自噬
泛素
果蝇属(亚属)
细胞生物学
焊剂(冶金)
蛋白酶体
支架蛋白
化学
蛋白质降解
生物
生物化学
基因
信号转导
有机化学
细胞凋亡
作者
Lindsay DeVorkin,Sharon M. Gorski
出处
期刊:CSH Protocols
[Cold Spring Harbor Laboratory Press]
日期:2014-09-01
卷期号:2014 (9): pdb.prot080333-pdb.prot080333
被引量:28
标识
DOI:10.1101/pdb.prot080333
摘要
Human p62, also known as Sequestome-1 (SQSTM1), is a multifunctional scaffold protein that contains many domains, including a Phox/Bem1P (PB1) multimerization domain, an ubiquitin-associated (UBA) domain, and a light chain 3 (LC3) recognition sequence. p62 binds ubiquitinated proteins and targets them for degradation by the proteasome. In addition, p62 directly binds LC3; this may serve as a mechanism to deliver ubiquitinated proteins for degradation by autophagy. During this process, p62 itself is degraded. The inhibition of autophagy leads to the accumulation of p62, indicating that it can be used as a marker of autophagic flux. Ref(2)P (refractory to sigma P), the Drosophila ortholog of p62, is also required for the formation of ubiquitinated protein aggregates. Ref(2)P contains a putative LC3-interacting region, and genetic inhibition of autophagy in Drosophila leads to the accumulation of Ref(2)P protein levels. Thus, like p62, Ref(2)P may serve as a marker of autophagic flux. Here we provide two procedures to examine Ref(2)P protein levels in Drosophila ovaries.
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