Institute of Immunology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
UNIROUEN, INSERM, U1234, Pathophysiology, Autoimmunity, Neuromuscular Diseases and Regenerative THERapies (PANTHER), Normandie University, Rouen, France.
Methods Mol Biol. 2022;2510:129-144. doi: 10.1007/978-1-0716-2384-8_7.
Adeno-associated viruses (AAV) are useful vectors for transducing cells in vitro and in vivo. Targeting of specific cell subsets with AAV is limited by the broad tropism of AAV serotypes. Nanobodies are single immunoglobulin variable domains from heavy chain antibodies that naturally occur in camelids. Their small size and high solubility allow easy reformatting into fusion proteins. In this chapter we provide protocols for inserting a P2X7-specific nanobody into a surface loop of the VP1 capsid protein of AAV2. Such nanobody-displaying recombinant AAV allow 50- to 500-fold stronger transduction of P2X7-expressing cells than the parental AAV. We provide protocols for monitoring the transduction of P2X7-expressing cells by nanobody-displaying rAAV by flow cytometry and fluorescence microscopy.
腺相关病毒(AAV)是体外和体内转导细胞的有用载体。AAV 血清型的广泛嗜性限制了对特定细胞亚群的靶向。纳米抗体是重链抗体的单免疫球蛋白可变结构域,天然存在于骆驼科动物中。它们的体积小、溶解度高,允许轻松地重新构建为融合蛋白。在本章中,我们提供了将 P2X7 特异性纳米抗体插入 AAV2 VP1 衣壳蛋白表面环的方案。这种展示纳米抗体的重组 AAV 允许表达 P2X7 的细胞的转导增强 50-500 倍,而亲本 AAV 则没有。我们提供了通过流式细胞术和荧光显微镜监测表达 P2X7 的细胞被纳米抗体展示 rAAV 转导的方案。