Hansen Debra T, Craciunescu Felicia M, Fromme Petra, Johnston Stephen A, Sykes Kathryn F
Biodesign Center for Applied Structural Discovery, Arizona State University, Tempe, Arizona.
Biodesign Center for Innovations in Medicine, Arizona State University, Tempe, Arizona.
Curr Protoc Protein Sci. 2018 Feb 21;91:29.20.1-29.20.22. doi: 10.1002/cpps.50.
Membrane proteins are the molecular interface of the cell and its environs; however, studies of membrane proteins are highly technically challenging, mainly due to instability of the isolated protein. Towards the production of antibodies that recognize properly folded and stabilized forms of membrane protein antigen, we describe a DNA-based immunization method for mice that expresses the antigen in the membranes of dendritic cells, thus allowing direct presentation to the immune system. This genetic immunization approach employs a highly efficient method of biolistic delivery based on DNA-gold micronanoplexes, which are complexes of micron-sized gold particles that allow dermal penetration and nanometer-sized gold particles that provide a higher surface area for DNA binding than micron gold alone. In contrast to antibodies derived from immunizations with detergent-solubilized protein or with protein fragments, antibodies from genetic immunization are expected to have a high capacity for binding conformational epitopes and for modulating membrane protein activity. © 2018 by John Wiley & Sons, Inc.
膜蛋白是细胞与其周围环境的分子界面;然而,膜蛋白的研究在技术上极具挑战性,主要是因为分离出的蛋白不稳定。为了产生能够识别正确折叠和稳定形式的膜蛋白抗原的抗体,我们描述了一种基于DNA的小鼠免疫方法,该方法在树突状细胞的膜中表达抗原,从而使其能够直接呈递给免疫系统。这种基因免疫方法采用了一种基于DNA-金微米纳米复合物的高效生物弹道递送方法,该复合物是微米级金颗粒的复合物,可实现皮肤穿透,而纳米级金颗粒比单独的微米金提供更高的DNA结合表面积。与用去污剂溶解的蛋白或蛋白片段免疫产生的抗体相比,基因免疫产生的抗体有望具有高结合构象表位和调节膜蛋白活性的能力。© 2018约翰威立国际出版公司