Peptoid transporters: effects of cationic, amphipathic structure on their cellular uptake
Peptoid transporters: effects of cationic, amphipathic structure on their cellular uptake
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DOI：
10.1039/c2mb25197c
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发表时间：
2012-01-01
影响因子：
--
通讯作者：
Barron, Annelise E.
中科院分区：
文献类型：
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作者：
Huang, Wei;Seo, Jiwon;Barron, Annelise E.
两个阳离子，两亲性类肽（聚-N-取代的甘氨酸）被开发为新的分子转运蛋白，具有广泛的细胞摄取，并利用不同的内化机制，从纯阳离子聚胍比较。
Two cationic, amphipathic peptoids (poly-N-substituted glycines) were developed as new molecular transporters, which have extensive cellullar uptake and utilize different internalization mechanisms from purely cationic polyguanidine comparators.