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土拉弗朗西斯菌GroEL中的B细胞表位

B-cell epitopes in GroEL of Francisella tularensis.

作者信息

Lu Zhaohua, Rynkiewicz Michael J, Madico Guillermo, Li Sheng, Yang Chiou-Ying, Perkins Hillary M, Sompuram Seshi R, Kodela Vani, Liu Tong, Morris Timothy, Wang Daphne, Roche Marly I, Seaton Barbara A, Sharon Jacqueline

机构信息

Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, Massachusetts, United States of America.

Department of Physiology and Biophysics, Boston University School of Medicine, Boston, Massachusetts, United States of America.

出版信息

PLoS One. 2014 Jun 26;9(6):e99847. doi: 10.1371/journal.pone.0099847. eCollection 2014.

Abstract

The chaperonin protein GroEL, also known as heat shock protein 60 (Hsp60), is a prominent antigen in the human and mouse antibody response to the facultative intracellular bacterium Francisella tularensis (Ft), the causative agent of tularemia. In addition to its presumed cytoplasmic location, FtGroEL has been reported to be a potential component of the bacterial surface and to be released from the bacteria. In the current study, 13 IgG2a and one IgG3 mouse monoclonal antibodies (mAbs) specific for FtGroEL were classified into eleven unique groups based on shared VH-VL germline genes, and seven crossblocking profiles revealing at least three non-overlapping epitope areas in competition ELISA. In a mouse model of respiratory tularemia with the highly pathogenic Ft type A strain SchuS4, the Ab64 and N200 IgG2a mAbs, which block each other's binding to and are sensitive to the same two point mutations in FtGroEL, reduced bacterial burden indicating that they target protective GroEL B-cell epitopes. The Ab64 and N200 epitopes, as well as those of three other mAbs with different crossblocking profiles, Ab53, N3, and N30, were mapped by hydrogen/deuterium exchange-mass spectrometry (DXMS) and visualized on a homology model of FtGroEL. This model was further supported by its experimentally-validated computational docking to the X-ray crystal structures of Ab64 and Ab53 Fabs. The structural analysis and DXMS profiles of the Ab64 and N200 mAbs suggest that their protective effects may be due to induction or stabilization of a conformational change in FtGroEL.

摘要

伴侣蛋白GroEL,也被称为热休克蛋白60(Hsp60),是人和小鼠针对兼性胞内细菌土拉弗朗西斯菌(Ft)产生抗体反应中的一种重要抗原,土拉弗朗西斯菌是兔热病的病原体。除了推测其位于细胞质中,据报道FtGroEL还是细菌表面的一种潜在成分,并可从细菌中释放出来。在本研究中,基于共享的VH-VL种系基因,将13种针对FtGroEL的IgG2a和1种IgG3小鼠单克隆抗体(mAb)分为11个独特的组,并通过竞争ELISA法确定了7种交叉阻断谱,揭示了至少3个不重叠的表位区域。在由高致病性A型菌株SchuS4引起的呼吸道兔热病小鼠模型中,Ab64和N200 IgG2a mAb可相互阻断与FtGroEL的结合,并且对FtGroEL中的相同两个点突变敏感,它们可降低细菌载量,这表明它们靶向保护性GroEL B细胞表位。通过氢/氘交换质谱法(DXMS)对Ab64和N200表位以及其他三种具有不同交叉阻断谱的mAb(Ab53、N3和N30)的表位进行了定位,并在FtGroEL的同源模型上进行了可视化展示。该模型通过与Ab64和Ab53 Fab的X射线晶体结构进行实验验证的计算对接得到了进一步支持。Ab64和N200 mAb的结构分析和DXMS谱表明,它们的保护作用可能是由于诱导或稳定了FtGroEL的构象变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5677/4072690/dd3e8c77f5e9/pone.0099847.g001.jpg

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