降级(电信)
控制(管理)
蛋白质质量
化学
质量(理念)
计算生物学
细胞生物学
生物化学
计算机科学
生物
人工智能
物理
电信
量子力学
作者
Leonie Müller,Thorsten Hoppe
标识
DOI:10.1016/j.tibs.2024.06.006
摘要
The degradation of damaged proteins is critical for tissue integrity and organismal health because damaged proteins have a high propensity to form aggregates. E3 ubiquitin ligases are key regulators of protein quality control (PQC) and mediate the selective degradation of damaged proteins, a process termed 'PQC degradation' (PQCD). The degradation signals (degrons) that trigger PQCD are based on hydrophobic sites that are normally buried within the native protein structure. However, an open question is how PQCD-specialized E3 ligases distinguish between transiently misfolded proteins, which can be efficiently refolded, and permanently damaged proteins, which must be degraded. While significant progress has been made in characterizing degradation determinants, understanding the key regulatory signals of cellular and organismal PQCD pathways remains a challenge.
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