Rapid Covalent Ligation of Fluorescent Peptides to Water Solubilized Quantum Dots

被引:65
作者
Blanco-Canosa, Juan B. [1 ,2 ]
Medintz, Igor L. [3 ]
Farrell, Dorothy [4 ]
Mattoussi, Hedi [4 ]
Dawson, Philip E. [1 ,2 ]
机构
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[3] USN, Ctr Bio Mol Sci & Engn, Res Lab, Washington, DC 20375 USA
[4] USN, Div Opt Sci, Res Lab, Washington, DC 20375 USA
关键词
RESONANCE ENERGY-TRANSFER; IN-VIVO; NUCLEOPHILIC CATALYSIS; LIVING CELLS; PROTEIN; NANOCRYSTALS; LIGANDS; COMPLEXES; MOLECULES; CHEMISTRY;
D O I
10.1021/ja910988d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Water solubilized nanoparticles such as CdSe-ZnS core-shell nanocrystals (quantum dots, QDs) have great potential in bioimaging and sensing applications due to their excellent photophysical properties. However, the efficient modification of QDs with complex biomolecules represents a significant challenge. Here, we describe a straightforward arylhydrazone approach for the chemoselective covalent modification of QDs that is compatible with neutral pH and micromolar concentrations of the peptide target. The kinetics of covalent modification can be monitored spectroscopically at 354 nm in the presence of the QD and average peptide/QD ratios from 2:1 to 11:1 were achieved with excellent control over the desired valency. These results suggest that aniline catalyzed hydrazone ligation has the potencial to provide a general method for the controlled assembly of a variety of nanoparticle-biomolecule hybrids.
引用
收藏
页码:10027 / 10033
页数:7
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