8A6I

Structure of the low complexity domain of TDP-43 (fragment 309-350) with methionine sulfoxide modifications

8A6I の概要

• エントリーDOI: 10.2210/pdb8a6i/pdb
• NMR情報: BMRB: 34737
• 分子名称: TAR DNA-binding protein 43 (1 entity in total)
• 機能のキーワード: tdp-43, low complexity domain, prion-like domain, methionine sulfoxide, llps, unknown function
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 4331.80

構造登録者

Carrasco, J.,Anton, R.,Pantoja-Uceda, D.,Laurents, D.V.,Oroz, J. (登録日: 2022-06-17, 公開日: 2023-02-08, 最終更新日: 2024-10-23)

主引用文献

Carrasco, J.,Anton, R.,Valbuena, A.,Pantoja-Uceda, D.,Mukhi, M.,Hervas, R.,Laurents, D.V.,Gasset, M.,Oroz, J.
Metamorphism in TDP-43 prion-like domain determines chaperone recognition.
Nat Commun, 14:466-466, 2023

PubMed Abstract: The RNA binding protein TDP-43 forms cytoplasmic inclusions via its C-terminal prion-like domain in several neurodegenerative diseases. Aberrant TDP-43 aggregation arises upon phase de-mixing and transitions from liquid to solid states, following still unknown structural conversions which are primed by oxidative stress and chaperone inhibition. Despite the well-established protective roles for molecular chaperones against protein aggregation pathologies, knowledge on the determinants of chaperone recognition in disease-related prions is scarce. Here we show that chaperones and co-chaperones primarily recognize the structured elements in TDP-43´s prion-like domain. Significantly, while HSP70 and HSP90 chaperones promote TDP-43 phase separation, co-chaperones from the three classes of the large human HSP40 family (namely DNAJA2, DNAJB1, DNAJB4 and DNAJC7) show strikingly different effects on TDP-43 de-mixing. Dismantling of the second helical element in TDP-43 prion-like domain by methionine sulfoxidation impacts phase separation and amyloid formation, abrogates chaperone recognition and alters phosphorylation by casein kinase-1δ. Our results show that metamorphism in the post-translationally modified TDP-43 prion-like domain encodes determinants that command mechanisms with major relevance in disease.

PubMed: 36709343
DOI: 10.1038/s41467-023-36023-z

実験手法

SOLUTION NMR