Dendritic oligoguanidines as intracellular translocators

被引:49
作者
Chung, HH
Harms, G
Seong, CM
Choi, BH
Min, CH
Taulane, JP
Goodman, M [1 ]
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] LG Biomed Inst, La Jolla, CA 92037 USA
关键词
polyguanidylated dendritic structures; molecular translocators; nonpeptide units; oligoguanidines; fluorescein; green fluorescent protein mutant;
D O I
10.1002/bip.10597
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of polyguanidylated dendritic structures that can be used as molecular translocators have been designed and synthesized based on nonpeptide units. The dendritic oligoguanidines conjugated with fluorescein or with a green fluorescent protein (GFP) mutant as cargos were isolated and characterized. Quantification and time-course analyses of the cellular uptake of the conjugates using HeLa S3 and human cervical carcinoma cells reveal that the polyguanidylated dendrimers have comparable translocation efficiency to the Tat((49-57)) peptide. Furthermore, the deconvolution microscopy image analysis shows that they are located inside the cells. These results clearly show that nonlinear, branched dendritic oligoguanidines are capable of translocation through the cell membrane. This work also demonstrates the potential of these nonpeptidic dendritic oligoguanidines as carriers for intracellular delivery of small molecule drugs, bioactive peptides, and proteins. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:83 / 96
页数:14
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