誤った折りたたみタンパク質が認知症に関与か(How misfolded proteins may contribute to Alzheimer’s, dementia)

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2025-07-11 ジョンズ・ホプキンス大学

ジョンズ・ホプキンス大学の研究で、アルツハイマー病や認知機能低下に関与する誤った折りたたみタンパク質が200種以上存在する可能性が判明。LiP‑MS技術を用いてラットの海馬を解析した結果、認知障害群に特有の構造異常タンパク質が多数見つかり、従来のアミロイドβやタウ以外の要因が浮上。これらは細胞の品質管理をすり抜けて蓄積し、病態に影響を与えるとされ、新たな診断・治療ターゲットとして期待される。

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ラットの老化モデルにおいて、認知に関連する構造変化を示すタンパク質は、再折り畳み能力が低下する Proteins with cognition-associated structural changes in a rat model of aging exhibit reduced refolding capacity

Haley E. Tarbox, Audrey Branch, and Stephen D. Fried
Science Advanses  Published:11 Jul 2025
DOI:https://doi.org/10.1126/sciadv.adt3778

誤った折りたたみタンパク質が認知症に関与か(How misfolded proteins may contribute to Alzheimer’s, dementia)

Abstract

Cognitive decline during aging represents a major societal burden, causing both personal and economic hardship in an increasingly aging population. Many studies have found that the proteostasis network, which functions to keep proteins properly folded, is impaired with age, suggesting that there may be many proteins that incur structural alterations with age. Here, we used limited proteolysis mass spectrometry, a structural proteomic method, to globally interrogate protein conformational changes in a rat model of cognitive aging. Specifically, we compared soluble hippocampal proteins from aged rats with preserved cognition to those from aged rats with impaired cognition. We identified a couple hundred proteins as having undergone cognition-associated structural changes (CASCs). We report that CASC proteins are substantially more likely to be nonrefoldable than non-CASC proteins, meaning that they typically cannot spontaneously refold to their native conformations after being chemically denatured. These findings suggest that noncovalent, conformational alterations may be general features in cognitive decline.

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