Dendritic molecular transporters provide control of delivery to intracellular compartments

被引:48
作者
Huang, Kui
Voss, Bryan
Kumar, Disha
Hamm, Heidi E.
Harth, Eva
机构
[1] Vanderbilt Univ, Med Ctr, Dept Pharmacol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Chem, Nashville, TN 37235 USA
关键词
D O I
10.1021/bc060287a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Novel biocompatible macromolecular vectors were developed that not only enable transport of bioactive cargo across the cell membrane but also control the delivery into defined intracellular compartments. This work describes the synthesis and design of two non-peptidic fluorescently labeled Newkome-type dendrimers, differentiated over a varied alkyl spacer with guanidine end moieties. The internalization of the fluorescein-labeled molecular transporter into mammalian cells showed strong subcellular localizations, evident with both live cells and fixed cells costained with DAPI, a nuclear stain. We observed that the subcellular distribution of these vectors varied significantly, as one of the vectors concentrates in the nucleus (FD-1) while the other (FD-2) concentrates in the cytosol. All experiments performed with NIH-3T3 fibroblasts and human microvascular endothelial cells (HMEC) showed similar results. The differential localization patterns of the two molecular transporters can be controlled through the variation of alkyl spacer length at the terminal generation of the dendrimer. Intracellular delivery of bioactive entities into specific subcellular locations, utilizing this practical approach, might overcome limitations in drug delivery and pioneer future technologies in drug transport.
引用
收藏
页码:403 / 409
页数:7
相关论文
共 31 条
[1]   Protein delivery using VP22 [J].
Bennett, RP ;
Dalby, B .
NATURE BIOTECHNOLOGY, 2002, 20 (01) :20-20
[2]   Tat peptide-mediated cellular delivery:: back to basics [J].
Brooks, H ;
Lebleu, B ;
Vivès, E .
ADVANCED DRUG DELIVERY REVIEWS, 2005, 57 (04) :559-577
[3]   Dendritic oligoguanidines as intracellular translocators [J].
Chung, HH ;
Harms, G ;
Seong, CM ;
Choi, BH ;
Min, CH ;
Taulane, JP ;
Goodman, M .
BIOPOLYMERS, 2004, 76 (01) :83-96
[4]   Novel human-derived cell-penetrating peptides for specific subcellular delivery of therapeutic biomolecules [J].
De Coupade, C ;
Fittipaldi, A ;
Chagnas, V ;
Michel, M ;
Carlier, S ;
Tasciott, E ;
Darmon, A ;
Ravel, D ;
Kearsey, J ;
Giacca, M ;
Cailler, F .
BIOCHEMICAL JOURNAL, 2005, 390 :407-418
[5]   Tat peptide as an efficient molecule to translocate gold nanoparticles into the cell nucleus [J].
de la Fuente, JM ;
Berry, CC .
BIOCONJUGATE CHEMISTRY, 2005, 16 (05) :1176-1180
[6]  
DEROSSI D, 1994, J BIOL CHEM, V269, P10444
[7]   Triurethane-protected guanidines and triflyldiurethane-protected guanidines: New reagents for guanidinylation reactions [J].
Feichtinger, K ;
Sings, HL ;
Baker, TJ ;
Matthews, K ;
Goodman, M .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (23) :8432-8439
[8]   Cellular delivery of impermeable effector molecules in the form of conjugates with peptides capable of mediating membrane translocation [J].
Fischer, PM ;
Krausz, E ;
Lane, DP .
BIOCONJUGATE CHEMISTRY, 2001, 12 (06) :825-841
[9]  
FUKATI S, 2006, BIOPOLYMERS, V84, P241
[10]   Arginine-rich peptides - An abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery [J].
Futaki, S ;
Suzuki, T ;
Ohashi, W ;
Yagami, T ;
Tanaka, S ;
Ueda, K ;
Sugiura, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (08) :5836-5840