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细胞穿透大分子:两亲性磷脂聚合物直接穿透活细胞的质膜。

Cell-penetrating macromolecules: direct penetration of amphipathic phospholipid polymers across plasma membrane of living cells.

机构信息

Department of Materials Engineering, School of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo 113-8656, Japan.

出版信息

Biomaterials. 2010 Mar;31(8):2380-7. doi: 10.1016/j.biomaterials.2009.11.095. Epub 2009 Dec 9.

Abstract

Nanoscaled materials are normally engulfed in endosomes by energy-dependent endocytosis and fail to access the cytosolic cell machinery. Although some biomolecules may penetrate non-endocytically or fuse with plasma membranes without overt membrane disruption, to date no synthetic macromolecule of comparable size has been shown to exhibit this property. Here, we discovered mechanism of direct cell membrane penetration using synthetic phospholipid polymers. These water-soluble amphiphilic phospholipid polymers enter the cytoplasm of living mammalian cells in vitro within a few minutes without overt bilayer disruption even under conditions where energy-dependent endocytic uptakes are blocked. Furthermore, targeted cytosolic distribution to cell organelles was achieved by selecting specific fluorescent tags to the polymers. Thus, the phospholipid polymers can provide a new way of thinking about access to the cellular interior, namely direct membrane penetration.

摘要

纳米级材料通常通过能量依赖的内吞作用被内体吞噬,无法进入细胞质细胞机制。虽然一些生物分子可能通过非内吞作用穿透或与质膜融合而不明显破坏膜,但迄今为止,还没有显示出具有类似大小的合成大分子具有这种特性。在这里,我们发现了使用合成磷脂聚合物进行直接细胞膜穿透的机制。这些水溶性两亲性磷脂聚合物在没有明显双层破坏的情况下,在能量依赖性内吞作用被阻断的情况下,在几分钟内进入体外活哺乳动物细胞的细胞质。此外,通过选择聚合物上的特定荧光标记物,实现了靶向细胞质细胞器的分布。因此,磷脂聚合物可以为进入细胞内部提供一种新的思路,即直接的细胞膜穿透。

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