4.1 Article

A shelf stable Fmoc hydrazine resin for the synthesis of peptide hydrazides

期刊

PEPTIDE SCIENCE
卷 114, 期 5, 页码 -

出版社

WILEY
DOI: 10.1002/pep2.24268

关键词

Fmoc resins; native chemical ligation; peptide hydrazides; peptide thioesters; solid phase peptide synthesis

资金

  1. National Institutes of Health [R21GM132787]

向作者/读者索取更多资源

This study presents a practical method for the synthesis of C-terminal hydrazide peptides. By utilizing specific resin linkers, peptides containing 40 amino acids were successfully synthesized, demonstrating the broad applicability of this method.
C-terminal hydrazides are an important class of synthetic peptides with an ever expanding scope of applications, but their widespread application for chemical protein synthesis has been hampered due to the lack of stable resin linkers for synthesis of longer and more challenging peptide hydrazide fragments. We present a practical method for the regeneration, loading, and storage of trityl-chloride resins for the production of hydrazide containing peptides, leveraging 9-fluorenylmethyl carbazate. We show that these resins are extremely stable under several common resin storage conditions. The application of these resins to solid phase peptide synthesis (SPPS) is demonstrated through the synthesis of the 40-mer GLP-1R agonist peptide P5. These studies support the broad utility of Fmoc-NHNH-Trt resins for SPPS of C-terminal hydrazide peptides.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.1
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据