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首页> 外文期刊>Molecular Immunology >Humanization of an anti-human TNF-alpha antibody by variable region resurfacing with the aid of molecular modeling.
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Humanization of an anti-human TNF-alpha antibody by variable region resurfacing with the aid of molecular modeling.

机译:抗人TNF-α抗体的人源化是借助分子模型在可变区表面重铺。

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摘要

The murine monoclonal antibody Z12 is of therapeutic interest for its neutralizing biological activity against human tumor necrosis factor-alpha (hTNF-alpha). We attempted to humanize Z12 with variable domain resurfacing guided by computer modeling. First, the genes of heavy and light chain variable region (VH, VL) of Z12 were cloned and the whole three-dimensional structure of Fv fragment was constructed by using homology-based modeling and molecular docking methods. Then the complex model of Fv interacting with hTNF-alpha whose crystal structure derived from PDB database was gained with computer-guided docking program. Based on this model, a humanized version was designed. The humanized Fab antibody was constructed, expressed and purified in the pComb3H vector system and it showed unaltered binding affinity to the antigen as determined by ELISA and atomic force microscopy (AFM). The method described here can be used to humanize other anti-hTNF-alpha antibodies.
机译:鼠单克隆抗体Z12具有中和针对人类肿瘤坏死因子-α(hTNF-α)的生物活性的治疗价值。我们尝试通过计算机建模指导的可变域重铺来人性化Z12。首先,克隆了Z12的重链和轻链可变区(VH,VL)基因,并使用基于同源性的建模和分子对接方法构建了Fv片段的整个三维结构。然后用计算机指导的对接程序获得了Fv与hTNF-α相互作用的复杂模型,该模型的晶体结构来源于PDB数据库。基于此模型,设计了人性化版本。人源化Fab抗体在pComb3H载体系统中构建,表达和纯化,通过ELISA和原子力显微镜(AFM)测定,与抗原的结合亲和力未改变。此处描述的方法可用于使其他抗hTNF-α抗体人源化。

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