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Chemical protein synthesis allows the construction of well-defined structural variations and facilitates the development of deeper understanding of protein structure-function relationships and new protein engineering strategies. Herein, we report the chemical synthesis of interleukin-2 (IL-2) variants on a multimilligram scale and the formation of non-natural disulfide mimetics that improve stability against reduction. The synthesis was accomplished by convergent KAHA ligations; the acidic conditions of KAHA ligation proved to be valuable for the solubilization of the hydrophobic segments of IL-2. The bioactivity of the synthetic IL-2 and its analogues were shown to be equipotent to recombinant IL-2 and exhibit improved stability against reducing agents. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Citation

Claudia E Murar, Mamiko Ninomiya, Satomi Shimura, Ufuk Karakus, Onur Boyman, Jeffrey W Bode. Chemical Synthesis of Interleukin-2 and Disulfide Stabilizing Analogues. Angewandte Chemie (International ed. in English). 2020 May 25;59(22):8425-8429

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PMID: 32032465

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