journal article·2017-11-15

Carboxymethylated Dextran-Modified N-Heterocyclic Carbene Self-Assembled Monolayers on Gold for Use in Surface Plasmon Resonance Biosensing

Zhijun Li, Mina R. Narouz, Kim Munro, Bin Hao, Cathleen M. Crudden, J. Hugh Horton, Hongxia Hao

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Abstract

Surface chemistry is a key enabler for various biosensing applications. Biosensors based on surface plasmon resonance routinely employ thiol-based chemistry for the linker layer between gold-coated support surfaces and functional biosensor surfaces. However, there is a growing awareness that such sensor surfaces are prone to oxidation/degradation problems in the presence of oxygen, and previous efforts to improve the stability have shown limited advancements. As an alternative, recent studies employing N-heterocyclic carbene (NHC) self-assembled monolayers (SAMs) deposited on gold have shown significant promise in this area. Here, we describe a sensor surface employing an NHC SAM to couple a modified carboxymethylated dextran onto a gold surface. Such a dextran matrix is also used for affinity chromatography, and it is the most commonly employed matrix for commercial biosensor surfaces today. The performance reliability of the dextran-modified NHC chip to act as an alternative biosensing platform is compared with that of a thiol-based commercial chip in the proof-of-concept tests. The resultant NHC sensor surface shows a higher thermal stability compared to thiol analogues. Moreover, the plasma protein/drug and antibody/antigen interactions were validated on the NHC-based dextran chip and showed similar performance as compared to the thiol-based commercial chip. Ultimately, this study shows the strong potential applicability of chemical modifications to gold surfaces using NHC ligands for biosensing applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Molecular Junctions and Nanostructures · Advanced biosensing and bioanalysis techniques · Click Chemistry and Applications

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

Affiliations

Collaborative Innovation Center of Judicial Civilization and Key Laboratory of Evidence Science, China University of Political Science and Law, Beijing 100088, China

Institute for Transformative Bio-Molecules (ITbM-WPI), Nagoya University, Chikusa, Nagoya 464-8602, Japan

Funding

Beijing Municipal Commission of Education · China University of Political Science and Law · Natural Sciences and Engineering Research Council of Canada · Ministry of Public Security of the People?s Republic of China

References (54)

Show source-provided references
1. 10.1021/cr030078910.1021/cr0300789 ↗
2. 10.1039/c0cs00139b10.1039/c0cs00139b ↗
3. Schasfoort R. B. M. · 2008
4. Cooper M. A. · 200910.1017/CBO9780511626531 ↗
5. 10.1016/j.snb.2010.08.01410.1016/j.snb.2010.08.014 ↗
6. 10.1021/acssensors.6b0076310.1021/acssensors.6b00763 ↗
7. 10.1021/acs.chemrev.6b0022010.1021/acs.chemrev.6b00220 ↗
8. 10.1039/C3990000152610.1039/C39900001526 ↗
9. 10.1351/pac19956705082910.1351/pac199567050829 ↗
10. 10.1021/la404662210.1021/la4046622 ↗
11. 10.1021/ja00155a01610.1021/ja00155a016 ↗
12. 10.1039/b907301a10.1039/b907301a ↗
13. 10.1021/la800947z10.1021/la800947z ↗
14. 10.1021/la035331e10.1021/la035331e ↗
15. 10.1002/chem.20130211510.1002/chem.201302115 ↗
16. 10.1021/la980263v10.1021/la980263v ↗
17. 10.1038/nature1338410.1038/nature13384 ↗
18. 10.1038/nchem.189110.1038/nchem.1891 ↗
19. 10.1021/acs.chemrev.5b0022010.1021/acs.chemrev.5b00220 ↗
20. 10.1038/nchem.262210.1038/nchem.2622 ↗
21. 10.1038/ncomms1265410.1038/ncomms12654 ↗
22. 10.1021/acs.bioconjchem.6b0059810.1021/acs.bioconjchem.6b00598 ↗
23. 10.1021/acs.langmuir.6b0249610.1021/acs.langmuir.6b02496 ↗
24. 10.1002/chem.20150233310.1002/chem.201502333 ↗
25. 10.1021/ac400386z10.1021/ac400386z ↗
26. 10.1002/anie.20170160510.1002/anie.201701605 ↗
27. 10.1016/j.snb.2010.08.01410.1016/j.snb.2010.08.014 ↗
28. 10.1016/j.trac.2016.02.00610.1016/j.trac.2016.02.006 ↗
29. Van der Merwe P. A. · 2001
30. 1999
31. 10.1021/jm991174y10.1021/jm991174y ↗
32. 10.1002/(SICI)1099-1352(199909/10)12:5<279::AID-JMR473>3.0.CO;2-310.1002/(SICI)1099-1352(199909/10)12:5<279::AID-JMR473>3.0.CO;2-3 ↗
33. 10.1006/abio.2001.531410.1006/abio.2001.5314 ↗
34. 10.1016/j.colsurfb.2016.06.05710.1016/j.colsurfb.2016.06.057 ↗
35. 10.1021/bm060385z10.1021/bm060385z ↗
36. 10.1039/C3TB21732A10.1039/C3TB21732A ↗
37. 10.1016/j.carbpol.2006.08.02210.1016/j.carbpol.2006.08.022 ↗
38. 10.1016/j.elspec.2003.10.00510.1016/j.elspec.2003.10.005 ↗
39. 10.1021/ja00019a01110.1021/ja00019a011 ↗
40. 10.1021/ja028692+10.1021/ja028692+ ↗
41. 10.1021/ja401965d10.1021/ja401965d ↗
42. 10.1021/acs.langmuir.6b0145810.1021/acs.langmuir.6b01458 ↗
43. 10.1021/la951087i10.1021/la951087i ↗
44. 10.1016/S0142-9612(99)00270-710.1016/S0142-9612(99)00270-7 ↗
45. 10.1021/jp963899910.1021/jp9638999 ↗
46. Marquart J. A. · 2014
47. 10.1016/0021-9797(91)90043-810.1016/0021-9797(91)90043-8 ↗
48. 10.1021/ma400803j10.1021/ma400803j ↗
49. BIAevaluation 3.0 Software Handbook;Biacore AB, 1997.
50. 10.1021/ac500054x10.1021/ac500054x ↗
51. 10.1021/acs.analchem.6b0319210.1021/acs.analchem.6b03192 ↗
52. 10.1021/acs.analchem.6b0351110.1021/acs.analchem.6b03511 ↗
53. 10.1016/j.ab.2017.03.00310.1016/j.ab.2017.03.003 ↗
54. http://www.colby.edu/chemistry/PChem/lab/SPRBSAAntiBSA.pdf.