Recombinant expression, purification, and crystallization of the sterile α-motif/histidine-aspartate domain-containing protein from chicken

被引:0
|
作者
Li, Yanhong [1 ]
Peng, Xin [1 ]
Qin, Xiaohong [1 ]
机构
[1] Tianjin Univ, Sch Sci, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
dNTPase; Enzyme catalysis; Restriction factor; Innate immunity; AICARDI-GOUTIERES SYNDROME; RESTRICTION FACTOR SAMHD1; CD4(+) T-CELLS; HIV-1; RESTRICTION; TRIPHOSPHATE TRIPHOSPHOHYDROLASE; DGTP TRIPHOSPHOHYDROLASE; ENTEROCOCCUS-FAECALIS; ESCHERICHIA-COLI; DENDRITIC CELLS; BINDING-PROTEIN;
D O I
10.1016/j.pep.2016.04.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The sterile alpha-motif and HD domain containing protein 1 (SAMHD1) family is a newly identified protein family, involved in innate immunity restriction. This family possesses a broad-spectrum of antiviral activity. The SAMHD1 family in chicken has not been clearly documented. Here, we expressed chicken SAMHD1 (101-614) fused with a SUMO tag in an Escherichia coli (E. coli) system. For the first time, chicken SAMHD1 (101-614) was found to possess dNTPase cleavage activities in vitro. This suggests that chicken SAMHD1 may be a potential antiviral factor against avian viruses. Through a unique purification method, the purity of the protein as estimated by SDS-PAGE was >95% after a double Ni affinity chromatography and gel filtration purification. Using a sitting-drop vapor-diffusion method, protein crystals were obtained. This study provides some essential method and information for further structure and function determinations of chicken SAMHD1. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:96 / 101
页数:6
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