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Syntheses of RNAs with up to 100 nucleotides containing site-specific 2'-methylseleno labels for use in X-ray crystallography

机译:用于X射线晶体学的具有100个核苷酸的RNA的合成,该RNA包含位点特异性2'-甲基硒代标记

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The derivatization of nucleic acids with selenium is a new and highly promising approach to facilitate their three-dimensional structure determination by X-ray crystallography. Here, we report a comprehensive study on the chemical and enzymatic syntheses of RNAs containing 2'-methylseleno (2'-Se-methyl) nucleoside labels. Our approach includes the first synthesis of an appropriate purine nucleoside phosphoramidite building block. Most importantly, a substantially changed RNA solid-phase synthesis cycle, comprising treatment with threo-1,4-dimercapto-2,3-butanediol (DTT) after the oxidation step, is required for a reliable strand elongation. This novel operation allows for the chemical syntheses of multiple Se-labeled RNAs in sizes that can typically be achieved only for nonmodified RNAs. In combination with enzymatic ligation, biologically important RNA targets become accessible for crystallography. Exemplarily, this has been demonstrated for the Diels-Alder ribozyme and the add adenine riboswitch sequences. We point out that the approach documented here has been the chemical basis for the very recent structure determination of the Diels-Alder ribozyme which represents the first novel RNA fold that has been solved via its Se-derivatives.
机译:用硒对核酸进行衍生化是一种新的且很有前途的方法,可促进通过X射线晶体学确定其三维结构。在这里,我们报告对包含2'-甲基硒(2'-Se-甲基)核苷标记的RNA的化学和酶促合成的综合研究。我们的方法包括首先合成适当的嘌呤核苷亚磷酰胺结构单元。最重要的是,为了可靠地延长链,需要实质上改变的RNA固相合成循环,包括在氧化步骤后用苏式1,4-二巯基-2,3-丁二醇(DTT)处理。这种新颖的操作可以化学合成多个Se-标记的RNA,大小通常只能通过未修饰的RNA来实现。结合酶促连接,生物学上重要的RNA靶标可用于晶体学。示例性地,对于Diels-Alder核酶和添加的腺嘌呤核糖开关序列已经证明了这一点。我们指出,此处记录的方法是Diels-Alder核酶最新结构测定的化学基础,该结构代表了首个通过其Se衍生物解决的新颖RNA折叠。

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