Expression and Purification of Recombinant Skd3 (Human ClpB) Protein and Tobacco Etch Virus (TEV) Protease from Escherichia coli

被引:8
|
作者
Cupo, Ryan [1 ,2 ]
Shorter, James [1 ,2 ]
机构
[1] Univ Penn, Dept Biochem & Biophys, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Pharmacol Grad Grp, Perelman Sch Med, Philadelphia, PA 19104 USA
来源
BIO-PROTOCOL | 2020年 / 10卷 / 23期
关键词
Skd3; CLPB; Protein disaggregase; Chaperone; TEV; Protein aggregation; 3-METHYLGLUTACONIC ACIDURIA; NEUTROPENIA; CATARACT; DISORDER;
D O I
10.21769/BioProtoc.3858
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Skd3 (encoded by human CLPB) is a mitochondrial AAA(+) protein comprised of an N-terminal ankyrin-repeat domain and a C-terminal HCLR-clade nucleotide-binding domain. The function of Skd3 has long remained unknown due to challenges in purifying the protein to high quality and near homogeneity. Recently we described Skd3 as a human mitochondrial protein disaggregase that solubilizes proteins in the mitochondrial intermembrane space. This protocol overcomes the challenges associated with purifying Skd3 and allows for in depth in vitro study of Skd3 activity. Tobacco etch virus (TEV) protease is required in the purification of Skd3. Thus, we also describe how to purify high quality TEV protease for use in the purification of Skd3, other purification protocols, and in vitro assays requiring TEV protease.
引用
收藏
页数:15
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