α-和β-含谷氨酸侧链寡聚谷氨酸定长微管蛋白合成多肽。

International Journal of Peptides Pub Date : 2010-01-01 Epub Date: 2010-12-15 DOI:10.1155/2010/189396
Werner Tegge, Carlos F S Bonafe, Aileen Teichmann, Christian Erck
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引用次数: 3

摘要

侧链寡聚谷氨酰化是微管蛋白生理学中一个重要的翻译后修饰。谷氨酸单位的特定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构建块的方法,用于Fmoc合成含有主链谷氨酸残基的肽,这些残基带有低聚谷氨酸的侧链分支。从哺乳动物α1-微管蛋白和β1-微管蛋白的c端分别组装了两个模型肽序列CYEEVGVDSVEGEG-E(E(x))- eegeey和CQDATADEQG-E(E(x))- feeeegedea,它们含有长度为1 ~ 5个氨基酸的低聚谷氨酸侧链分支。这些产物可能导致产生特异性抗体,这将是对多谷氨酰化过程进行更详细研究的重要工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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(E(x))-EEGEEY and CQDATADEQG-E(E(x))-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.

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