Flock J I, Fröman G, Jönsson K, Guss B, Signäs C, Nilsson B, Raucci G, Höök M, Wadström T, Lindberg M
Department of Microbiology, University of Uppsala, Sweden.
EMBO J. 1987 Aug;6(8):2351-7. doi: 10.1002/j.1460-2075.1987.tb02511.x.
The gene encoding the fibronectin-binding protein (FNBP) from Staphylococcus aureus strain 8325-4 was isolated from a gene bank in pBR322. The original clone, containing a 6.5-kb insert, gave a functional product present in the periplasm of Escherichia coli. Analysis of polypeptides isolated after affinity chromatography on fibronectin-Sepharose followed by ion-exchange chromatography revealed two gene products, 87 and 165 kd in mol. wt. The amino acid compositions of these two polypeptides and a native FNBP from S. aureus strain Newman were very similar. Antibodies raised against the native FNBP from strain Newman precipitated the 125I-labelled 165-kd polypeptide, and unlabeled 165- and 87-kd polypeptides as well as native FNBP inhibited the immunoprecipitation reactions. The region of the fnbp-gene encoding the fibronectin-binding activity has been identified and subcloned in an expression vector based on the staphylococcal protein A gene. The resulting product in E. coli is an extracellular fusion protein consisting of two IgG-binding domains of protein A followed by a fibronectin-binding region. The fusion protein binds to fibronectin and completely inhibits the binding of fibronectin to intact cells of S. aureus.
从金黄色葡萄球菌8325 - 4株中编码纤连蛋白结合蛋白(FNBP)的基因,是从pBR322中的基因文库中分离得到的。最初的克隆含有一个6.5 kb的插入片段,其在大肠杆菌周质中产生了一种功能性产物。对在纤连蛋白-琼脂糖亲和层析后再经离子交换层析分离得到的多肽进行分析,发现了两种基因产物,分子量分别为87 kd和165 kd。这两种多肽以及金黄色葡萄球菌纽曼菌株的天然FNBP的氨基酸组成非常相似。针对纽曼菌株天然FNBP产生的抗体沉淀了125I标记的165 kd多肽,未标记的165 kd和87 kd多肽以及天然FNBP也抑制了免疫沉淀反应。已鉴定出fnbp基因中编码纤连蛋白结合活性的区域,并将其亚克隆到基于葡萄球菌蛋白A基因的表达载体中。在大肠杆菌中产生的产物是一种细胞外融合蛋白,由蛋白A的两个IgG结合结构域和一个纤连蛋白结合区域组成。该融合蛋白能与纤连蛋白结合,并完全抑制纤连蛋白与金黄色葡萄球菌完整细胞的结合。