Godfrey W, Doe B, Wofsy L
Proc Natl Acad Sci U S A. 1983 Apr;80(8):2267-71. doi: 10.1073/pnas.80.8.2267.
Antibody-directed targeting of vesicles to cells dramatically enhances polyethylene glycol-mediated fusion and microinjection. Sealed erythrocyte ghosts, containing fluorescent bovine serum albumin, were targeted to murine spleen and thymus cells, and to lymphocyte, monocyte, and fibroblast cell lines. In all cases, targeted cell populations showed substantial levels of microinjection, whereas populations treated with the fusogen in the absence of targeting were not significantly microinjected. To achieve attachment of vesicles to selected cells, the cells were first labeled with biotin-modified antibody then treated with sealed ghosts prepared from avidin-coupled erythrocytes. This procedure should prove useful when the injection of specific cell populations is desired, or with cell types such as lymphocytes that are difficult to fuse, or when the use of limited reagents necessitates high injection efficiencies.
通过抗体将囊泡靶向细胞可显著增强聚乙二醇介导的融合和显微注射。含有荧光牛血清白蛋白的密封红细胞血影被靶向到小鼠脾脏和胸腺细胞以及淋巴细胞、单核细胞和成纤维细胞系。在所有情况下,靶向细胞群体都显示出大量的显微注射,而在没有靶向的情况下用融合剂处理的群体则没有明显的显微注射。为了实现囊泡与选定细胞的附着,首先用生物素修饰的抗体标记细胞,然后用从抗生物素蛋白偶联的红细胞制备的密封血影处理。当需要注射特定细胞群体时,或者对于诸如淋巴细胞等难以融合的细胞类型,或者当使用有限的试剂需要高注射效率时,该方法应被证明是有用的。