An Endoplasmic Reticulum Cyclophilin Cpr5p Rescues Z-type α1-Antitrypsin from Retarded Folding

Bulletin of the Korean chemical society

Kyunghee Lee¹  Chan-Hun Jung¹  Hana Im¹  Jeong Hun Lim¹ 

关键词: 1-Antitrypsin;    Cpr5p;    Peptidyl-prolyl isomerase;    Protein folding;   

DOI  :  

学科分类：化学（综合）

来源: Korean Chemical Society

【 摘 要 】

Human α1-antitrypsin (α1-AT) is a natural inhibitor of neutrophil elastases and has several dozens of genetic variants. Most of the deficient genetic variants of human α1-AT are unstable and cause pulmonary emphysema. However, the most clinically significant variant, Z-type α1-AT, exhibits retarded protein folding that leads to accumulation of folding intermediates. These aggregate within the endoplasmic reticulum (ER) of hepatocytes, subsequently causing liver cirrhosis as well as emphysema. Here, we studied the role of an ER folding assistant protein Cpr5p on Z-type α1-AT folding. Cpr5p was induced > 2-fold in Z-type α1-AT-expressing yeast cells compared with the wild type. Knockout of CPR5 exacerbated cytotoxicity of Z-type α1-AT, and re-introduction of CPR5 rescued the knockout cells from aggravated cytotoxicity caused by the α1-AT variant. Furthermore, Cpr5p co-immunoprecipitated with Z-type α1-AT and facilitated its protein folding. Our results suggest that protein-folding diseases may be suppressed by folding assistant proteins at the site of causal protein biosynthesis.

【 授权许可】

Unknown