Institute of Pharmacology and Toxicology, University of Ulm Medical Center, Albert-Einstein-Allee 11, 89081 Ulm, Germany.
Toxicon. 2013 Dec 1;75:144-7. doi: 10.1016/j.toxicon.2013.02.002. Epub 2013 Feb 16.
We demonstrated previously that monocytes and macrophages are target cells for the Rho-modifying Clostridium botulinum C3 ADP-ribosyltransferase. Here, we report the construction, expression and characterization of a recombinant streptavidin-C3 fusion protein which allows for delivery of biotin-labelled molecules into the cytosol of macrophages via enzymatically inactive C3bot1E174Q. The enzyme domain of diphtheria toxin was used as cargo to demonstrate proof of principle. This transport system could represent an attractive tool for experimental monocyte/macrophage pharmacology.
我们之前已经证明,单核细胞和巨噬细胞是梭菌 C3 ADP-核糖基转移酶的靶细胞。在这里,我们报告了一种重组链霉亲和素-C3 融合蛋白的构建、表达和特性,该融合蛋白允许通过酶失活的 C3bot1E174Q 将生物素标记的分子递送到巨噬细胞的细胞质中。白喉毒素的酶结构域被用作货物来证明原理的可行性。该运输系统可能代表用于实验性单核细胞/巨噬细胞药理学的有吸引力的工具。