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一种靶向载脂蛋白B100和胆固醇酯转运蛋白的植物源免疫原性蛋白的制备:迈向基于植物的动脉粥样硬化疫苗

Production of a plant-derived immunogenic protein targeting ApoB100 and CETP: toward a plant-based atherosclerosis vaccine.

作者信息

Salazar-Gonzalez Jorge Alberto, Rosales-Mendoza Sergio, Romero-Maldonado Andrea, Monreal-Escalante Elizabeth, Uresti-Rivera Edith Elena, Bañuelos-Hernández Bernardo

机构信息

Laboratorio de Biofarmacéuticos Recombinantes, Facultad de Ciencias Químicas, Universidad Autónoma de San Luis Potosí, Av. Dr. Manuel Nava 6, 78210, San Luis Potosí, SLP, Mexico.

出版信息

Mol Biotechnol. 2014 Dec;56(12):1133-42. doi: 10.1007/s12033-014-9793-6.

Abstract

In an effort to initiate the development of a plant-based vaccination model against atherosclerosis, a cholera toxin B subunit (CTB)-based chimeric protein was designed to target both ApoB100 and CETP epitopes associated with immunotherapeutic effects in atherosclerosis. Epitopes were fused at the C-terminus of CTB to yield a protein called CTB:p210:CETPe. A synthetic gene coding for CTB:p210:CETPe was successfully transferred to tobacco plants with no phenotypic alterations. Plant-derived CTB:p210:CETPe was expressed and assembled in the pentameric form. This protein retained the target antigenic determinants, as revealed by GM1-ELISA and Western blot analyses. Higher expresser lines reached recombinant protein accumulation levels up to 10 µg/g fresh weight in leaf tissues and these lines carry a single insertion of the transgene as determined by qPCR. Moreover, when subcutaneously administered, the biomass from these CTB:p210:CETPe-producing plants was able to elicit humoral responses in mice against both ApoB100 and CETP epitopes and human serum proteins. These findings evidenced for the first time that atherosclerosis-related epitopes can be expressed in plants retaining immunogenicity, which opens a new path in the molecular farming field for the development of vaccines against atherosclerosis.

摘要

为了启动针对动脉粥样硬化的植物源疫苗接种模型的开发,设计了一种基于霍乱毒素B亚基(CTB)的嵌合蛋白,以靶向与动脉粥样硬化免疫治疗效果相关的载脂蛋白B100(ApoB100)和胆固醇酯转运蛋白(CETP)表位。表位在CTB的C末端融合,产生一种名为CTB:p210:CETPe的蛋白。编码CTB:p210:CETPe的合成基因成功转移到烟草植物中,且无表型改变。植物源CTB:p210:CETPe以五聚体形式表达和组装。GM1-ELISA和蛋白质印迹分析表明,该蛋白保留了目标抗原决定簇。高表达系在叶片组织中的重组蛋白积累水平达到每克鲜重10微克,通过定量聚合酶链反应(qPCR)确定这些系携带单个转基因插入。此外,当皮下给药时,这些产生CTB:p210:CETPe的植物的生物量能够在小鼠体内引发针对ApoB100和CETP表位以及人血清蛋白的体液反应。这些发现首次证明与动脉粥样硬化相关的表位可以在保持免疫原性的植物中表达,这为分子农业领域开发抗动脉粥样硬化疫苗开辟了一条新途径。

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