大肠杆菌热稳定型肠毒素的结构表征

I. Matečko, Bjoern Burmann, K. Schweimer, H. Kalbacher, J. Einsiedel, P. Gmeiner, P. Rösch
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引用次数: 7

摘要

大肠杆菌热稳定型肠毒素STa是膜鸟苷酸环化酶C的激动剂,其内源性配体是肽激素观音苷和尿观音苷。然而这些肽只包含两个二硫键,STa通过一个额外的二硫键桥来稳定。我们化学合成了源自人类大肠杆菌菌株的肠毒素STh,并通过核磁共振谱和分子动力学计算确定了其结构和动力学。化学合成显然证明是成功的,并导致天然二硫键的形成。内源性配体观音林和尿观音林表现出与肠毒素相同的总体结构特征和动力学特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural Characterisation of the E. coli Heat Stable Enterotoxin STh
E. coli heat stable enterotoxin STa is an agonist of the membrane guanylate cyclase C whose endogenous ligands are the peptide hormones guanylin and uroguanylin. Whereas these peptides contain only two disulfide bonds, STa is stabilized by one additional disulfide bridge. We chemically synthesized the enterotoxin STh that originates from the E. coli strain found in humans, and we determined its structure and its dynamics by nuclear magnetic resonance spec- troscopy and molecular dynamics calculations. Chemical synthesis clearly proved successful and resulted in the formation of the native disulfide bonds. The endogenous ligands guanylin and uroguanylin show the same general structural features and dynamics properties as the enterotoxin.
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