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阳离子两亲性多聚脯氨酸螺旋 P11LRR 靶向细胞内线粒体。

Cationic amphiphilic polyproline helix P11LRR targets intracellular mitochondria.

机构信息

Department of Chemistry, Purdue University, West Lafayette, IN 47907, United States.

出版信息

J Control Release. 2010 Mar 3;142(2):259-66. doi: 10.1016/j.jconrel.2009.10.012. Epub 2009 Oct 24.

Abstract

We demonstrate that P11LRR, a recently developed amphiphilic polyproline, cell penetrating agent, is able to locate inside the mitochondria of various cell lines when administrated at high concentrations. Mitochondrial targeting was verified by confocal fluorescence co-localization of P11LRR-fluorescein with Mitotracker Red. Elimination of mitochondrial membrane potential dramatically inhibits the localization of P11LRR to mitochondria. Concentration-dependency experiments suggest that cellular internalization of P11LRR occurs via two different pathways: endocytosis and direct transport. Results indicate that the latter pathway predominates at high concentrations of P11LRR, resulting in localization of the agent to the mitochondria. The membrane translocation pathway was further confirmed by two endocytosis inhibitors, cytochalasin D and phenylarsine oxide, and by modulation of plasma membrane potential. The potential of using P11LRR as a mitochondrial drug delivery vector was demonstrated through the delivery of a covalently linked small antioxidant, dimethyltyrosine (Dmt), which allowed for the reduction of chemically induced reactive oxygen species within the mitochondria.

摘要

我们证明,最近开发的一种两亲性多聚脯氨酸、细胞穿透肽 P11LRR,在高浓度给药时能够定位于各种细胞系的线粒体内部。线粒体靶向通过 P11LRR-荧光素与 Mitotracker Red 的共焦荧光共定位来验证。线粒体膜电位的消除显著抑制 P11LRR 定位于线粒体。浓度依赖性实验表明,P11LRR 的细胞内摄取通过两种不同的途径发生:内吞作用和直接转运。结果表明,在后一种途径中,P11LRR 的浓度较高,导致该试剂定位于线粒体。通过两种内吞作用抑制剂细胞松弛素 D 和苯砷氧化物以及对质膜电位的调节进一步证实了膜转位途径。通过递送共价连接的小分子抗氧化剂二甲基酪氨酸(Dmt),证明了 P11LRR 作为线粒体药物递送载体的潜力,这使得能够减少化学诱导的线粒体中活性氧物质的产生。

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