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Recent developments in peptide ligation independent of amino acid side-chain functional group

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  • ReceivedFeb 8, 2017
  • AcceptedApr 13, 2017
  • PublishedJul 4, 2017

Abstract

Chemical synthesis of peptides and proteins has evolved into an indispensable tool for chemical biology. Peptide ligation is a straightforward technique for joining two short peptide fragments together via a native peptide bond to afford a larger natural peptide or protein. However, the junction sites are limited to several specific amino acids because most peptide ligations involve participation of the side-chain functional groups of the junction-site amino acids. To overcome such intrinsic limitations, “general” peptide ligations which do not rely on the side-chain functional group have been developed. This review summarized the recent developments in peptide ligations that are independent of side-chain functional group of ligation-junction-site amino acid.


Funded by

National Natural Science Foundation of China(21462023)

Natural Science Foundation of Jiangxi Province(20143ACB20007,20153BCB23018)


Acknowledgment

This work was supported by the National Natural Science Foundation of China (21462023), and the Natural Science Foundation of Jiangxi Province (20143ACB20007, 20153BCB23018).


Interest statement

The authors declare that they have no conflict of interest.


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