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用于获取“难以接近”肽段的拟脯氨酸(psi Pro)

Pseudo-prolines (psi Pro) for accessing "inaccessible" peptides.

作者信息

Mutter M, Nefzi A, Sato T, Sun X, Wahl F, Wöhr T

机构信息

Institute of Organic Chemistry, University of Lausanne, Switzerland.

出版信息

Pept Res. 1995 May-Jun;8(3):145-53.

PMID:7670229
Abstract

Pseudo-prolines (psi Pro) are introduced as a temporary protection technique for serine, threonine and cysteine side chains in standard Fmoc/tBu solid-phase peptide synthesis (SPPS). The incorporation of these novel building blocks into a growing peptide chain proceeds by means of the coupling of preformed, suitably protected psi Pro dipeptides. For the example of representative model peptides used in protein de novo design, the potential of psi Pro to solubilize otherwise sparingly or completely insoluble peptides is demonstrated. Because of their intrinsic propensity for preventing peptide aggregation and beta-sheet formation, pseudo-prolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques.

摘要

伪脯氨酸(psi Pro)作为一种临时保护技术被引入,用于标准的Fmoc/tBu固相肽合成(SPPS)中丝氨酸、苏氨酸和半胱氨酸侧链的保护。将这些新型结构单元掺入不断增长的肽链是通过预先形成的、适当保护的psi Pro二肽的偶联来实现的。对于蛋白质从头设计中使用的代表性模型肽的例子,展示了psi Pro使原本微溶或完全不溶的肽溶解的潜力。由于其内在的防止肽聚集和β-折叠形成的倾向,伪脯氨酸为通过汇聚策略和化学选择性连接技术获得大肽提供了新的可能性。

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