化学
肽
丝氨酸
半胱氨酸
苏氨酸
组合化学
固相合成
肽合成
化学结扎
侧链
氨基酸
立体化学
生物化学
有机化学
磷酸化
酶
聚合物
作者
M. Mutter,Adel Nefzi,Takuma Sato,Xicheng Sun,Franck Olivier Wahl,Torsten Wöhr
出处
期刊:PubMed
日期:1995-05-01
卷期号:8 (3): 145-53
被引量:71
摘要
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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