biological Sciences / Complexity / Conserved Sequence / DNA-Binding Proteins - metabolism / Droplets / Footprinting / HEK293 Cells / Humans / Hydrogels / Hydrogen peroxide / Methionine / Mutation / Neurodegenerative diseases / Oxidation / Polymerization / Polymers / Protein Domains / Proteins / Reactive Oxygen Species - metabolism / Reductases / Ribonucleic acid / RNA / RNA-binding protein / Self-association