Hydrazone Ligation Strategy to Assemble Multifunctional Viral Nanoparticles for Cell Imaging and Tumor Targeting

被引:121
作者
Brunel, Florence M. [1 ,2 ]
Lewis, John D. [1 ]
Destito, Giuseppe [1 ,3 ,4 ]
Steinmetz, Nicole F. [1 ,3 ]
Manchester, Marianne [1 ,3 ]
Stuhlmann, Heidi [1 ]
Dawson, Philip E. [1 ,2 ]
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Ctr Integrat Mol Biosci, La Jolla, CA 92037 USA
[4] Univ Magna Graecia di Catanzaro, Dipartimento Med Sperimentale & Clin, I-88100 Catanzaro, Italy
关键词
Viral nanoparticle; chemical ligation; cell imaging; tumor targeting; VEGFR-1; COWPEA MOSAIC-VIRUS; EXPRESSION; PROTEIN; GROWTH; DELIVERY; SURFACE; VEGF;
D O I
10.1021/nl1002526
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multivalent nanoparticle platforms are attractive for biomedical applications because of their improved target specificity, sensitivity, and solubility. However, their controlled assembly remains a considerable challenge, An efficient hydrazone ligation chemistry was applied to the assembly of Cowpea mosaic virus (CPMV) nanoparticles with individually tunable levels of a VEGFR-I ligand and a fluorescent PEGylated peptide. The nanoparticles recognized VEGFR-I on endothelial cell lines and VEGFR I-expressing tumor xenografts in mice, validating targeted CPMV as a nanoparticle platform in vivo.
引用
收藏
页码:1093 / 1097
页数:5
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