Orthogonal Cysteine鈥揚enicillamine Disulfide Pairing for Directing the Oxidative Folding of Peptides

详细信息    查看全文

• 作者：Yiwu Zheng ; Linxiang Zhai ; Yibing Zhao ; Chuanliu Wu
• 刊名：Journal of the American Chemical Society
• 出版年：2015
• 出版时间：December 9, 2015
• 年：2015
• 卷：137
• 期：48
• 页码：15094-15097
• 全文大小：313K
• ISSN：1520-5126

文摘

Precise disulfide pairing in synthetic peptides usually is achieved using orthogonal protecting group strategies or relies on primary sequence manipulation. Orthogonal disulfide pairing technology should be promising for directing the rational folding of multicyclic peptides from the fully reduced peptides. Here, we report a discovery on the orthogonality between heterodisulfide pairing of cysteine (Cys) and penicillamine (Pen) and formation of Cys-Cys/Pen-Pen homodisulfides. The orthogonal Cys-Pen disulfide pairing can be exploited for highly selective production of certain (multi)cyclic structures (or even a sole structure without isomers) through direct oxidation in air or thiol鈥揹isulfide exchanges in redox media. This strategy makes rational folding of multicyclic peptides without protecting groups, sequence manipulation, and complex synthetic reactions a reality, thus providing invaluable assets to peptide communities, and should greatly benefit the development of multicyclic peptide therapeutics and ligands.