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Efficient synthesis of trypsin inhibitor SFTI-1 via intramolecular ligation of peptide hydrazide
Authors:Yi-Qun Chen  Chen-Chen Chen  Yao He  Mu Yu  Lin Xu  Chang-lin Tian  Qing-Xiang Guo  Jing Shi  Min Zhang  Yi-Ming Li
Affiliation:1. School of Life Science, Anhui University, Hefei, Anhui 230601, China;2. School of Medical Engineering, School of Chemical Engineering, Hefei University of Technology, Hefei, Anhui 230009, China;3. China High Magnetic Field Laboratory, Chinese Academy of Sciences, School of Life Sciences, University of Science and Technology of China, Hefei 230026, China;4. Department of Chemistry, University of Science and Technology of China, Hefei 230026, China
Abstract:Cyclic peptide trypsin inhibitor SFTI-1 was synthesized via intramolecular ligation of a linear peptide hydrazide with high yield. This cyclization strategy did not cause epimerization at the C-terminal Arg residue. CD spectrum and NMR spectroscopy analysis demonstrated that well-folded SFTI-1 could be obtained via standard oxidative folding process. Thus, we present a simple and cost-efficient strategy for the synthesis of SFTI-1.
Keywords:Cyclic peptides   Protein chemical synthesis     boldFont"  >SFTI-1   Peptide hydrazides
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