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首页> 外文期刊>Journal of biological inorganic chemistry: JBIC: a publication of the Society of Biological Inorganic Chemistry >Incorporation of the red copper nitrosocyanin binding loop into blue copper azurin
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Incorporation of the red copper nitrosocyanin binding loop into blue copper azurin

机译:将红铜亚硝基花青素结合环结合到蓝铜天青素中

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Loop-directed mutagenesis was applied to the blue copper protein azurin to replace its copper binding loop with that from the red copper protein nitrosocyanin. A ten amino acid long loop that provides three of the four copper ligands from nitrosocyanin was incorporated into azurin to make a variant called NC-azurin. The chimeric protein displayed a red color, and UV-vis absorption and EPR spectra that closely resembled those of the loop parent, nitrosocyanin. We added the fourth ligand from nitrosocyanin into NC-azurin, a carboxylate-containing amino acid, but the proteins had altered stability and spectroscopic properties that did not resemble those of either parent copper protein. The loop alone, however, was enough to impart red copper site characteristics to the NC-azurin protein. Finally, the reduction potential of the variant was found to be between the reduction potentials of the parent proteins and about 50 mV below that of wildtype azurin.
机译:将环定向诱变应用于蓝色铜蛋白天青蛋白,以其铜结合环替换为红色铜蛋白亚硝基花青素。将提供亚硝基花青素的四个铜配体中的三个的十个氨基酸长的环并入天青素中,制成称为NC-天青素的变体。嵌合蛋白显示红色,紫外可见吸收和EPR光谱与环亲本亚硝基花青素非常相似。我们将亚硝基花青素中的第四个配体添加到了含羧酸盐的氨基酸NC-天青素中,但是这些蛋白质的稳定性和光谱特性发生了变化,与任何一种母体铜蛋白都不一样。然而,仅该环就足以将红铜位点特征赋予NC-天青蛋白。最后,发现该变体的还原电位在亲本蛋白的还原电位与野生型天青蛋白的还原电位之间约50mV。

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