Brakstad O G, Maeland J A
Department of Microbiology, Faculty of Medicine, University of Trondheim, Norway.
APMIS. 1989 Feb;97(2):166-74.
Monoclonal antibodies (MAbs) against Staphylococcus aureus thermonuclease (TN) were raised by immunizing BALB/c mice with a commercial TN preparation. Six monoclones were generated producing MAbs specific for S. aureus TN as tested in Western blots and ELISA. They all combined with a 17 kD and a 21 kD protein, respectively, both of which showed DNase activity. All MAbs were of IgG1 isotype with kappa light chain. Competition ELISA showed that five of the MAbs recognized a total of three different binding sites of TN, designated I, II and III, respectively. Only the anti-site II MAbs inhibited the DNase activity. A MAb-based sandwich ELISA showed a lower detection limit for TN of approximately 0.5 ng/ml protein. Only S. aureus strains (culture supernatants) showed positive ELISA (31 positive/31 tested), although other tested gram positive cocci produced thermostable nucleases. The MAbs have potentials as reagents for rapid and specific detection of S. aureus.
用市售的金黄色葡萄球菌耐热核酸酶(TN)制剂免疫BALB/c小鼠,制备了抗金黄色葡萄球菌耐热核酸酶(TN)的单克隆抗体(MAb)。通过蛋白质印迹法和酶联免疫吸附测定(ELISA)检测,产生了6个单克隆,其产生的单克隆抗体对金黄色葡萄球菌TN具有特异性。它们分别与一个17kD和一个21kD的蛋白质结合,这两种蛋白质均显示出脱氧核糖核酸酶(DNase)活性。所有单克隆抗体均为κ轻链的IgG1同种型。竞争ELISA表明,其中5个单克隆抗体总共识别TN的3个不同结合位点,分别命名为I、II和III。只有抗位点II的单克隆抗体抑制DNase活性。基于单克隆抗体的夹心ELISA显示,TN的检测下限约为0.5ng/ml蛋白质。尽管其他测试的革兰氏阳性球菌产生耐热核酸酶,但只有金黄色葡萄球菌菌株(培养上清液)的ELISA呈阳性(31个测试样本中有31个阳性)。这些单克隆抗体有潜力作为快速、特异性检测金黄色葡萄球菌的试剂。