Hats off to 20S proteasome substrate discovery

被引：0

作者：

Church, Taylor R. ^{[1
]}

Brennan, Anna ^{[1
]}

Margolis, Seth S. ^{[1
,2
]}

机构：

[1] Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA

[2] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA

来源：

MOLECULAR SYSTEMS BIOLOGY | 2024年 / 20卷 / 04期

关键词：

PROTEIN; PATHWAY;

D O I：

10.1038/s44320-024-00028-7

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

Uncapped free 20S proteasomes are abundant and active in cells, and yet their degraded intracellular protein substrates have remained underexplored. In their recent study, Sharon and colleagues (Pepelnjak et al, 2024) developed an advanced proteomics method (PiP-MS) to comprehensively explore 20S proteasome substrates in the human proteome. The substrates of uncapped free 20S proteasomes have remained underexplored. In their recent study, Sharon, Picotti and colleagues (Pepelnjak et al, 2024) develop a proteomics-based method (PiP-MS) and comprehensively explore 20S proteasome substrates in the human proteome.

引用

页码：293 / 295

页数：3

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