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通过杆状病毒表达-脂质体融合方法制备连接蛋白 43 整合的巨大脂质体。

Preparation of connexin43-integrated giant Liposomes by a baculovirus expression-liposome fusion method.

机构信息

Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan.

出版信息

Biotechnol Bioeng. 2010 Dec 1;107(5):836-43. doi: 10.1002/bit.22845.

Abstract

Connexin-43 (Cx43) containing giant liposomes (GL) were prepared by a baculovirus expression-liposome fusion method. Recombinant budded viruses expressing Cx43 were prepared and then fused with GLs containing DOPG/DOPC at pH 4.5. Connexon formation on the GL membrane was observed by transmission electron microscope. Hydrophilic fluorescent dye transfers were observed through a Cx43-mediated pathway not only between Sf9 (Spodoptera frugiperda) cells with Cx43 but also from giant Cx43 liposomes to Cx43-expressing U2OS cells (human osteosarcoma cell). The functional connexin-containing liposome is expected to be useful for cellular cytosolic delivery systems. The original orientation and function of Cx43 was maintained after integration into the liposomes. The liposome fusion method will create new opportunities as a tool for analysis of channel membrane proteins.

摘要

通过杆状病毒表达-脂质体融合方法制备了含有连接蛋白 43(Cx43)的巨大脂质体(GL)。制备了表达 Cx43 的重组出芽病毒,然后在 pH 4.5 下与含有 DOPG/DOPC 的 GL 融合。通过透射电子显微镜观察 GL 膜上的连接子形成。通过 Cx43 介导的途径观察到亲水性荧光染料转移,不仅在具有 Cx43 的 Sf9(草地贪夜蛾)细胞之间,而且从巨大的 Cx43 脂质体到表达 Cx43 的 U2OS 细胞(人骨肉瘤细胞)之间。功能性连接蛋白脂质体有望成为细胞胞质内递药系统的有用工具。Cx43 在整合到脂质体后,其原始取向和功能得以保持。脂质体融合方法将作为分析通道膜蛋白的工具创造新的机会。

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