伪脯氨酸(psi Pro)用于获取“不可接近”的肽。

Peptide research Pub Date : 1995-05-01
M Mutter, A Nefzi, T Sato, X Sun, F Wahl, T Wöhr
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引用次数: 0

摘要

介绍了伪脯氨酸(psi Pro)作为标准Fmoc/tBu固相肽合成(SPPS)中丝氨酸、苏氨酸和半胱氨酸侧链的临时保护技术。将这些新的构建块结合到不断增长的肽链中,通过预先形成的、适当保护的psi Pro二肽的偶联进行。对于在蛋白质从头设计中使用的代表性模型肽的例子,psi Pro的潜力可以溶解少量或完全不溶的肽。由于其内在倾向于阻止肽聚集和β -片的形成,伪脯氨酸为通过聚合策略和化学选择性连接技术获得大肽提供了新的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pseudo-prolines (psi Pro) for accessing "inaccessible" peptides.

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.

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