High efficiency synthesis of insulin by self-assembly based organic chemistry

08/05/2018 Osaka University

Researchers at Tokai University, Osaka University, Tohoku University and Fukuoka University report in the journal Communications Chemistry on the synthesis of insulin based on the self-assembly of polypeptide chains at about 40% efficiency. This new approach is expected to enable flexibility in synthesizing order made insulin compounds that cannot be produced using conventional biological approaches based on genetic engineering.

Insulin is a hormone that acts to lower the rise in blood glucose level after meals and is used as a therapeutic agent for diabetes. Since insulin has a characteristic molecular structure in which two peptide chains (A and B chains) are connected by two disulfide bridges (SS bonds), chemical synthesis has been considered as being difficult achieve. Currently, insulin is manufactured by a genetic engineering process.

Here, Michio Iwaoka at Tokai University, Japan, in collaboration with the groups of Hironobu Hojo at Osaka University and Kenji Inaba at Tohoku University, and Setsuko Ando at Fukuoka University, report on their success in efficiently synthesizing insulin by using only chemical processes based on organic synthesis.

The researchers have previously reported on the efficient chemical synthesis of insulin (seleno-insulin) in which selenocysteine was substituted for insulin containing cysteine to replace the SS bond between the peptide chains with a diselenide crosslink (SeSe bond).

In this paper, the researchers have improved on the previous synthesis method of seleno-insulin and produced natural insulin (bovine insulin) at a higher yield (of approximately 40%) than seleno-insulin. Furthermore, by applying this new method, they succeeded in the efficient chemical synthesis of insulin families such as human insulin and human type 2 relaxin.

In this research, the group first examined the process (folding pathway) by which insulin A chain and insulin B chain combine to form the structure of natural type insulin. Then, based on the pathway, they succeeded in optimizing folding conditions of bovine insulin and obtaining bovine insulin at high yield of about 40%.

The advantages of this synthesis method is that it does not require any large-scale production equipment because it does not use any genetic engineering technique and insulin can be produced by the simple process of mixing A chain and B chain—both of which can be synthesized by a solid phase peptide synthesis method using a resin.

“Using this ‘self-assembly’ approach it would be possible to modify the structure of insulin, such as introducing an unnatural amino acid into insulin,” explains Iwaoka. “We expect that this method could be applied to the development of many types of insulin preparations such as long-acting and super quick-acting types.”

Full bibliographic information


Reference Kenta Arai, Toshiki Takei, Reina Shinozaki, Masato Noguchi, Shouta Fujisawa, Hidekazu Katayama, Luis Moroder, Setsuko Ando, Masaki Okumura, Kenji Inaba, Hironobu Hojo & Michio Iwaoka. Characterization and optimization of two-chain folding pathways of insulin via native chain assembly. Communications Chemistry. DOI: 10.1038/s42004-018-0024-0 This work was supported by KAKENHI Grant Number 26888016 for Research Activity Start-up (to K.A.), in part by Research and Study Project of Tokai University, Educational System General Research Organization (to K.A. and M.I.), Collaborative Research Program of Institute for Protein Research, Osaka University CR-15-01 (M.I. and H.H.), and Coop-erative Research Program of Network Joint Research Center for Material and Devices (M. I. and K.I.).
Attached files
  • Fig1. A simple protocol developed for insulin preparation. (132)

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