Abstract
The multivalent nature of commercial quantum dots (QDs) and the difficulties associated with producing monovalent dots have limited their applications in biology, where clustering and the spatial organization of biomolecules is often the object of study. We describe here a protocol to produce monovalent quantum dots (mQDs) that can be accomplished in most biological research laboratories via a simple mixing of CdSe/ZnS core/shell QDs with phosphorothioate DNA (ptDNA) of defined length. After a single ptDNA strand has wrapped the QD, additional strands are excluded from the surface. Production of mQDs in this manner can be accomplished at small and large scale, with commercial reagents, and in minimal steps. These mQDs can be specifically directed to biological targets by hybridization to a complementary single stranded targeting DNA. We demonstrate the use of these mQDs as imaging probes by labeling SNAP-tagged Notch receptors on live mammalian cells, targeted by mQDs bearing a benzylguanine moiety.
Original language | English |
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Article number | e52198 |
Journal | Journal of Visualized Experiments |
Issue number | 92 |
DOIs | |
State | Published - 23 Oct 2014 |
Bibliographical note
Publisher Copyright:© JoVE 2006-2014. All Rights Reserved.
Keywords
- Bioengineering
- DNA
- Issue 92
- Monovalent quantum dots
- Nanoparticle bioconjugation
- Phosphorothioate
- SNAP tag
- Single molecule imaging
- Single particle tracking
- Steric exclusion