journal article·2018-05-30

Self-Assembled N-Heterocyclic Carbene-Based Carboxymethylated Dextran Monolayers on Gold as a Tunable Platform for Designing Affinity-Capture Biosensor Surfaces

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

ACS Applied Materials & Interfaces· Volume 10· Issue 21
Publisher page

Abstract

Sensor surfaces play a predominant role in the development of optical biosensor technologies for the analysis of biomolecular interactions. Thiol-based self-assembled monolayers (SAMs) on gold have been widely used as linker layers for sensor surfaces. However, the degradation of the thiol-gold bond can limit the performance and durability of such surfaces, directly impacting their performance and cost-effectiveness. To this end, a new family of materials based on N-heterocyclic carbenes (NHCs) has emerged as an alternative for surface modification, capable of self-assembling onto a gold surface with higher affinity and superior stability as compared to the thiol-based systems. Here we demonstrate three applications of NHC SAMs supporting a dextran layer as a tunable platform for developing various affinity-capture biosensor surfaces. We describe the development and testing of NHC-based dextran biosensor surfaces modified with each of streptavidin, nitrilotriacetic acid, and recombinant Protein A. These affinity-capture sensor surfaces enable oriented binding of ligands for optimal performance in biomolecular assays. Together, the intrinsic high stability and flexible design of the NHC biosensing platforms show great promise and open up exciting possibilities for future biosensing applications.
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Research context

OpenAlex topics: N-Heterocyclic Carbenes in Organic and Inorganic Chemistry · Molecular Junctions and Nanostructures · Synthesis and properties of polymers

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

China University of Political Science and Law · Government of Canada · Ministry of Public Security of the People's Republic of China · Opening Project Fund of Shanghai Key Laboratory of Criminal Scene Evidence

References (44)

Show source-provided references
1. 10.1016/j.ccr.2004.05.01310.1016/j.ccr.2004.05.013 ↗
2. 10.1038/nature1338410.1038/nature13384 ↗
3. 10.1021/ja401965d10.1021/ja401965d ↗
4. 10.1038/nchem.189110.1038/nchem.1891 ↗
5. 10.1038/ncomms1265410.1038/ncomms12654 ↗
6. 10.1038/nchem.262210.1038/nchem.2622 ↗
7. 10.1021/acs.chemrev.5b0022010.1021/acs.chemrev.5b00220 ↗
8. 10.1039/C7CS00023E10.1039/C7CS00023E ↗
9. 10.1021/acs.langmuir.7b0328010.1021/acs.langmuir.7b03280 ↗
10. 10.1021/acsami.7b1311410.1021/acsami.7b13114 ↗
11. 10.1021/acssensors.6b0076310.1021/acssensors.6b00763 ↗
12. Schasfoort R. B. M. · 2008
13. 2008
14. Cooper M. A. · 200910.1017/CBO9780511626531 ↗
15. 10.1038/nrd83810.1038/nrd838 ↗
16. 1998
17. 10.1007/s00216-003-2111-y10.1007/s00216-003-2111-y ↗
18. 10.1016/0022-1759(95)00032-610.1016/0022-1759(95)00032-6 ↗
19. 10.1006/abio.1997.232610.1006/abio.1997.2326 ↗
20. 10.1002/jmr.94110.1002/jmr.941 ↗
21. 10.1016/S0956-5663(99)00032-910.1016/S0956-5663(99)00032-9 ↗
22. 10.1039/an996210029r10.1039/an996210029r ↗
23. 10.1093/abbs/gmp02210.1093/abbs/gmp022 ↗
24. 10.1073/pnas.150215911210.1073/pnas.1502159112 ↗
25. 10.1073/pnas.110684010810.1073/pnas.1106840108 ↗
26. 10.1038/srep1647010.1038/srep16470 ↗
27. 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 ↗
28. 10.1039/C6CC00095A10.1039/C6CC00095A ↗
29. 10.1021/jacs.5b1093910.1021/jacs.5b10939 ↗
30. 10.1016/j.bios.2016.04.09110.1016/j.bios.2016.04.091 ↗
31. 10.1021/acs.analchem.5b0467910.1021/acs.analchem.5b04679 ↗
32. 10.1093/nar/30.10.e4510.1093/nar/30.10.e45 ↗
33. 10.1016/j.bios.2016.02.00310.1016/j.bios.2016.02.003 ↗
34. 10.1021/bi061903t10.1021/bi061903t ↗
35. 10.1016/j.snb.2010.08.01410.1016/j.snb.2010.08.014 ↗
36. 10.1021/bi201226e10.1021/bi201226e ↗
37. 10.1021/bi300228n10.1021/bi300228n ↗
38. Marquart, J. A. Surface Plasmon Resonance and Biomolecular Interaction Analysis: Theory and Practice, 4th ed; 2013.
39. 2014
40. 10.1016/j.trac.2016.02.00610.1016/j.trac.2016.02.006 ↗
41. 10.1088/0022-3727/40/23/S0210.1088/0022-3727/40/23/S02 ↗
42. 10.1039/c2an36787d10.1039/c2an36787d ↗
43. 10.1016/j.chroma.2016.01.02210.1016/j.chroma.2016.01.022 ↗
44. 10.1016/j.chroma.2015.08.06810.1016/j.chroma.2015.08.068 ↗