Institute of Organic Chemistry III, Macromolecular Chemistry, University of Ulm , Albert-Einstein-Allee 11, D-89081 Ulm, Germany.
J Am Chem Soc. 2013 Nov 20;135(46):17254-7. doi: 10.1021/ja4084122. Epub 2013 Nov 7.
A facile, noncovalent solid-phase immobilization platform is described to assemble Janus-like supramolecular fusion proteins that are responsive to external stimuli. A chemically postmodified transporter protein, DHSA, is fused with (imino)biotinylated cargo proteins via an avidin adaptor with a high degree of spatial control. Notably, the derived heterofusion proteins are able to cross cellular membranes, dissociate at acidic pH due to the iminobiotin linker and preserve the enzymatic activity of the cargo proteins β-galactosidase and the enzymatic subunit of Clostridium botulinum C2 toxin. The mix-and-match strategy described herein opens unique opportunities to access macromolecular architectures of high structural definition and biological activity, thus complementing protein ligation and recombinant protein expression techniques.
描述了一种简便的非共价固相固定化平台,用于组装对外部刺激有响应的类 Janus 超分子融合蛋白。通过带有高空间控制度的亲和素接头,将化学后修饰的转运蛋白 DHSA 与(亚氨)生物素化的货物蛋白(如β-半乳糖苷酶和肉毒梭菌 C2 毒素的酶亚基)融合。值得注意的是,所得的杂合融合蛋白能够穿过细胞膜,由于亚氨生物素连接物在酸性 pH 下解离,并保持货物蛋白的酶活性β-半乳糖苷酶和肉毒梭菌 C2 毒素的酶亚基。本文所述的“混合搭配”策略为获得具有高结构定义和生物活性的大分子结构提供了独特的机会,从而补充了蛋白质连接和重组蛋白表达技术。
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