Application and analysis of the GFPu family of ubiquitin-proteasome system reporters
被引:73
作者:
Bence, NF
论文数: 0引用数: 0
h-index: 0
机构:
Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USAStanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
Bence, NF
[1
]
Bennett, EJ
论文数: 0引用数: 0
h-index: 0
机构:
Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USAStanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
Bennett, EJ
[1
]
Kopito, RR
论文数: 0引用数: 0
h-index: 0
机构:
Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USAStanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
Kopito, RR
[1
]
机构:
[1] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
来源:
UBIQUITIN AND PROTEIN DEGRADATION, PT B
|
2005年
/
399卷
关键词:
D O I:
10.1016/S0076-6879(05)99033-2
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
The relevance of the ubiquitin proteasome system (UPS) to disease and fundamental cellular processes has generated a demand for methods to monitor the activity of this system in living cells and organisms. Here we describe the GFP(u) family of UPS reporters. These reporters are constitutively degraded, ubiquitin-dependent proteasome substrates that can be used to monitor UPS function in the living cell. The GFP(u) reporter family consists of three variants that can report on global, nuclear, and cytoplasmic UPS function. This article focuses on the properties and design of these reporters and highlights appropriate techniques and applications for their use.