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用于溶酶体靶向的末端功能化6-磷酸甘露糖糖多肽的可控合成。

Controlled Synthesis of End-Functionalized Mannose-6-phosphate Glycopolypeptides for Lysosome Targeting.

作者信息

Das Soumen, Parekh Nimisha, Mondal Basudeb, Gupta Sayam Sen

机构信息

CReST Chemical Engineering Division, CSIR National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008, India.

出版信息

ACS Macro Lett. 2016 Jul 19;5(7):809-813. doi: 10.1021/acsmacrolett.6b00297. Epub 2016 Jun 22.

Abstract

The ubiquitous expression of the mannose-6-phosphate receptor on the majority of human cells makes it a valid target in the quest to deliver therapeutics selectively to the lysosome. In this work end-functionalized polyvalent mannose-6-phosphate glycopolypeptides (M6P-GPs) with high molecular weights (up to 22 kDa) have been synthesized via NCA polymerization. These synthetic M6P-GPs were found to display minimal toxicity to cells in vitro and show exceptional selectivity for trafficking into lysosomes in various cell lines. Comparison of the cellular uptake behavior of M6P-GP and the corresponding mannose-GP polymer reveals that incorporation of the phosphate moiety at the 6-position of mannose completely alters its trafficking behavior and becomes exclusively lysosome specific. We also demonstrate that trafficking of M6P-GPs in mammalian cells is likely associated with the CI-MPR receptor pathway.

摘要

甘露糖-6-磷酸受体在大多数人类细胞中普遍表达,这使其成为将治疗药物选择性递送至溶酶体研究中的一个有效靶点。在这项工作中,通过NCA聚合反应合成了具有高分子量(高达22 kDa)的末端功能化多价甘露糖-6-磷酸糖多肽(M6P-GPs)。发现这些合成的M6P-GPs在体外对细胞显示出最小的毒性,并在各种细胞系中表现出对溶酶体转运的卓越选择性。M6P-GP与相应的甘露糖-GP聚合物的细胞摄取行为比较表明,在甘露糖的6位引入磷酸部分完全改变了其转运行为,并使其仅对溶酶体具有特异性。我们还证明,M6P-GPs在哺乳动物细胞中的转运可能与CI-MPR受体途径有关。

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