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Monoclonal Antibody That Blocks the Toll-Like Receptor 5 Binding Region of Flagellin

机译:阻断鞭毛蛋白Toll样受体5结合区的单克隆抗体

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摘要

The conserved domain of bacteria-derived flagellin coupling Toll-like receptor 5 (TLR5) activates NF-κB and MAPK signaling transductions, which subsequently regulate the transcription and expression of genes encoding immune mediators. However, whether the flagellin binding monoclonal antibody (MAb) obstructs TLR5-associated signaling is unclear. Here we report on the production and characterization of MAb 5G10 that specifically recognizes flagellin. The MAb 5G10 was produced by the hybridization of mouse myeloma cell SP2/0 with splenocyte from a flagellin immunized BALB/c mouse. We observed that deletion of the conserved amino acid residues 89-96 made flagellin lose its capacity for binding 5G10. Additionally, MAb 5G10 remarkably suppressed the expression of cytokine IL8 of Caco-2 cell by blocking the flagellin-TLR5 signaling. Furthermore, this MAb would be useful for cytosolic localization of flagellin and would facilitate the elucidation of the physiological function of specific pathogen-associated molecular patterns.
机译:细菌来源的鞭毛蛋白偶联的Toll样受体5(TLR5)的保守结构域激活NF-κB和MAPK信号转导,随后调节编码免疫介质的基因的转录和表达。但是,鞭毛蛋白结合单克隆抗体(MAb)是否会阻碍TLR5相关的信号传导尚不清楚。在这里,我们报告了特异性识别鞭毛蛋白的MAb 5G10的生产和表征。通过将小鼠骨髓瘤细胞SP2 / 0与来自鞭毛蛋白免疫的BALB / c小鼠的脾细胞杂交来生产MAb 5G10。我们观察到保守氨基酸残基89-96的缺失使鞭毛蛋白丧失了其结合5G10的能力。另外,MAb 5G10通过阻断鞭毛蛋白-TLR5信号传导显着抑制Caco-2细胞的细胞因子IL8的表达。此外,该MAb可用于鞭毛蛋白的胞质定位,并有助于阐明特定病原体相关分子模式的生理功能。

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