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Determination of the DNA-binding kinetics of three related but heteroimmune bacteriophage repressors using EMSA and SPR analysis

机译:使用EMSA和SPR分析确定三种相关但异种免疫噬菌体阻遏物的DNA结合动力学

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摘要

Bacteriophages P2, P2 Hy dis and WΦ are very similar but heteroimmune Escherichia coli phages. The structural genes show over 96% identity, but the repressors show between 43 and 63% identities. Furthermore, the operators, which contain two directly repeated sequences, vary in sequence, length, location relative to the promoter and spacing between the direct repeats. We have compared the in vivo effects of the wild type and mutated operators on gene expression with the complexes formed between the repressors and their wild type or mutated operators using electrophoretic mobility shift assay (EMSA), and real-time kinetics of the protein–DNA interactions using surface plasmon resonance (SPR) analysis. Using EMSA, the repressors formed different protein–DNA complexes, and only WΦ was significantly affected by point mutations. However, SPR analysis showed a reduced association rate constant and an increased dissociation rate constant for P2 and WΦ operator mutants. The association rate constants of P2 Hy dis was too fast to be determined. The P2 Hy dis dissociation response curves were shown to be triphasic, while both P2 and WΦ C were biphasic. Thus, the kinetics of complex formation and the nature of the complexes formed differ extensively between these very closely related phages.
机译:噬菌体P2,P2 Hy dis和WΦ非常相似,但具有异免疫力的大肠杆菌噬菌体。结构基因显示超过96%的同一性,但阻遏物显示43%至63%的同一性。此外,包含两个直接重复序列的操纵子在序列,长度,相对于启动子的位置以及直接重复之间的间隔上有所不同。我们使用电泳迁移率变动分析(EMSA)和蛋白质-DNA的实时动力学,比较了野生型和突变的操纵基因对基因表达的体内作用与阻遏物与其野生型或突变的操纵基因之间形成的复合物。表面等离振子共振(SPR)分析的相互作用。使用EMSA,阻遏物形成了不同的蛋白质-DNA复合物,只有WΦ受点突变显着影响。但是,SPR分析显示P2和WΦ操纵子突变体的缔合速率常数降低,解离速率常数升高。 P2 Hy dis的缔合速率常数太快,无法确定。 P2 Hy解离反应曲线显示为三相,而P2和WΦC均为双相的。因此,在这些非常密切相关的噬菌体之间,复合物形成的动力学和形成的复合物的性质差异很大。

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