胞浆
细胞内
细菌外膜
小泡
细胞生物学
膜蛋白
细胞膜
细胞
转染
生物
生物物理学
膜
大肠杆菌
化学
生物化学
基因
酶
作者
Huan Wang,Zhiqing Tao,Xiaoling Zhao,Guan Wang,Yun Peng,Yi‐Hao Chen,Juan Zhang,Xu Zhang,Maili Liu,Guosheng Jiang,Lichun He
标识
DOI:10.1021/acsami.3c00427
摘要
Advanced intracellular delivery of proteins has profound applications in both scientific investigations and therapies. However, existing strategies relying on various chemical and physical methods have drawbacks such as the requirement of high concentrations of in vitro prepared target proteins and difficulty in labeling target proteins. Developing new delivery systems integrating the enveloping and labeling of target proteins would bring great advantages for efficient protein transfections. Here, we enriched a high concentration (62 mg/mL) of several target proteins into the outer membrane vesicles (OMVs) of Escherichia coli to employ the native property of OMVs to deliver proteins into the cytosol of eukaryotic cells. The results revealed a high protein transfection efficiency from 90 to 97% for different cell lines. Moreover, the free penetration of molecules less than 600 Da across the membrane of OMVs allows direct labeling of target proteins within OMVs, facilitating the visualization of target proteins. Importantly, the nanobody delivered intracellularly by OMVs retains the biological activity of binding with its target, highlighting the advantages of OMVs as an emerging tool for efficient intracellular delivery of proteins.
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