Interface Engineering Catalytic Graphene for Smart Colorimetric Biosensing
Source abstract
Abstract
Herein a hybrid catalyst consisting of "naked" Au-NPs in situ grown on graphene sheets is engineered, which exhibits a synergetic effect in mimicking peroxidase at its interface, although free Au-NPs or graphene alone has very little activity. What is more, one of the unique features of our synergetic catalyst is that its interface can be reversibly switched from "inactive" to "active" upon treatment with different ssDNA species in solution, thus providing a powerful and versatile basis for designing graphene/DNA-based label-free colorimetric biosensors. Compared with other signal transduction modes in traditional graphene/aptamer-based systems, our novel signaling strategy not only avoids any labeling or modification procedures but also reduces the background signal due to the "off-on" switching mode during the sensing. Furthermore, this facile and general approach can be applicable to the other extended graphene/aptamer-based systems for colorimetric detection of a wide range of analytes. We envision that the tunable graphene-based smart interface could find potential applications in the development of biocatalysis, bioassays, and smart material devices in the future.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced biosensing and bioanalysis techniques · Advanced Nanomaterials in Catalysis · Nanocluster Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Environmental Science and Technology, Key Laboratory of Industrial Ecology and Environmental Engineering (Ministry of Education, China), Dalian University of Technology, Dalian, 116024, China
References (71)
Show source-provided references
1. Novoselov K. S. · Science · 2004 · 306 · 66610.1126/science.1102896 ↗
2. Geim A. K. · Nat. Mater. · 2007 · 6 · 18310.1038/nmat1849 ↗
3. Nair R. R. · Science · 2008 · 320 · 130810.1126/science.1156965 ↗
4. Dikin D. A. · Nature · 2007 · 448 · 45710.1038/nature06016 ↗
5. Zhu Y. W. · Adv. Mater. · 2010 · 22 · 390610.1002/adma.201001068 ↗
6. Pumera M. · Mater. Today · 2011 · 14 · 30810.1016/S1369-7021(11)70160-2 ↗
7. Shan C. · Anal. Chem. · 2009 · 81 · 237810.1021/ac802193c ↗
8. Mohanty N. · Nano Lett. · 2008 · 8 · 446910.1021/nl802412n ↗
9. Ang P. K. · J. Am. Chem. Soc. · 2008 · 130 · 1439210.1021/ja805090z ↗
10. Ren W. · ACS Nano · 2011 · 5 · 642510.1021/nn201606r ↗
11. Jung J. H. · Angew. Chem., Int. Ed. · 2010 · 49 · 570810.1002/anie.201001428 ↗
12. Bai L. · Biomaterials · 2012 · 33 · 109010.1016/j.biomaterials.2011.10.012 ↗
13. Lin L. · Analyst · 2011 · 136 · 473210.1039/c1an15610a ↗
14. Liu F. · Carbon · 2012 · 50 · 12310.1016/j.carbon.2011.07.061 ↗
15. Pruneanu S. · J. Phys. Chem. C · 2011 · 115 · 2338710.1021/jp206945e ↗
16. Ellington A. D. · Nature · 1990 · 346 · 81810.1038/346818a0 ↗
17. Liu J. · Chem. Rev. · 2009 · 109 · 194810.1021/cr030183i ↗
18. Lu C. H. · Angew. Chem., Int. Ed. · 2009 · 48 · 478510.1002/anie.200901479 ↗
19. Chang H. · Anal. Chem. · 2010 · 82 · 234110.1021/ac9025384 ↗
20. He S. · Adv. Funct. Mater. · 2010 · 20 · 45310.1002/adfm.200901639 ↗
21. Wang Y. · J. Am. Chem. Soc. · 2010 · 132 · 927410.1021/ja103169v ↗
22. Dong H. · Anal. Chem. · 2010 · 82 · 551110.1021/ac100852z ↗
23. Liu M. · Chem. Commun. · 2010 · 46 · 790910.1039/c0cc02085k ↗
24. Wang L. · Adv. Mater. · 2011 · 23 · 438610.1002/adma.201102227 ↗
25. Tang D. · Anal. Chem. · 2011 · 83 · 725510.1021/ac201891w ↗
26. Gulbakan B. · J. Am. Chem. Soc. · 2010 · 132 · 1740810.1021/ja109042w ↗
27. Guo S. · Anal. Chem. · 2011 · 83 · 803510.1021/ac2019552 ↗
28. Ohno Y. · J. Am. Chem. Soc. · 2010 · 132 · 1801210.1021/ja108127r ↗
29. Zhang X. · Chem. Commun. · 2011 · 47 · 492910.1039/c1cc10830a ↗
30. Xiang Y. · J. Am. Chem. Soc. · 2009 · 131 · 1535210.1021/ja905854a ↗
31. Wang Y. · Anal. Chem. · 2009 · 81 · 970310.1021/ac901906w ↗
32. Balapanuru J. · Angew. Chem., Int. Ed. · 2010 · 49 · 654910.1002/anie.201001004 ↗
33. Liu M. · Chem. Commun. · 2011 · 47 · 774910.1039/c1cc12006a ↗
34. Cai L. · Anal. Chem. · 2011 · 83 · 784910.1021/ac2016135 ↗
35. Bonanni A. · ACS Nano · 2011 · 5 · 235610.1021/nn200091p ↗
36. Wang L. · Chem. Commun. · 2011 · 47 · 779410.1039/c1cc11373a ↗
37. Wang H. · J. Am. Chem. Soc. · 2010 · 132 · 1397810.1021/ja105296a ↗
38. Zhou Y. · Chem. Mater. · 2009 · 21 · 295010.1021/cm9006603 ↗
39. Yoo E. · Nano Lett. · 2009 · 9 · 225510.1021/nl900397t ↗
40. Chen X. · J. Am. Chem. Soc. · 2011 · 133 · 369310.1021/ja110313d ↗
41. Jasuja K. · ACS Nano · 2009 · 3 · 235810.1021/nn900504v ↗
42. Gao L. Z. · Nat. Nanotechnol. · 2007 · 2 · 57710.1038/nnano.2007.260 ↗
43. Song Y. · Adv. Mater. · 2010 · 22 · 220610.1002/adma.200903783 ↗
44. He W. · Biomaterials · 2011 · 32 · 113910.1016/j.biomaterials.2010.09.040 ↗
45. Wang X. · Nano Res. · 2011 · 4 · 90810.1007/s12274-011-0147-4 ↗
46. Liang Y. · Nat. Mater. · 2011 · 10 · 78010.1038/nmat3087 ↗
47. Guo Y. · ACS Nano · 2011 · 5 · 128210.1021/nn1029586 ↗
48. Johari P. · ACS Nano · 2011 · 5 · 764010.1021/nn202732t ↗
49. Luque G. L. · Electrochim. Acta · 2010 · 56 · 52310.1016/j.electacta.2010.09.016 ↗
50. Ran Q. · Appl. Phys. Lett. · 2009 · 94 · 10351110.1063/1.3095438 ↗
51. Zhou M. · J. Chem. Phys. · 2010 · 132 · 19470410.1063/1.3427246 ↗
52. Zhang Z. · J. Am. Chem. Soc. · 2003 · 125 · 795910.1021/ja034830z ↗
53. Giovannetti G. · Phys. Rev. Lett. · 2008 · 101 · 02680310.1103/PhysRevLett.101.026803 ↗
54. Sundaram R. S. · Nano Lett. · 2011 · 11 · 383310.1021/nl201907u ↗
55. Das A. · Nat. Nanotechnol. · 2008 · 3 · 21010.1038/nnano.2008.67 ↗
56. Lee J. · ACS Nano · 2011 · 5 · 60810.1021/nn103004c ↗
57. Lin Y. C. · Appl. Phys. Lett. · 2010 · 96 · 13311010.1063/1.3368697 ↗
58. Huh S. · ACS Nano · 2011 · 5 · 363910.1021/nn1035203 ↗
59. Pinto H. · Phys. Status Solidi A · 2010 · 207 · 213110.1002/pssa.201000009 ↗
60. Subrahmanyam K. S. · Chem. Phys. Lett. · 2010 · 497 · 7010.1016/j.cplett.2010.07.091 ↗
61. Tang Y. · J. Am. Chem. Soc. · 2009 · 131 · 1320010.1021/ja904595t ↗
62. Lu Y. H. · J. Phys. Chem. C · 2009 · 113 · 2015610.1021/jp908829m ↗
63. Varghese N. · ChemPhysChem · 2009 · 10 · 30610.1002/cphc.200800459 ↗
64. Li H. · J. Am. Chem. Soc. · 2004 · 126 · 1095810.1021/ja048749n ↗
65. Swathi R. S. · J. Chem. Phys. · 2008 · 129 · 05470310.1063/1.2956498 ↗
66. Gaylord B. S. · J. Am. Chem. Soc. · 2003 · 125 · 89610.1021/ja027152+ ↗
67. Syvanen A. C. · Nat. Rev. Genet. · 2001 · 2 · 93010.1038/35103535 ↗
68. Liu S. · Anal. Chem. · 2011 · 83 · 475210.1021/ac200624f ↗
69. Yoshida W. · Biosens. Bioelectron. · 2009 · 24 · 111610.1016/j.bios.2008.06.016 ↗
70. Zhao X. · Anal. Chem. · 2011 · 83 · 506210.1021/ac200843x ↗
71. Tang Y. L. · J. Am. Chem. Soc. · 2006 · 128 · 1497210.1021/ja065159b ↗