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Discovery of functional monoclonal antibodies targeting G-protein-coupled receptors and ion channels.靶向G蛋白偶联受体和离子通道的功能性单克隆抗体的发现。
Biochem Soc Trans. 2016 Jun 15;44(3):831-7. doi: 10.1042/BST20160028.
2
DNA immunization as a technology platform for monoclonal antibody induction.DNA免疫作为诱导单克隆抗体的技术平台。
Emerg Microbes Infect. 2016 Apr 6;5(4):e33. doi: 10.1038/emi.2016.27.
3
Cryo-EM structure of a native, fully glycosylated, cleaved HIV-1 envelope trimer.天然、完全糖基化、裂解的HIV-1包膜三聚体的冷冻电镜结构
Science. 2016 Mar 4;351(6277):1043-8. doi: 10.1126/science.aad2450.
4
Polyclonal Antibody Production for Membrane Proteins via Genetic Immunization.通过基因免疫制备膜蛋白的多克隆抗体
Sci Rep. 2016 Feb 24;6:21925. doi: 10.1038/srep21925.
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Innate Immune Signaling by, and Genetic Adjuvants for DNA Vaccination.DNA疫苗接种的固有免疫信号传导及遗传佐剂
Vaccines (Basel). 2013 Jul 18;1(3):278-92. doi: 10.3390/vaccines1030278.
6
Generation of recombinant antibody fragments for membrane protein crystallization.用于膜蛋白结晶的重组抗体片段的产生。
Methods Enzymol. 2015;557:201-18. doi: 10.1016/bs.mie.2014.12.029. Epub 2015 Mar 24.
7
Discovery of functional antibodies targeting ion channels.靶向离子通道的功能性抗体的发现。
J Biomol Screen. 2015 Apr;20(4):454-67. doi: 10.1177/1087057114560698. Epub 2014 Dec 3.
8
Improving DNA vaccine performance through vector design.通过载体设计提高DNA疫苗性能。
Curr Gene Ther. 2014;14(3):170-89. doi: 10.2174/156652321403140819122538.
9
Generation of antibodies against membrane proteins.针对膜蛋白的抗体生成。
Biochim Biophys Acta. 2014 Nov;1844(11):1920-1924. doi: 10.1016/j.bbapap.2014.08.007. Epub 2014 Aug 15.
10
Mouse monoclonal antibodies to transient receptor potential ankyrin 1 act as antagonists of multiple modes of channel activation.鼠单克隆抗体瞬时受体电位锚蛋白 1 作为拮抗剂的多种模式的通道激活。
J Pharmacol Exp Ther. 2014 Aug;350(2):223-31. doi: 10.1124/jpet.114.215574. Epub 2014 Jun 3.

利用DNA-金微米纳米复合物通过基因枪免疫法生成针对膜蛋白的高特异性抗体

Generation of High-Specificity Antibodies against Membrane Proteins Using DNA-Gold Micronanoplexes for Gene Gun Immunization.

作者信息

Hansen Debra T, Craciunescu Felicia M, Fromme Petra, Johnston Stephen A, Sykes Kathryn F

机构信息

Biodesign Center for Applied Structural Discovery, Arizona State University, Tempe, Arizona.

Biodesign Center for Innovations in Medicine, Arizona State University, Tempe, Arizona.

出版信息

Curr Protoc Protein Sci. 2018 Feb 21;91:29.20.1-29.20.22. doi: 10.1002/cpps.50.

DOI:10.1002/cpps.50
PMID:29516482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5846111/
Abstract

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.

摘要

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