journal article·2012-04-24

DNA-Hosted Copper Nanoclusters for Fluorescent Identification of Single Nucleotide Polymorphisms

Xiaofang Jia, Jing Li, Lei Han, Jiangtao Ren, Xuan Yang, Erkang Wang

ACS Nano· Volume 6· Issue 4
Publisher page

Abstract

Metal nanoclusters have received considerable interest due to their unique properties and potential applications in numerous fields. Particularly, newly emerging Cu nanoclusters offer excellent potential as functional biological probes. In this work, we for the first time report that the fluorescence of DNA-hosted Cu nanoclusters is very sensitive to base type located in the major groove. This intriguing finding provides a sensitive fluorimetric diagnostic of the mismatch type in a specific DNA sequence, which is difficult to achieve by traditional methods. Furthermore, the research results have shed some light on the luminescent mechanism of Cu nanoclusters. Owing to its high specificity and easy operation without rigorously controlled temperature and arduous probe DNA design, it is expected that the proposed procedure can provide a tool for early diagnosis and risk assessment of malignancy.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanocluster Synthesis and Applications · Advanced biosensing and bioanalysis techniques · Gold and Silver Nanoparticles Synthesis and Applications

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

Affiliations

State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, Jilin 130022, People's Republic of China, and Graduate School of the Chinese Academy of Sciences, Beijing 100039, People's Republic of China

References (41)

Show source-provided references
1. Jin R. · Chem.–Eur. J. · 2011 · 17 · 658410.1002/chem.201002390 ↗
2. Xu H. X. · Adv. Mater. · 2010 · 22 · 107810.1002/adma.200904199 ↗
3. Tanaka S.-I. · Angew. Chem., Int. Ed. · 2011 · 50 · 43110.1002/anie.201004907 ↗
4. Zhou C. · Angew. Chem., Int. Ed. · 2011 · 50 · 316810.1002/anie.201007321 ↗
5. Wu Z. K. · J. Am. Chem. Soc. · 2009 · 131 · 1667210.1021/ja907627f ↗
6. Rao T. U. B. · Angew. Chem., Int. Ed. · 2010 · 49 · 392510.1002/anie.200907120 ↗
7. Yu M. · J. Am. Chem. Soc. · 2011 · 133 · 1101410.1021/ja201930p ↗
8. Richards C. I. · J. Am. Chem. Soc. · 2008 · 130 · 503810.1021/ja8005644 ↗
9. Yeh H. C. · Nano Lett. · 2010 · 10 · 310610.1021/nl101773c ↗
10. Gwinn E. G. · Adv. Mater. · 2008 · 20 · 27910.1002/adma.200702380 ↗
11. Guo W. W. · Chem. Commun. · 2009 · 339510.1039/b821518a ↗
12. Chen W.-Y. · Anal. Chem. · 2011 · 83 · 945010.1021/ac202162u ↗
13. Yang S. W. · Anal. Chem. · 2011 · 83 · 693510.1021/ac201903n ↗
14. Sharma J. · Chem. Commun. · 2011 · 47 · 229410.1039/C0CC03711G ↗
15. Nakatani K. · ChemBioChem · 2004 · 5 · 162310.1002/cbic.200400161 ↗
16. Lyamichev V. · Nat. Biotechnol. · 1999 · 17 · 29210.1038/7044 ↗
17. Wilhelmsson L. M. · Nucleic Acids Res. · 2002 · 30 · e310.1093/nar/30.2.e3 ↗
18. Wang D. G. · Science · 1998 · 280 · 107710.1126/science.280.5366.1077 ↗
19. Cosnier S. · Analyst · 2008 · 133 · 98410.1039/b803083a ↗
20. Moran N. · Chem. Commun. · 2006 · 500310.1039/b611650g ↗
21. Yamana K. · Chem. Commun. · 2005 · 250910.1039/b502033f ↗
22. Duprey J.-L. H. A. · Chem. Commun. · 2011 · 47 · 662910.1039/c1cc11205h ↗
23. Zeglis B. M. · J. Am. Chem. Soc. · 2006 · 128 · 565410.1021/ja061409c ↗
24. Granzhan A. · Chem.–Eur. J. · 2009 · 15 · 131410.1002/chem.200802421 ↗
25. Guo W. W. · J. Am. Chem. Soc. · 2010 · 132 · 93210.1021/ja907075s ↗
26. Rotaru A. · Angew. Chem., Int. Ed. · 2010 · 49 · 566510.1002/anie.200907256 ↗
27. Rucker V. C. · J. Am. Chem. Soc. · 2003 · 125 · 119510.1021/ja021011q ↗
28. Kim M.-J. · Chem. Phys. Lett. · 2011 · 505 · 5710.1016/j.cplett.2011.02.021 ↗
29. Andrushchenko V. · Biopolymers · 2003 · 72 · 37410.1002/bip.10439 ↗
30. Vilar-Vidal N. · J. Phys. Chem. C · 2010 · 114 · 1592410.1021/jp911380s ↗
31. Lisiecki I. · J. Phys. Chem. · 1996 · 100 · 416010.1021/jp9523837 ↗
32. St-Louis M. · Hum. Mutat. · 1997 · 9 · 29110.1002/(SICI)1098-1004(1997)9:4<291::AID-HUMU1>3.0.CO;2-9 ↗
33. Kypr J. · Nucleic Acids Res. · 2009 · 37 · 171310.1093/nar/gkp026 ↗
34. Yam V. W.-W. · Angew. Chem., Int. Ed. · 2000 · 39 · 168310.1002/(SICI)1521-3773(20000502)39:9<1683::AID-ANIE1683>3.0.CO;2-1 ↗
35. Yam V. W.-W. · Angew. Chem., Int. Ed. · 1999 · 38 · 19710.1002/(SICI)1521-3773(19990115)38:1/2<197::AID-ANIE197>3.0.CO;2-Z ↗
36. Wu Z. · Nano Lett. · 2010 · 10 · 256810.1021/nl101225f ↗
37. Seidel C. A. M. · J. Phys. Chem. · 1996 · 100 · 554110.1021/jp951507c ↗
38. Bahr M. · Nucleic Acids Res. · 2008 · 36 · 500010.1093/nar/gkn392 ↗
39. Qin W. J. · Nucleic Acids Res. · 2007 · 35 · e11110.1093/nar/gkm602 ↗
40. Kanjanawarut R. · Anal. Chem. · 2009 · 81 · 612210.1021/ac900525k ↗
41. Farjami E. · Anal. Chem. · 2011 · 83 · 159410.1021/ac1032929 ↗