journal article·2015-04-01

Integrated Logic Gate for Fluorescence Turn-on Detection of Histidine and Cysteine Based on Ag/Au Bimetallic Nanoclusters–Cu2+ Ensemble

Jian Sun, Fan Yang, Dan Zhao, Chuanxia Chen, Xiurong Yang

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Abstract

By means of employing 11-mercaptoundecanoic acid (11-MUA) as a reducing agent and protecting ligand, we present straightforward one-pot preparation of fluorescent Ag/Au bimetallic nanoclusters (namely AgAuNCs@11-MUA) from AgNO3 and HAuCl4 in alkaline aqueous solution at room temperature. It is found that the fluorescence of AgAuNCs@11-MUA has been selectively quenched by Cu(2+) ions, and the nonfluorescence off-state of the as-prepared AgAuNCs@11-MUA-Cu(2+) ensemble can be effectively switched on upon the addition of histidine and cysteine. By incorporating Ni(2+) ions and N-ethylmaleimide, this phenomenon is further exploited as an integrated logic gate and a specific fluorescence turn-on assay for selectively and sensitively sensing histidine and cysteine has been designed and established based on the original noncovalent AgAuNCs@11-MUA-Cu(2+) ensemble. Under the optimal conditions, histidine and cysteine can be detected in the concentration ranges of 0.25-9 and 0.25-7 μM; besides, the detection limits are found to be 87 and 111 nM (S/N = 3), respectively. Furthermore, we demonstrate that the proposed AgAuNCs@11-MUA-based fluorescent assay can be successfully utilized for biological fluids sample analysis.
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Research context

OpenAlex topics: Nanocluster Synthesis and Applications · Advanced Nanomaterials in Catalysis · Advanced biosensing and bioanalysis techniques

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, China

University of Chinese Academy of Sciences, Beijing 100039, China

Funding

National Natural Science Foundation of China · Jilin Province

References (42)

Show source-provided references
1. Zhou Y. · Chem. Soc. Rev. · 2012 · 41 · 5210.1039/C1CS15159B ↗
2. Luo Z. T. · Chem. Commun. · 2014 · 50 · 514310.1039/C3CC47512C ↗
3. Xu J. J. · Chem. Soc. Rev. · 2014 · 43 · 160110.1039/C3CS60277J ↗
4. Peng F. · Acc. Chem. Res. · 2014 · 47 · 61210.1021/ar400221g ↗
5. Huang R. C. · ACS Appl. Mater. Interfaces · 2014 · 6 · 2178010.1021/am500534g ↗
6. Yuan X. · Chem.—Asian J. · 2013 · 8 · 85810.1002/asia.201201236 ↗
7. Shang L. · Nano Today · 2011 · 6 · 40110.1016/j.nantod.2011.06.004 ↗
8. Sun J. · J. Mater. Chem. C · 2014 · 2 · 800010.1039/C4TC01489H ↗
9. Guo W. W. · J. Am. Chem. Soc. · 2010 · 132 · 93210.1021/ja907075s ↗
10. Zhang L. B. · Nano Today · 2014 · 9 · 13210.1016/j.nantod.2014.02.010 ↗
11. Yuan Z. Q. · Chem. Commun. · 2014 · 50 · 980010.1039/C4CC02981J ↗
12. Chen W. Y. · Anal. Chem. · 2011 · 83 · 945010.1021/ac202162u ↗
13. Dou X. Y. · Nanoscale · 2014 · 6 · 15710.1039/C3NR04490D ↗
14. Wang S. X. · Angew. Chem., Int. Ed. · 2014 · 53 · 237610.1002/anie.201307480 ↗
15. Zheng J. · Nanoscale · 2012 · 4 · 407310.1039/c2nr31192e ↗
16. Shang L. · Angew. Chem., Int. Ed. · 2013 · 52 · 1115410.1002/anie.201306366 ↗
17. Sun J. · J. Mater. Chem. C · 2013 · 1 · 90810.1039/C2TC00207H ↗
18. Sun J. · J. Mater. Chem. C · 2013 · 1 · 13810.1039/C2TC00021K ↗
19. Huang C. C. · Angew. Chem., Int. Ed. · 2007 · 46 · 682410.1002/anie.200700803 ↗
20. Shang L. · Nanoscale · 2012 · 4 · 415510.1039/c2nr30219e ↗
21. Roy S. · ACS Appl. Mater. Interfaces · 2014 · 6 · 405010.1021/am4055645 ↗
22. Fu Y. · Chem. Commun. · 2005 · 318910.1039/b503772g ↗
23. Reddy G. U. · Chem. Commun. · 2014 · 50 · 989910.1039/C4CC04214J ↗
24. Sun J. · Anal. Chem. · 2014 · 86 · 788310.1021/ac501814u ↗
25. Chen Y. · J. Mater. Chem. C · 2014 · 2 · 408010.1039/c4tc00173g ↗
26. Li P. H. · Anal. Chem. · 2012 · 84 · 548410.1021/ac300332t ↗
27. Kusakari Y. · Curr. Eye Res. · 1997 · 16 · 60010.1076/ceyr.16.6.600.5084 ↗
28. Watanabe M. · Am. J. Clin. Nutr. · 2008 · 87 · 186010.1093/ajcn/87.6.1860 ↗
29. Gazit V. · Amino Acids · 2004 · 26 · 16310.1007/s00726-003-0045-5 ↗
30. Seshadri S. · N. Engl. J. Med. · 2002 · 346 · 47610.1056/NEJMoa011613 ↗
31. Refsum H. · Annu. Rev. Med. · 1998 · 49 · 3110.1146/annurev.med.49.1.31 ↗
32. Chen G. N. · Talanta · 1999 · 49 · 31910.1016/S0039-9140(98)00379-8 ↗
33. You Q. H. · Chem. Commun. · 2014 · 50 · 620710.1039/C4CC00521J ↗
34. Wu P. · Biosens. Bioelectron. · 2010 · 26 · 48510.1016/j.bios.2010.07.068 ↗
35. Wei M. J. · Chem. Commun. · 2013 · 49 · 464010.1039/c3cc39045d ↗
36. Huo Z. Y. · Nano Lett. · 2008 · 8 · 204110.1021/nl8013549 ↗
37. Sun J. · Nanoscale · 2014 · 6 · 544910.1039/c4nr00445k ↗
38. Wang B. · Org. Biomol. Chem. · 2011 · 9 · 403210.1039/c1ob05372h ↗
39. Liu S. Y. · Analyst · 2013 · 138 · 581910.1039/c3an00758h ↗
40. Szacilowski K. · Chem. Rev. · 2008 · 108 · 348110.1021/cr068403q ↗
41. Pu F. · Adv. Mater. · 2014 · 26 · 111110.1002/adma.201304109 ↗
42. Kovach P. M. · Anal. Chem. · 1982 · 54 · 21710.1021/ac00239a016 ↗