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NXO Building Blocks for Backbone Modification of Peptides and Preparation of Pseudopeptides

机译:用于肽的骨干修饰和伪肽制备的NXO构建基块

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The design and synthesis of novel building blocks for peptide modification, termed “NXO”, is reported. We describe the utility of these building blocks to prepare new pseudo- and oligopeptides and demonstrate the efficient assembly of modified tripeptides using both conventional liquid phase peptide synthesis and solid supported synthesis. Pertaining to the study of NXO in peptide mimicry, the structure of NXO-incorporating tripeptide β-strand mimics was investigated in the NLAlaO incorporating β-sheet model compound 13. Evidenced by spectroscopy and computation, 13 selectively adopts a β-structure in chloroform and characteristically samples the NXO-modified backbone site in the core β-sheet region.ROESY(HNMR)and molecular dynamics data suggest that when disrupting the cross-strand hydrogen-bonding pattern by switching the solvent from CDCl3 to d3-MeOH, the main conformation with peptide and NXO-peptide backbones similar to that in root mean square deviation of corresponding backbone atoms (rmsd) is preserved.
机译:报告了称为“ NXO”的新型肽修饰基团的设计和合成。我们描述了这些构件的实用程序,以制备新的假肽和寡肽,并证明了使用常规液相肽合成和固相支持合成的修饰三肽的有效组装。为了研究肽模拟中的NXO,在掺有β-折叠模型化合物13的NLAlaO中研究了掺入NXO的三肽β-链模拟物的结构。通过光谱和计算证明,13在氯仿中选择性地采用β结构, ROESY(HNMR)和分子动力学数据表明,当通过将溶剂从CDCl3切换为d3-MeOH来破坏跨链氢键模式时,主要构象为ROESY(HNMR)和分子动力学数据其肽和NXO肽主链与根的均方根(rmsd)的均方根相似。

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