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通过结合多肽表达和化学活化的方法高效合成多肽-α-硫酯,用于半合成具有寡糖的干扰素-γ。

Efficient synthesis of polypeptide-α-thioester by the method combining polypeptide expression and chemical activation for the semi-synthesis of interferon-γ having oligosaccharides.

作者信息

Kajihara Yasuhiro, Kanemitsu Yurie, Nishihara Mika, Okamoto Ryo, Izumi Masayuki

机构信息

Department of chemistry, Osaka University, 1-1, Machikaneyama, Toyonaka, 560-0043, Japan.

出版信息

J Pept Sci. 2014 Dec;20(12):958-63. doi: 10.1002/psc.2709. Epub 2014 Nov 6.

Abstract

In order to synthesize interferon-γ glycoform having an oligosaccharide at the 97 position by a semi-synthetic method, interferon-γ-polypeptide-(1-94)-α-hydrazide was prepared by the specific Cys-cyanylation of polypeptide-(1-94)-Cys-His6 expressed from E. coli and subsequent hydrazinolysis in 22% yield (two steps). This polypeptide-α-hydrazide was then converted into corresponding polypeptide-α-thioester under NaNO2 /acid conditions followed by thiolysis in 83% yield.

摘要

为了通过半合成方法合成在97位具有寡糖的干扰素-γ糖型,通过对大肠杆菌表达的多肽-(1-94)-Cys-His6进行特定的半胱氨酸氰化以及随后的肼解反应,以22%的产率(两步)制备了干扰素-γ-多肽-(1-94)-α-酰肼。然后在亚硝酸钠/酸条件下将该多肽-α-酰肼转化为相应的多肽-α-硫酯,随后进行硫解反应,产率为83%。

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