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Novel immunotoxin: A fusion protein consisting of gelonin and an acetylcholine receptor fragment as a potential immunotherapeutic agent for the treatment of Myasthenia gravis

机译:新型免疫毒素:由明胶和乙酰胆碱受体片段组成的融合蛋白,可作为重症肌无力的潜在免疫治疗剂

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In continuation of our attempts for antigen-specific suppression of the immune system [I.L. Urbatsch, R.K.M. Sterz, K. Peper, W.E. Trommer, Eur. J. Immunol. 23(1993) 776-779] a novel fusion protein composed of amino acids 4-181 of the extracellular domain of the alpha-subunit of the human muscle acetylcholine receptor and the plant toxin gelonin was expressed in Escherichia coli. The fusion protein formed inclusion bodies but could be solubilized in the presence of guanidinium hydrochloride. After a simple two step purification and refolding procedure, it exhibited a native structure at least in the main immunogenic region as shown by antibodies recognizing a conformational epitope. Half maximal inhibition of translation was achieved at 46 ng/ml as compared to 4.6 ng/ml for native and 2.4 for recombinant gelonin. Its use as therapeutic agent for the treatment of Myasthenia gravis was investigated in an animal model. Female Lewis rats were immunized with complete acetylcholine receptor from the electric ray Torpedo californica and developed thereafter experimental autoimmune M. gravis. Quantitative assessment of the disease was achieved by repetitive stimulation of the Nervus tibialis. Rats showed no symptoms of M. gravis, neither visually nor electrophysiologically after treatment with the fusion protein as determined one and seven weeks after the second application. This approach may also be useful for the therapy of further autoimmune diseases by substituting other autoantigens for the AchR fragment in the fusion protein. (c) 2005 Elsevier Inc. All rights reserved.
机译:继续我们对免疫系统进行抗原特异性抑制的尝试[I.L.英国Urbatsch斯特兹(W.E.)特罗默J.免疫。 [J.Am.Chem.Soc.23(1993)776-779]在大肠杆菌中表达了由人肌肉乙酰胆碱受体的α-亚基的胞外域的氨基酸4-181和植物毒素gelonin组成的新型融合蛋白。融合蛋白形成包涵体,但可以在盐酸胍存在下溶解。经过简单的两步纯化和重折叠程序后,它至少在主要免疫原性区域表现出天然结构,如识别构象表位的抗体所示。相对于天然胶凝蛋白为4.6 ng / ml和重组胶凝蛋白为2.4 ng / ml,翻译的最大抑制作用达到了46 ng / ml的一半。在动物模型中研究了其作为治疗重症肌无力的治疗剂的用途。用来自加州电鱼雷的完全乙酰胆碱受体免疫雌性Lewis大鼠,然后进行实验性自身免疫性重症莫拉氏菌的培养。通过重复刺激胫神经来实现对该疾病的定量评估。在第二次施用后一星期和七周确定,用融合蛋白处理后,大鼠在视觉和电生理上均未显示出重症分支杆菌的症状。通过用其他自身抗原替代融合蛋白中的AchR片段,该方法还可用于进一步的自身免疫性疾病的治疗。 (c)2005 Elsevier Inc.保留所有权利。

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