首页> 外文期刊>The FEBS journal >Functional analysis of a murine monoclonal antibody against the repetitive region of the fibronectin-binding adhesins fibronectin-binding protein A and fibronectin-binding protein B from Staphylococcus aureus
【24h】

Functional analysis of a murine monoclonal antibody against the repetitive region of the fibronectin-binding adhesins fibronectin-binding protein A and fibronectin-binding protein B from Staphylococcus aureus

机译:针对来自金黄色葡萄球菌的纤连蛋白结合黏附蛋白纤连蛋白结合蛋白A和纤连蛋白结合蛋白B的重复区的鼠单克隆抗体的功能分析

获取原文
获取原文并翻译 | 示例
           

摘要

Fibronectin-binding proteins A and B are multifunctional LPXTG staphylococcal adhesins, comprising an N-terminal region that binds fibrinogen and elastin, and a C-terminal domain that interacts with fibronectin. The C-terminal domain of fibronectin-binding protein A is organized into 11 tandem repeats, six of which bind the ligand with high affinity; other sites bind more weakly. Fibronectin-binding protein B has been postulated to harbor 10 rather than 11 repeats, but it contains the same number of high-affinity fibronectin-binding sites as fibronectin-binding protein A. In this study, we confirm this prediction and show that six of 10 sites bind with dissociation constants in the nanomolar range. We also found that the full-length repetitive region of fibronectin-binding protein B stimulated the production of a mAb (15E11) that binds with high affinity to an epitope shared by repeats 9 and 10 from both adhesins. With the use of truncated fragments of repeat 9 of fibronectin-binding protein A, we mapped the antibody epitope to the N-terminal segment and the fibronectin-binding site to the C-terminal segment of the repeat. The distinct localization of the 15E11 epitope and the fibronectin-binding site suggests that the interfering effect of the antibody might result from steric hindrance or a conformational change in the structure that reduces the accessibility of fibronectin to its binding determinant. The epitope is well exposed on the surface of staphylococcal cells, as determined by genetic analyses, fluorescence microscopy, and flow cytometry. When incubated with cells of Staphylococcs aureus strains, 15E11 inhibits attachment of bacteria to surface-coated fibronectin by almost 70%. Structured digital abstract: MINT-7991189, MINT-7991227, MINT-7991305, MINT-7991292, MINT-7991279, MINT-7991266, MINT-7991253, MINT-7991622: fnbA (uniprotkb: P14738) binds ( MI:0407) to Fibronectin (uniprotkb: P02751) by enzyme linked immunosorbent assay ( MI:0411) MINT-7991435, MINT-7991636, MINT-7991447, MINT-7991462, MINT-7991477, MINT-7991492, MINT-7991507, MINT-7991522: fnbA (uniprotkb: P14738) binds ( MI:0407) to Fibronectin (uniprotkb: P02751) by filter binding ( MI:0049) MINT-7991577, MINT-7991594: fnbB (uniprotkb: Q53682) binds ( MI:0407) to Fibronectin (uniprotkb: P02751) by surface plasmon resonance ( MI:0107) MINT-7991321, MINT-7991345, MINT-7991360, MINT-7991375, MINT-7991390, MINT-7991405, MINT-7991420: fnbB (uniprotkb: Q53682) binds ( MI:0407) to Fibronectin (uniprotkb: P02751) by filter binding ( MI:0049) MINT-7991103, MINT-7991114, MINT-7991126, MINT-7991138, MINT-7991153, MINT-7991165, MINT-7991177: fnbB (uniprotkb: Q53682) binds ( MI:0407) to Fibronectin (uniprotkb: P02751) by enzyme linked immunosorbent assay ( MI:0411) MINT-7991540, MINT-7991558: fnbA (uniprotkb: P14738) binds ( MI:0407) to Fibronectin (uniprotkb: P02751) by surface plasmon resonance ( MI:0107)
机译:纤连蛋白结合蛋白A和B是多功能LPXTG葡萄球菌粘附蛋白,其包含结合纤溶蛋白原和弹性蛋白的N端区域和与纤连蛋白相互作用的C端结构域。纤连蛋白结合蛋白A的C末端结构域组织成11个串联重复序列,其中6个以高亲和力与配体结合。其他站点绑定较弱。纤连蛋白结合蛋白B被假定具有10个重复序列,而不是11个重复序列,但它与纤连蛋白结合蛋白A包含相同数量的高亲和性纤连蛋白结合位点。在这项研究中,我们证实了这一预测并显示出6个10个位点与纳摩尔范围内的解离常数结合。我们还发现纤连蛋白结合蛋白B的全长重复区域刺激了mAb(15E11)的产生,该单克隆抗体以高亲和力与两个粘附素的重复序列9和10共享的表位结合。通过使用纤连蛋白结合蛋白A重复序列9的截短片段,我们将抗体表位定位于重复序列的N末端片段,将纤连蛋白结合位点定位于重复序列的C末端片段。 15E11表位和纤连蛋白结合位点的独特定位表明,抗体的干扰作用可能是由于空间障碍或结构构象变化所致,从而降低了纤连蛋白对其结合决定簇的可及性。通过遗传分析,荧光显微镜和流式细胞仪确定,该表位在葡萄球菌细胞表面上暴露良好。当与金黄色葡萄球菌菌株的细胞一起孵育时,15E11抑制细菌附着到表面包被的纤连蛋白上,几乎抑制了70%。结构化数字摘要:MINT-7991189,MINT-7991227,MINT-7991305,MINT-7991292,MINT-7991279,MINT-7991266,MINT-7991253,MINT-7991622:fnbA(uniprotkb:P14738)与纤连蛋白结合(MI:0407) (uniprotkb:P02751)通过酶联免疫吸附测定(MI:0411)MINT-7991435,MINT-7991636,MINT-7991447,MINT-7991462,MINT-7991477,MINT-7991492,MINT-7991507,MINT-7991522:fnbA(uniprotkb :P14738)通过过滤器结合(MI:0049)结合(MI:0407)与纤连蛋白(uniprotkb:P02751)MINT-7991577,MINT-7991594:fnbB(uniprotkb:Q53682)结合(MI:0407)与纤连蛋白(uniprotkb:P02751) )通过表面等离振子共振(MI:0107)MINT-7991321,MINT-7991345,MINT-7991360,MINT-7991375,MINT-7991390,MINT-7991405,MINT-7991420:fnbB(uniprotkb:Q53682)结合(MI:0407)通过过滤器结合(MI:0049)与纤连蛋白(uniprotkb:P02751)结合到MINT-7991103,MINT-7991114,MINT-7991126,MINT-7991138,MINT-7991153,MINT-7991165,MINT-7991177:fnbB(uniprotkb:Q53682)结合(MI:0407)到纤连蛋白(uniprotkb: P02751)通过酶联免疫吸附测定(MI:0411)MINT-7991540,MINT-7991558:fnbA(uniprotkb:P14738)通过表面等离振子共振(MI:0107)结合(MI:0407)与纤连蛋白(uniprotkb:P02751)

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号