Journal article

Aqueous microwave-assisted solid-phase peptide synthesis using Fmoc strategy. III: Racemization studies and water-based synthesis of histidine-containing peptides

Keiko Hojo, Natsuki Shinozaki, Koushi Hidaka, Yuko Tsuda, Yoshinobu Fukumori, Hideki Ichikawa, John D Wade

AMINO ACIDS | SPRINGER WIEN | Published : 2014

Abstract

In this study, we describe the first aqueous microwave-assisted synthesis of histidine-containing peptides in high purity and with low racemization. We have previously shown the effectiveness of our synthesis methodology for peptides including difficult sequences using water-dispersible 9-fluorenylmethoxycarbonyl-amino acid nanoparticles. It is an organic solvent-free, environmentally friendly method for chemical peptide synthesis. Here, we studied the racemization of histidine during an aqueous-based coupling reaction with microwave irradiation. Under our microwave-assisted protocol using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride, the coupling reaction can be effici..

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Grants

Awarded by "Strategic Research Foundation" at Private Universities matching fund subsidy from the Japanese Ministry of Education, Culture, Sports Science and Technology


Funding Acknowledgements

We are grateful to Dr. Hajime Hibino and Prof. Yuji Nishiuchi (Peptide Institute, Japan) for valuable advice and providing Fmoc-His(MBom)-OH. This work supported by a "Strategic Research Foundation" at Private Universities matching fund subsidy from the Japanese Ministry of Education, Culture, Sports Science and Technology, 2012-2016 (S1201010) and "Takeda Science Foundation". Studies at the Florey Institute of Neuroscience and Mental Health were supported by the Victorian Government Operational Infrastructure Support Program.