Near-Surface Oxidized Sulfur Modifications and Self-Assembly of Thiol-Modified Aptamer on Au Thin Film Substrates Influenced by Piranha Treatment
Source abstract
Abstract
Self-assembly of thiol-modified oligonucleotides on Au films has great importance for biosensor applications. Prior to the self-assembly, a piranha treatment (PT) is commonly used to clean the Au surface. Here we report that near-surface oxidized sulfur modifications on Au thin films by PT for longer than 60 s have serious effects on the self-assembled monolayer (SAM) formation of thiol-modified single-stranded thrombin binding aptamer (s-TBA), and a PT time of 10-30 s is optimal for s-TBA SAM formation. These results have important implication to SAM formation of biomolecules, especially for the thiol-modified ones where a careful consideration of this key step could significantly enhance the SAM formation and biosensor performance.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced biosensing and bioanalysis techniques · Molecular Junctions and Nanostructures · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
WATLab and Department of Chemistry, University of Waterloo, Waterloo, Ontario, Canada N2L3G1
References (31)
Show source-provided references
1. Xiao Y. · Angew. Chem., Int. Ed. · 2005 · 44 · 545610.1002/anie.200500989 ↗
2. Love J. C. · Chem. Rev. · 2005 · 105 · 110310.1021/cr0300789 ↗
3. Petrovykh D. Y. · J. Am. Chem. Soc. · 2003 · 125 · 521910.1021/ja029450c ↗
4. Cho H. · Nano Lett. · 2008 · 8 · 438610.1021/nl802245w ↗
5. Mairal T. · Anal. Bioanal. Chem. · 2008 · 390 · 98910.1007/s00216-007-1346-4 ↗
6. Huajun Q. · Colloids Surf., B · 2010 · 79 · 30410.1016/j.colsurfb.2010.04.017 ↗
7. Balamurugan S. · Langmuir · 2006 · 22 · 644610.1021/la060222w ↗
8. Radi A. E. · J. Am. Chem. Soc. · 2006 · 128 · 11710.1021/ja053121d ↗
9. Du Y. · Anal. Chem. · 2008 · 80 · 511010.1021/ac800303c ↗
10. Bock L. C. · Nature · 1992 · 355 · 56410.1038/355564a0 ↗
11. Lu Y. · Anal. Chem. · 2008 · 80 · 188310.1021/ac7018014 ↗
12. Li T. · Chem. Commun. · 2008 · 31 · 365410.1039/b805565c ↗
13. Opdahl A. · Proc. Natl. Acad. Sci. · 2007 · 104 · 910.1073/pnas.0608568103 ↗
14. Saha K. · Chem. Rev. · 2012 · 112 · 273910.1021/cr2001178 ↗
15. Tabor R. F. · Langmuir · 2011 · 27 · 602610.1021/la200166r ↗
16. Ron H. · Langmuir · 1994 · 10 · 456610.1021/la00024a030 ↗
17. Sun Y. · J. Mater. Chem. · 2011 · 21 · 1667510.1039/c1jm11640a ↗
18. Ansar S. M. · J. Phys. Chem. Lett. · 2012 · 3 · 56010.1021/jz2016439 ↗
19. Herne T. M. · J. Am. Chem. Soc. · 1997 · 119 · 891610.1021/ja9719586 ↗
20. Hoshiya N. · J. Am. Chem. Soc. · 2010 · 132 · 727010.1021/ja9100084 ↗
21. Day B. S. · Langmuir · 2011 · 27 · 1243410.1021/la202444s ↗
22. Guo L. H. · Langmuir · 1994 · 10 · 458810.1021/la00024a033 ↗
23. Kang J. · Langmuir · 2007 · 23 · 50910.1021/la0518804 ↗
24. He X. P. · J. Am. Chem. Soc. · 2011 · 133 · 364910.1021/ja110478j ↗
25. Feng G. · Analyst · 2011 · 136 · 505810.1039/c1an15642j ↗
26. Donavan K. C. · Anal. Chem. · 2011 · 83 · 242010.1021/ac2000835 ↗
27. Juodkazis K. · Electrochem. Commun. · 2000 · 2 · 50310.1016/S1388-2481(00)00069-2 ↗
28. Cook K. M. · Chem. Commun. · 2011 · 47 · 1255010.1039/c1cc15742f ↗
29. Mekhalif Z. · Langmuir · 1997 · 13 · 228510.1021/la960528a ↗
30. Dietrich M. P. · Langmuir · 2011 · 27 · 480810.1021/la104038q ↗
31. Petrovykh D. Y. · Langmuir · 2004 · 20 · 42910.1021/la034944o ↗