journal article·2018-03

Multifunctional Poly‐N‐Isopropylacrylamide/DNAzyme Microgels as Highly Efficient and Recyclable Catalysts for Biosensing

Fengyun Li, Chunyan Wang, Weiwei Guo

Advanced Functional Materials· Volume 28· Issue 10
Publisher page

Abstract

Abstract The development of highly efficient, recyclable, and multifunctional biocatalysts is of great importance for various applications, especially in biosensing. In this study, highly catalytic and recyclable DNAzyme functionalized poly‐N‐isopropylacrylamide (pNIPAM) microgels are prepared via one‐step precipitation polymerization. The pNIPAM/DNAzyme microgels exhibit highly catalytic activities in aqueous solution at room temperature, and become hydrophobic and separable from the reaction mixture at temperature higher than the lower critical solution temperature of pNIPAM, which facilitate the recyclable utilization of these catalysts. Different kinds of DNAzyme functionalized catalytic microgels can be facilely prepared via the one‐step synthesis procedure. Two typical catalytic DNA structures, the Mg2+‐dependent DNAzyme and the hemin‐G‐quadruplex horseradish peroxidase (HRP)‐mimicking DNAzyme, are chosen as model systems to validate the feasibility. These pNIPAM/DNAzyme microgel catalysts maintain 80% to 91% initial catalytic activity after eight times of catalysis recycling. Furthermore, the pNIPAM microgels by themselves provide additional interfaces to capturing an enzyme, glucose oxidase, which can cascade with the linked HRP mimicking DNAzymes, to form recyclable bi‐enzyme cascading system for the sensing of glucose.
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Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · Electrochemical sensors and biosensors · Molecular Sensors and Ion Detection

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

Affiliations

College of Chemistry Research Center for Analytical Sciences State Key Laboratory of Medicinal Chemical Biology and Tianjin Key Laboratory of Molecular Recognition and Biosensing Collaborative Innovation Center of Chemical Science and Engineering (Tianjin) Nankai University 94 Weijin Road Tianjin 300071 P. R. China

Funding

National Natural Science Foundation of China

References (72)

Show source-provided references
1. 10.1016/j.tibs.2016.04.01010.1016/j.tibs.2016.04.010 ↗
2. 10.1038/344467a010.1038/344467a0 ↗
3. 10.1016/j.chembiol.2009.01.00810.1016/j.chembiol.2009.01.008 ↗
4. 10.1038/nature1398210.1038/nature13982 ↗
5. 10.1073/pnas.142036111210.1073/pnas.1420361112 ↗
6. 10.1038/nature1647110.1038/nature16471 ↗
7. 10.1002/anie.20090634510.1002/anie.200906345 ↗
8. 10.1021/ja309638j10.1021/ja309638j ↗
9. 10.1016/1074-5521(95)90028-410.1016/1074-5521(95)90028-4 ↗
10. 10.1073/pnas.94.9.426210.1073/pnas.94.9.4262 ↗
11. 10.1021/ja403585e10.1021/ja403585e ↗
12. 10.1021/cr400476k10.1021/cr400476k ↗
13. 10.1093/nar/gkv51910.1093/nar/gkv519 ↗
14. 10.1039/b811349c10.1039/b811349c ↗
15. 10.1038/3795010.1038/37950 ↗
16. 10.1038/3637510.1038/36375 ↗
17. 10.1073/pnas.050373310210.1073/pnas.0503733102 ↗
18. 10.1002/ange.20090037110.1002/ange.200900371 ↗
19. 10.1002/anie.20140462210.1002/anie.201404622 ↗
20. 10.1021/jacs.5b0945710.1021/jacs.5b09457 ↗
21. 10.1039/b718428j10.1039/b718428j ↗
22. 10.1021/acs.analchem.5b0417010.1021/acs.analchem.5b04170 ↗
23. 10.1002/anie.20170005410.1002/anie.201700054 ↗
24. 10.1002/ange.20170005410.1002/ange.201700054 ↗
25. 10.1021/acs.chemrev.7b0006310.1021/acs.chemrev.7b00063 ↗
26. 10.1038/nnano.2010.8810.1038/nnano.2010.88 ↗
27. 10.1002/anie.20050029810.1002/anie.200500298 ↗
28. 10.1002/adsc.20140081810.1002/adsc.201400818 ↗
29. 10.1021/acs.analchem.6b0419010.1021/acs.analchem.6b04190 ↗
30. 10.1038/382607a010.1038/382607a0 ↗
31. 10.1021/ja209351u10.1021/ja209351u ↗
32. 10.1039/c2cc31327h10.1039/c2cc31327h ↗
33. 10.1002/adma.20070150610.1002/adma.200701506 ↗
34. 10.1021/nl071108g10.1021/nl071108g ↗
35. 10.1002/adfm.20040042710.1002/adfm.200400427 ↗
36. 10.1021/acsami.6b1232710.1021/acsami.6b12327 ↗
37. 10.1021/ja991662v10.1021/ja991662v ↗
38. 10.1038/nmat150810.1038/nmat1508 ↗
39. 10.1021/nl049628o10.1021/nl049628o ↗
40. 10.1039/b709817k10.1039/b709817k ↗
41. 10.1002/anie.20060306410.1002/anie.200603064 ↗
42. 10.1002/chem.20090154610.1002/chem.200901546 ↗
43. 10.1021/cm049453j10.1021/cm049453j ↗
44. 10.1002/adma.20070318110.1002/adma.200703181 ↗
45. 10.1002/smll.20090169110.1002/smll.200901691 ↗
46. 10.1021/nn402214e10.1021/nn402214e ↗
47. 10.1016/j.mattod.2016.05.01510.1016/j.mattod.2016.05.015 ↗
48. 10.1038/nnano.2013.25710.1038/nnano.2013.257 ↗
49. 10.1038/ncomms1437810.1038/ncomms14378 ↗
50. 10.1016/0079-6700(92)90023-R10.1016/0079-6700(92)90023-R ↗
51. 10.1039/C2CS35191A10.1039/C2CS35191A ↗
52. 10.1016/S0001-8686(99)00023-810.1016/S0001-8686(99)00023-8 ↗
53. 10.1039/C7SM01558E10.1039/C7SM01558E ↗
54. 10.1038/nmat256410.1038/nmat2564 ↗
55. 10.1039/c3cc46161k10.1039/c3cc46161k ↗
56. 10.1021/jacs.6b0798510.1021/jacs.6b07985 ↗
57. 10.1039/C6CC00594B10.1039/C6CC00594B ↗
58. 10.1021/bm300826v10.1021/bm300826v ↗
59. 10.1021/am506337610.1021/am5063376 ↗
60. 10.1002/adfm.20100073010.1002/adfm.201000730 ↗
61. 10.1039/C7TB01824J10.1039/C7TB01824J ↗
62. 10.1002/adma.20140423510.1002/adma.201404235 ↗
63. 10.1021/acs.analchem.5b0166910.1021/acs.analchem.5b01669 ↗
64. 10.1016/j.jcis.2014.07.03110.1016/j.jcis.2014.07.031 ↗
65. 10.1002/smll.20160273010.1002/smll.201602730 ↗
66. 10.1021/nl504997q10.1021/nl504997q ↗
67. 10.1016/j.bios.2011.04.04710.1016/j.bios.2011.04.047 ↗
68. 10.1016/j.bios.2016.03.01310.1016/j.bios.2016.03.013 ↗
69. 10.1021/la403598s10.1021/la403598s ↗
70. 10.1021/acs.langmuir.5b0349710.1021/acs.langmuir.5b03497 ↗
71. 10.1021/la200114s10.1021/la200114s ↗
72. 10.1021/bm501034910.1021/bm5010349 ↗