Wheeler Brody, Jia Zongchao
Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Ont. K7L 3N6, Canada.
Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Ont. K7L 3N6, Canada.
Protein Expr Purif. 2015 Apr;108:13-17. doi: 10.1016/j.pep.2014.12.008. Epub 2014 Dec 22.
AarF domain containing kinase 3 (ADCK3) is a mitochondrial protein known to have a role in the electron transport chain. Despite being required for the biosynthesis of coenzyme Q10, a lipid-soluble electron transporter found to be essential for aerobic cellular respiration, the precise biological function of ADCK3 remains unknown. Patients with mutations in ADCK3 experience an onset of neurological disorders from childhood, including cerebellar ataxia and exercise intolerance. After extensive screening for soluble recombinant protein expression, an N-terminal fusion of maltose-binding protein was found to facilitate the overexpression of the human ADCK3 kinase domain in Escherichia coli as a soluble and biologically active entity. For the first time our work reveals Mg(2+)-dependent ATPase activity of ADCK3, providing strong support for the theoretical prediction of this protein being a functional atypical kinase.
含AarF结构域激酶3(ADCK3)是一种线粒体蛋白,已知其在电子传递链中发挥作用。尽管辅酶Q10的生物合成需要ADCK3,辅酶Q10是一种脂溶性电子转运体,对有氧细胞呼吸至关重要,但ADCK3的确切生物学功能仍不清楚。ADCK3发生突变的患者从儿童期就开始出现神经疾病,包括小脑共济失调和运动不耐受。在对可溶性重组蛋白表达进行广泛筛选后,发现麦芽糖结合蛋白的N端融合有助于人ADCK3激酶结构域在大肠杆菌中作为可溶性生物活性实体进行过表达。我们的工作首次揭示了ADCK3的Mg(2+)依赖性ATP酶活性,为该蛋白是一种功能性非典型激酶的理论预测提供了有力支持。