线粒体
细胞生物学
线粒体内膜
细胞穿透肽
化学
线粒体膜转运蛋白
生物物理学
线粒体基质
活力测定
细胞
肽
生物化学
生物
胞浆
酶
作者
George Appiah Kubi,Ziqing Qian,Souad Amiar,Ashweta Sahni,Robert V. Stahelin,Dehua Pei
标识
DOI:10.1002/anie.201811940
摘要
Mitochondrial dysfunction is linked to a variety of human illnesses, but selective delivery of therapeutics into the mitochondrion is challenging. Now a family of amphipathic cell-penetrating motifs (CPMs) is presented, consisting of four guanidinium groups and one or two aromatic hydrophobic groups (naphthalene) assembled through a central scaffold (a benzene ring). The CPMs and CPM-cargo conjugates efficiently enter the interior of cultured mammalian cells and are specifically localized into the mitochondrial matrix, as revealed by high-resolution confocal microscopy. With a membrane-impermeable peptide as cargo, the CPMs exhibited ≥170-fold higher delivery efficiency than previous mitochondrial delivery vehicles. Conjugation of a small-molecule inhibitor of heat shock protein 90 to a CPM resulted in accumulation of the inhibitor inside the mitochondrial matrix with greatly enhanced anticancer activity. The CPMs showed minimal effect on the viability or the mitochondrial membrane potential of mammalian cells.
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