Key Laboratory of Plant Protection Resources and Pest Management of Ministry of Education, Northwest A&F University, Yangling 712100, China.
Int J Mol Sci. 2013 Dec 16;14(12):24501-13. doi: 10.3390/ijms141224501.
Protein phosphatase 5 (PP5) is a unique member of serine/threonine phosphatases which has been recognized in regulation of diverse cellular processes. A cDNA fragment encoding PP5 (EcPP5) was cloned and characterized from the cantharidin-producing blister beetle, E. chinensis. EcPP5 contains an open reading frame of 1500 bp that encodes a protein of 56.89 kDa. The deduced amino acid sequence shares 88% and 68% identities to the PP5 of Tribolium castaneum and humans, respectively. Analysis of the primary sequence shows that EcPP5 has three TPR (tetratricopeptide repeat) motifs at its N-terminal region and contains a highly conserved C-terminal catalytic domain. RT-PCR reveals that EcPP5 is expressed in all developmental stages and in different tissues. The recombinant EcPP5 (rEcPP5) was produced in Escherichia coli and purified to homogeneity. The purified protein exhibited phosphatase activity towards pNPP (p-nitrophenyl phosphate) and phosphopeptides, and its activity can be enhanced by arachidonic acid. In vitro inhibition study revealed that protein phosphatase inhibitors, okadaic acid, cantharidin, norcantharidin and endothall, inhibited its activity. Further, protein phosphatase activity of total soluble protein extract from E. chinensis adults could be impeded by these inhibitors suggesting there might be some mechanism to protect this beetle from being damaged by its self-produced cantharidin.
蛋白磷酸酶 5(PP5)是丝氨酸/苏氨酸磷酸酶家族中的一个独特成员,其在调节多种细胞过程中发挥作用。本研究从芫菁科(Meloidae)的斑芫菁(Eupomphalia chinensis)中克隆并鉴定了编码 PP5(EcPP5)的 cDNA 片段。EcPP5 含有一个 1500bp 的开放阅读框,编码一个 56.89kDa 的蛋白质。推导的氨基酸序列与赤拟谷盗(Tribolium castaneum)和人类的 PP5 分别具有 88%和 68%的同源性。序列分析表明,EcPP5 在其 N 端区域含有三个 TPR(四肽重复)基序,并含有高度保守的 C 端催化结构域。RT-PCR 结果显示 EcPP5 在各个发育阶段和不同组织中均有表达。重组 EcPP5(rEcPP5)在大肠杆菌中表达并纯化至均一性。该纯化蛋白对 pNPP(对硝基苯磷酸)和磷酸肽表现出磷酸酶活性,且其活性可被花生四烯酸增强。体外抑制研究表明,蛋白磷酸酶抑制剂(冈田酸、斑蝥素、去斑蝥素和涕灭威)抑制了其活性。此外,斑蝥素自毒作用可能通过抑制蛋白磷酸酶活性来保护斑芫菁免受其自身产生的斑蝥素的损害。