journal article·2016-12-28

Multifunctional Polymer Ligand Interface CdZnSeS/ZnS Quantum Dot/Cy3-Labeled Protein Pairs as Sensitive FRET Sensors

Hong Yu Yang, Yan Fu, Moon-Sun Jang, Yi Li, Jung Hee Lee, Heeyeop Chae, Doo Sung Lee

Publisher page

Abstract

High-quality CdZnSeS/ZnS alloyed core/thick-shell quantum dots (QDs) as energy donors were first exploited in Förster resonance energy transfer (FRET) applications. A highly efficient ligand-exchange method was used to prepare low toxicity, high quantum yield, stabile, and biocompatible CdZnSeS/ZnS QDs densely capped with multifunctional polymer ligands containing dihydrolipoic acid (DHLA). The resulting QDs can be applied to construct QDs-based Förster resonance energy transfer (FRET) systems by their high affinity interaction with dye cyanine 3 (Cy3)-labeled human serum albumin (HSA). This QD-based FRET protein complex can serve as a sensitive sensor for probing the interaction of clofazimine with proteins using fluorescence spectroscopic techniques. The ability of FRET imaging both in vitro and in vivo not only reveals that the current FRET system can remain intact for 2 h but also confirms the potential of the FRET system to act as a nanocarrier for intracellular protein delivery or to serve as an imaging probe for cancer diagnosis.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Advanced biosensing and bioanalysis techniques · Nanocluster Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine and Center for Molecular and Cellular Imaging, Samsung Biomedical Research Institute, Seoul 135-710, Republic of Korea

Funding

National Research Foundation of Korea

References (45)

Show source-provided references
1. 10.1039/c0cs00224k10.1039/c0cs00224k ↗
2. 10.1021/am404994210.1021/am4049942 ↗
3. 10.1021/ac403846s10.1021/ac403846s ↗
4. 10.1039/C6NR02815B10.1039/C6NR02815B ↗
5. 10.1016/j.bios.2015.06.07610.1016/j.bios.2015.06.076 ↗
6. 10.1039/C5TB00885A10.1039/C5TB00885A ↗
7. 10.1016/j.addr.2015.08.00410.1016/j.addr.2015.08.004 ↗
8. 10.1039/C5NR08284F10.1039/C5NR08284F ↗
9. 10.1021/am302866210.1021/am3028662 ↗
10. 10.1021/ac300049510.1021/ac3000495 ↗
11. 10.1021/bc800089r10.1021/bc800089r ↗
12. 10.1039/c001553a10.1039/c001553a ↗
13. 10.1021/am303072810.1021/am3030728 ↗
14. 10.1021/ja306621n10.1021/ja306621n ↗
15. 10.1002/smll.20140120910.1002/smll.201401209 ↗
16. 10.1021/jp512678j10.1021/jp512678j ↗
17. 10.1021/nn203807710.1021/nn2038077 ↗
18. 10.1039/C6NR01912A10.1039/C6NR01912A ↗
19. 10.1021/am502135h10.1021/am502135h ↗
20. 10.1021/acs.nanolett.5b0344210.1021/acs.nanolett.5b03442 ↗
21. 10.1038/ncomms703610.1038/ncomms7036 ↗
22. 10.1038/nmeth94510.1038/nmeth945 ↗
23. 10.1021/ja809721j10.1021/ja809721j ↗
24. 10.1002/anie.20160059310.1002/anie.201600593 ↗
25. 10.1021/nn204860810.1021/nn2048608 ↗
26. 10.1021/am300098410.1021/am3000984 ↗
27. 10.1002/smll.20120257010.1002/smll.201202570 ↗
28. 10.1021/acsami.5b1016010.1021/acsami.5b10160 ↗
29. 10.1021/jp311238n10.1021/jp311238n ↗
30. 10.1016/j.jphotochem.2007.04.01010.1016/j.jphotochem.2007.04.010 ↗
31. 10.1016/j.bbapap.2008.03.01810.1016/j.bbapap.2008.03.018 ↗
32. 10.1073/pnas.141695111210.1073/pnas.1416951112 ↗
33. 10.1016/j.bcp.2013.12.00710.1016/j.bcp.2013.12.007 ↗
34. 10.1039/C5NR06542A10.1039/C5NR06542A ↗
35. 10.1021/nn500852g10.1021/nn500852g ↗
36. 10.1038/nprot.2015.05010.1038/nprot.2015.050 ↗
37. 10.1039/B813919A10.1039/B813919A ↗
38. 10.1021/ja037088b10.1021/ja037088b ↗
39. 10.1039/C5PY01808K10.1039/C5PY01808K ↗
40. 10.1021/jacs.5b0067110.1021/jacs.5b00671 ↗
41. 10.1039/b815958k10.1039/b815958k ↗
42. 10.1039/c3nr02897f10.1039/c3nr02897f ↗
43. 10.1016/j.addr.2011.09.01110.1016/j.addr.2011.09.011 ↗
44. 10.1016/j.jconrel.2010.03.01910.1016/j.jconrel.2010.03.019 ↗
45. 10.1016/j.drudis.2006.07.00510.1016/j.drudis.2006.07.005 ↗