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Synthesis of Peptides from α- and β-Tubulin Containing Glutamic Acid Side-Chain Linked Oligo-Glu with Defined Length

机译:由确定长度的含谷氨酸侧链连接的寡聚谷氨酸的α-和β-木瓜蛋白酶合成肽

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摘要

Side-chain oligo- and polyglutamylation represents an important posttranslational modification in tubulin physiology. The particular number of glutamate units is related to specific regulatory functions. In this work, we present a method for the synthesis of building blocks for the Fmoc synthesis of peptides containing main chain glutamic acid residues that carry side-chain branching with oligo-glutamic acid. The two model peptide sequences CYEEVGVDSVEGEG-E(Ex)-EEGEEY and CQDATADEQG-E(Ex)-FEEEEGEDEA from the C-termini of mammalian α1- and β1-tubulin, respectively, containing oligo-glutamic acid side-chain branching with lengths of 1 to 5 amino acids were assembled in good yield and purity. The products may lead to the generation of specific antibodies which should be important tools for a more detailed investigation of polyglutamylation processes.
机译:侧链寡和聚谷氨酰化代表微管蛋白生理学中重要的翻译后修饰。谷氨酸单位的具体数量与特定的调节功能有关。在这项工作中,我们提出了一种合成模块的合成方法,该模块用于Fmoc合成含有主链谷氨酸残基的肽,这些残基带有带有寡谷氨酸的侧链分支。来自哺乳动物α1-和β1-微管蛋白C末端的两个模型肽序列CYEEVGVDSVEGEG-E(Ex)-EEGEEY和CQDATADEQG-E(Ex)-FEEEEGEDEA,分别含有寡谷氨酸侧链支链,长度为1-5个氨基酸以高收率和纯度组装。该产品可能会导致产生特异性抗体,这应该是更详细研究聚谷氨酰化过程的重要工具。

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