Sehrawat Seema, Srinivasan Narayanaswamy, Gopinathan Karumathil P
Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India.
Biochem J. 2002 Nov 15;368(Pt 1):159-69. doi: 10.1042/BJ20020456.
Late gene expression factor 4 (LEF4), a multifunctional protein encoded by the Bombyx mori nucleopolyhedrovirus has been bacterially expressed and characterized. Sequence analyses and three-dimensional modelling of B. mori LEF4 showed that the protein is related to mRNA-capping enzymes, which are organized as two modular domains. Most of the acidic side chains in LEF4 were solvent-exposed and spread all along the fold. A region dominated by negatively charged groups, which protrudes from the larger domain was ideally suited for interactions with proteins having positively charged patches at the surface. The purified LEF4 protein exhibited different enzyme activities associated with mRNA-capping enzymes, i.e. GTP-binding, RNA triphosphatase and guanylate transferase activities. In addition, LEF4 also showed NTP-hydrolysing activity. The kinetic analysis of ATP hydrolysis revealed a sigmoidal response with two deduced binding sites for ATP, whereas the guanylate transferase activity showed a typical hyperbolic response to varying concentrations of GTP with a Km of 330+/-20 microM. Analysis of the modelled three-dimensional structure of LEF4 suggested the presence of crucial residues in sequence motifs important for the integrity of the fold. Mutation of one such conserved and buried tyrosine residue to cysteine in the motif IIIa, located close to the interlobe region of the model, resulted in a 44% loss of guanylate transferase activity of LEF4 but had no effect on the ATPase activity.
家蚕核型多角体病毒编码的多功能蛋白晚期基因表达因子4(LEF4)已在细菌中表达并进行了特性鉴定。家蚕LEF4的序列分析和三维建模表明,该蛋白与mRNA加帽酶有关,mRNA加帽酶由两个模块化结构域组成。LEF4中的大多数酸性侧链都暴露于溶剂中,并沿折叠结构分布。从较大结构域突出的一个以带负电荷基团为主的区域非常适合与表面带有带正电荷斑块的蛋白质相互作用。纯化的LEF4蛋白表现出与mRNA加帽酶相关的不同酶活性,即GTP结合、RNA三磷酸酶和鸟苷酸转移酶活性。此外,LEF4还表现出NTP水解活性。ATP水解的动力学分析显示出具有两个推导的ATP结合位点的S形响应,而鸟苷酸转移酶活性对不同浓度的GTP表现出典型的双曲线响应,Km为330±20 microM。对LEF4的三维建模结构分析表明,在对折叠结构完整性很重要的序列基序中存在关键残基。在靠近模型叶间区域的基序IIIa中,将一个这样保守且埋藏的酪氨酸残基突变为半胱氨酸,导致LEF4的鸟苷酸转移酶活性丧失44%,但对ATP酶活性没有影响。