journal article·2022-02-25

DNA-Functionalized Ti3C2Tx MXenes for Selective and Rapid Detection of SARS-CoV-2 Nucleocapsid Gene

Winston Yenyu Chen, Hang Lin, Amit Kumar Barui, Ana Maria Ulloa Gomez, Michael K. Wendt, Lia A. Stanciu

ACS Applied Nano Materials· Volume 5· Issue 2
Publisher page

Abstract

Coronavirus disease 2019 (COVID-19) is an emerging human infectious disease caused by severe acute respiratory syndrome 2 (SARS-CoV-2, initially called novel coronavirus 2019-nCoV) virus. Thus, an accurate and specific diagnosis of COVID-19 is urgently needed for effective point-of-care detection and disease management. The reported promise of two-dimensional (2D) transition-metal carbides (Ti3C2Tx MXene) for biosensing owing to a very high surface area, high electrical conductivity, and hydrophilicity informed their selection for inclusion in functional electrodes for SARS-CoV-2 detection. Here, we demonstrate a new and facile functionalization strategy for Ti3C2Tx with probe DNA molecules through noncovalent adsorption, which eliminates expensive labeling steps and achieves sequence-specific recognition. The 2D Ti3C2Tx functionalized with complementary DNA probes shows a sensitive and selective detection of nucleocapsid (N) gene from SARS-CoV-2 through nucleic acid hybridization and chemoresistive transduction. The fabricated sensors are able to detect the SARS-CoV-2 N gene with sensitive and rapid response, a detection limit below 105 copies/mL in saliva, and high specificity when tested against SARS-CoV-1 and MERS. We hypothesize that the MXenes’ interlayer spacing can serve as molecular sieving channels for hosting organic molecules and ions, which is a key advantage to their use in biomolecular sensing.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: MXene and MAX Phase Materials · Advanced biosensing and bioanalysis techniques · Energy Harvesting in Wireless Networks

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

Affiliations

School of Materials Engineering, Purdue University, West Lafayette, Indiana 47907, United States

Birck Nanotechnology Center, Purdue University, West Lafayette, Indiana 47907 United States

Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, Indiana 47907 United States

Purdue Center for Cancer Research, Purdue University, West Lafayette, Indiana 47907 United States

Funding

Division of Chemical, Bioengineering, Environmental, and Transport Systems

References (60)

Show source-provided references
1. Coronavirus disease 2019. COVID-19 Situation Report; World Health Organization, 2020.
2. 10.2807/1560-7917.ES.2020.25.3.200004510.2807/1560-7917.ES.2020.25.3.2000045 ↗
3. 10.2807/1560-7917.ES.2020.25.24.200105710.2807/1560-7917.ES.2020.25.24.2001057 ↗
4. 10.1021/acsnano.0c0262410.1021/acsnano.0c02624 ↗
5. 10.1021/acssensors.0c0118010.1021/acssensors.0c01180 ↗
6. 10.1021/acsnano.0c0243910.1021/acsnano.0c02439 ↗
7. 10.1021/acsnano.0c0282310.1021/acsnano.0c02823 ↗
8. 10.1021/acs.nanolett.1c0011810.1021/acs.nanolett.1c00118 ↗
9. 10.1021/jacs.0c1081010.1021/jacs.0c10810 ↗
10. 10.1016/j.bios.2020.11243610.1016/j.bios.2020.112436 ↗
11. 10.1002/adma.20140108410.1002/adma.201401084 ↗
12. 10.1021/acs.nanolett.8b0381810.1021/acs.nanolett.8b03818 ↗
13. 10.1021/acs.langmuir.6b0450210.1021/acs.langmuir.6b04502 ↗
14. 10.1002/adma.20110230610.1002/adma.201102306 ↗
15. 10.1038/natrevmats.2016.9810.1038/natrevmats.2016.98 ↗
16. 10.1021/acsnano.0c0548210.1021/acsnano.0c05482 ↗
17. 10.1039/C8CS00324F10.1039/C8CS00324F ↗
18. 10.1002/adfm.20180197210.1002/adfm.201801972 ↗
19. 10.1016/j.mattod.2019.05.01710.1016/j.mattod.2019.05.017 ↗
20. 10.1016/j.chempr.2018.08.03710.1016/j.chempr.2018.08.037 ↗
21. 10.1021/acsnano.9b0639410.1021/acsnano.9b06394 ↗
22. 10.1021/acs.analchem.8b0308310.1021/acs.analchem.8b03083 ↗
23. 10.1021/acs.analchem.1c0037110.1021/acs.analchem.1c00371 ↗
24. 10.1002/advs.20180051810.1002/advs.201800518 ↗
25. 10.1016/j.tibtech.2019.09.00110.1016/j.tibtech.2019.09.001 ↗
26. 10.1021/acsnano.0c0959510.1021/acsnano.0c09595 ↗
27. 10.1038/ncomms1490210.1038/ncomms14902 ↗
28. 10.1021/acsnano.7b0746010.1021/acsnano.7b07460 ↗
29. 10.1002/adfm.20090163910.1002/adfm.200901639 ↗
30. 10.1039/C9SC03049B10.1039/C9SC03049B ↗
31. 10.1002/nano.20200030910.1002/nano.202000309 ↗
32. 10.1021/acs.analchem.0c0078410.1021/acs.analchem.0c00784 ↗
33. 10.1016/j.bios.2019.11153110.1016/j.bios.2019.111531 ↗
34. 10.1021/acs.accounts.7b0048110.1021/acs.accounts.7b00481 ↗
35. 10.1038/s41467-017-02529-610.1038/s41467-017-02529-6 ↗
36. 10.1039/D1TA03070A10.1039/D1TA03070A ↗
37. 10.1039/C7TA11347A10.1039/C7TA11347A ↗
38. 10.1021/acs.chemmater.7b0284710.1021/acs.chemmater.7b02847 ↗
39. 10.1021/acsami.5b1197310.1021/acsami.5b11973 ↗
40. 10.1021/cm500641a10.1021/cm500641a ↗
41. 10.1039/C6CC07733A10.1039/C6CC07733A ↗
42. 10.1021/ja971958610.1021/ja9719586 ↗
43. 10.1016/S0140-6736(20)30251-810.1016/S0140-6736(20)30251-8 ↗
44. 10.1073/pnas.200313811710.1073/pnas.2003138117 ↗
45. Walls A. C. · Cell · 2020 · 181 · 28110.1016/j.cell.2020.02.058 ↗
46. 10.1016/j.cell.2020.06.04310.1016/j.cell.2020.06.043 ↗
47. 10.1128/JVI.00647-2010.1128/JVI.00647-20 ↗
48. 10.1126/science.108641810.1126/science.1086418 ↗
49. 10.1128/JVI.01925-1910.1128/JVI.01925-19 ↗
50. 10.1093/cid/ciaa138210.1093/cid/ciaa1382 ↗
51. 10.1001/jamainternmed.2020.887610.1001/jamainternmed.2020.8876 ↗
52. 10.1021/acssensors.9b0030310.1021/acssensors.9b00303 ↗
53. 10.1038/s41467-020-18611-510.1038/s41467-020-18611-5 ↗
54. 10.1021/acsnano.0c0442110.1021/acsnano.0c04421 ↗
55. 10.1021/acs.analchem.5b0159410.1021/acs.analchem.5b01594 ↗
56. 10.1056/NEJMc151169510.1056/NEJMc1511695 ↗
57. 10.1056/NEJMc200173710.1056/NEJMc2001737 ↗
58. 10.1016/j.jinf.2020.06.06710.1016/j.jinf.2020.06.067 ↗
59. Prevention, U. C. f.D. C. A., 2019-Novel Coronavirus (2019-nCoV) Real-time rRT-PCR Primers and Probes, 2020.
60. 10.1021/acsnano.0c0389610.1021/acsnano.0c03896 ↗