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山东大学学报(理学版) ›› 2014, Vol. 49 ›› Issue (1): 31-35.doi: 10.6040/j.issn.1671-9352.0.2013.235

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多肽C端衍生物的反向固相合成新方法

陈雷,金枝,刘强,王明,王朴*   

  1. 山东大学药学院,山东 济南 250012
  • 收稿日期:2013-05-20 出版日期:2014-01-20 发布日期:2014-01-15
  • 通讯作者: 王朴(1955- ),男,教授,主要从事有机合成及多肽蛋白质合成研究.Email:puwang@sdu.edu.cn
  • 作者简介:陈雷(1987- ),男,硕士研究生,主要从事有机合成及多肽合成.Email:chenleijtgzh@163.com
  • 基金资助:

    国家自然科学基金资助项目(21072116);山东省自然科学基金资助项目(ZR2010BM040)

Novel synthesis of C-terminal polypeptides by ISPPS method

CHEN Lei, JIN Zhi, LIU Qiang, WANG Ming, WANG Pu*   

  1. School of Pharmaceutical Science, Shandong University, Jinan 250012, Shandong, China
  • Received:2013-05-20 Online:2014-01-20 Published:2014-01-15

摘要:

新设计了一种多肽C-端衍生物的合成方法。本方法结合了Fmoc-SPPS技术与TAEC技术的优点,室温反应,反应条件温和,易于监测,反应过程中所需采取的保护基最少,后处理简单高效,与正向固相合成互补,可高效地合成多种多肽以及多肽C-端衍生物。

关键词: TAEC, 多肽, C-端衍生物, 反向固相合成

Abstract:

A facile approach for the preparation of polypeptide C-terminal derivatives by inverse solid phase peptide synthesis (ISPPS) was developed. This novel method combines both advantages of Fmoc-SPPS and TAEC technology, utilizes fewer functional group protection steps. In addition, the reaction can be carried out at room temperature under mild conditions and be easily monitored, and the working-up is simple and efficient. This method is complementary to the direct solid phase peptide synthesis. Several polypeptides as well as their C-terminal derivatives were efficiently prepared by this novel ISPPS method.

Key words: inverse solid phase peptide synthesis (ISPPS), C-terminal derivatives, TAEC, polypeptide

中图分类号: 

  • O629.7
[1] 郭战胜,侯旭光,张军伟,李亮,张海涛,于海. 三种鲍腹足肌胶原多肽抗氧化性研究[J]. 山东大学学报(理学版), 2016, 51(11): 66-73.
[2] 金枝,胡乃峰,刘强,王朴*. Tbfmoc-蛋氨酸在泛素固相合成中的应用[J]. J4, 2011, 46(7): 21-25.
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