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在体外烟草细胞中表达的前蓖麻毒蛋白经过了充分加工且具有生物活性。

Preproricin expressed in Nicotiana tabacum cells in vitro is fully processed and biologically active.

作者信息

Tagge E P, Chandler J, Harris B, Czako M, Marton L, Willingham M C, Burbage C, Afrin L, Frankel A E

机构信息

Department of Surgery, Medical University of South Carolina, Charleston, South Carolina, 29425, USA.

出版信息

Protein Expr Purif. 1996 Aug;8(1):109-18. doi: 10.1006/prep.1996.0080.

Abstract

Ricin, the highly toxic glycoprotein expressed in the endosperm of castor seeds, is composed of a galactose-binding lectin B chain (RTB) disulfide linked to a RNA N-glycosidase A chain (RTA). Chemically modified ricin has been conjugated to monoclonal antibodies and used for targeted therapy of cancer and autoimmune diseases. Replacement of chemically coupled molecules with a genetically engineered targeted ricin would improve homogeneity and yield and permit structural changes in the fusion toxin to be introduced readily by oligonucleotide-directed mutagenesis. Previous methods of expression of ricin fusion proteins have been limited to expression of RTA or RTB moieties alone or expression of incompletely processed toxin in Xenopus laevis oocytes. In the present study, we introduced the cDNA encoding preproricin into cultured tobacco cells via Agrobacterium tumefaciens-mediated gene transfer. Yields of ricin in soluble cell extracts were 1 microg/g in cells or, approximately, 0.1% of the total soluble protein. The ricin was partially purified by P2 monoclonal antibody anti-RTB affinity chromatography. The RTA and RTB immunoreactive material migrated on SDS-PAGE at 65 kDa under nonreducing conditions and at 32-35 kDa under reducing conditions. The tobacco ricin bound to immobilized asialofetuin as avidly as castor bean ricin, suggesting intact sugar binding. Tobacco ricin inhibited rabbit reticulocyte lysate protein translation similar to castor bean ricin (IC50 of 3 x 10(-12) M for tobacco ricin and 1 x 10(-11) M for castor bean ricin). The human cutaneous T cell lymphoma cell line HUT102 showed similar sensitivity to tobacco ricin when compared to castor bean ricin (IC50 = 9 x 10(-13) and 2 x 10(-12) M, respectively). The efficiency of gene transfer, reasonable levels of expression, and full post-translational processing indicate that this expression system is suitable for production of ricin fusion toxins for therapeutic applications.

摘要

蓖麻毒素是一种在蓖麻籽胚乳中表达的剧毒糖蛋白,由与RNA N - 糖苷酶A链(RTA)通过二硫键相连的半乳糖结合凝集素B链(RTB)组成。化学修饰的蓖麻毒素已与单克隆抗体偶联,并用于癌症和自身免疫性疾病的靶向治疗。用基因工程靶向蓖麻毒素替代化学偶联分子将提高均一性和产量,并允许通过寡核苷酸定向诱变轻松引入融合毒素的结构变化。以前表达蓖麻毒素融合蛋白的方法仅限于单独表达RTA或RTB部分,或在非洲爪蟾卵母细胞中表达未完全加工的毒素。在本研究中,我们通过根癌农杆菌介导的基因转移将编码前蓖麻毒素的cDNA导入培养的烟草细胞中。可溶性细胞提取物中蓖麻毒素的产量在细胞中为1微克/克,约占总可溶性蛋白的0.1%。蓖麻毒素通过P2抗RTB单克隆抗体亲和层析进行部分纯化。在非还原条件下,RTA和RTB免疫反应性物质在SDS - PAGE上迁移至65 kDa,在还原条件下迁移至32 - 35 kDa。烟草蓖麻毒素与固定化的去唾液酸胎球蛋白的结合与蓖麻籽蓖麻毒素一样 avidly,表明糖结合完整。烟草蓖麻毒素抑制兔网织红细胞裂解物蛋白翻译的效果与蓖麻籽蓖麻毒素相似(烟草蓖麻毒素的IC50为3×10(-12)M,蓖麻籽蓖麻毒素的IC50为1×10(-11)M)。与蓖麻籽蓖麻毒素相比,人皮肤T细胞淋巴瘤细胞系HUT102对烟草蓖麻毒素表现出相似的敏感性(IC50分别为9×10(-13)和2×10(-12)M)。基因转移效率、合理的表达水平和完整的翻译后加工表明该表达系统适用于生产用于治疗应用的蓖麻毒素融合毒素。 (注:avidly 这个词原文有误,应该是avidly,表示“贪婪地、强烈地”,这里结合语境推测是想说结合能力强,翻译为“同样强烈地” )

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