journal article·2008-04-01

Temperature-Responsive Self-Assembled Monolayers of Oligo(ethylene glycol): Control of Biomolecular Recognition

Hadi M. Zareie, Cyrille Boyer, Volga Bulmus, Ebrahim Nateghi, Thomas P. Davis

ACS Nano· Volume 2· Issue 4
Publisher page

Abstract

Self-assembled monolayers (SAMs) of oligo(ethylene glycol) (OEG)-tethered molecules on gold are important for various biorelevant applications ranging from biomaterials to bioanalytical devices, where surface resistance to nonspecific protein adsorption is needed. Incorporation of a stimuli-responsive character to the OEG SAMs enables the creation of nonfouling surfaces with switchable functionality. Here we present an OEG-derived structure that is highly responsive to temperature changes in the vicinity of the physiological temperature, 37 degrees C. The temperature-responsive solution behavior of this new compound was demonstrated by UV-vis and nuclear magnetic resonance spectroscopy. Its chemisorption onto gold(111), and the retention of responsive behavior after chemisorption have been demonstrated by surface plasmon resonance (SPR), X-ray photoelectron spectroscopy (XPS), and atomic force and scanning tunneling microscopy. The OEG-derived SAMs have been shown to reversibly switch the wettability of the surface, as determined by contact angle measurements. More importantly, SPR and AFM studies showed that the OEG SAMs can be utilized to control the affinity binding of streptavidin to the biotin-tethered surface in a temperature-dependent manner while still offering the nonspecific protein-resistance to the surface.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Molecular Junctions and Nanostructures · Advanced biosensing and bioanalysis techniques · Supramolecular Self-Assembly in Materials

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

Affiliations

Institute for Nanoscale Technology, University of Technology, Sydney (UTS), Sydney 2007, Australia

Centre for Advanced Macromolecular Design (CAMD), School of Chemical Sciences and Engineering

School of Biotechnology and Biomolecular Sciences (BABS), The University of New South Wales (UNSW), Sydney 2034, NSW Australia

References (64)

Show source-provided references
1. Love J. C. · Chem. Rev. · 2005 · 105 · 110310.1021/cr0300789 ↗
2. Nuzzo R. · Nat. Mater. · 2003 · 2 · 20710.1038/nmat872 ↗
3. Bearinger J. P. · Nat. Mater. · 2003 · 2 · 25910.1038/nmat851 ↗
4. Whitesides G. M. · Annu. Rev. Biomed. Eng. · 2001 · 3 · 33510.1146/annurev.bioeng.3.1.335 ↗
5. Prime K. L. · Science · 1991 · 252 · 116410.1126/science.252.5009.1164 ↗
6. Prime K. L. · J. Am. Chem. Soc. · 1993 · 115 · 1071410.1021/ja00076a032 ↗
7. Zhen G. L. · Adv. Funct. Mater. · 2006 · 16 · 24310.1002/adfm.200500232 ↗
8. Lata S. · Anal. Chem. · 2005 · 77 · 109610.1021/ac048813j ↗
9. Zhen G. · Langmuir · 2004 · 20 · 1046410.1021/la0482812 ↗
10. Falconnet D. · Adv. Funct. Mater. · 2004 · 14 · 74910.1002/adfm.200305182 ↗
11. Falconnet D. · Nano Lett. · 2004 · 4 · 190910.1021/nl0489438 ↗
12. Cha T. · Proteomics · 2004 · 4 · 196510.1002/pmic.200300747 ↗
13. Lee J. K. · J. Phys. Chem. B · 2004 · 108 · 766510.1021/jp0378236 ↗
14. Pasche S. · Langmuir · 2003 · 19 · 921610.1021/la034111y ↗
15. Huang N. P. · Langmuir · 2002 · 18 · 22010.1021/la010913m ↗
16. Huang N. P. · Langmuir · 2001 · 17 · 48910.1021/la000736+ ↗
17. Flynn N. T. · Langmuir · 2003 · 19 · 1090910.1021/la035331e ↗
18. Raynor J. E. · Adv. Mater. · 2007 · 19 · 172410.1002/adma.200602129 ↗
19. Faragher R. J. · J. Org. Chem. · 2008 · 73 · 137110.1021/jo701979z ↗
20. Herrwerth S. · J. Am. Chem. Soc. · 2003 · 125 · 935910.1021/ja034820y ↗
21. Schwendel D. · Langmuir · 2001 · 17 · 571710.1021/la010576h ↗
22. Khademhosseini A. · Adv. Mater. · 2003 · 15 · 199510.1002/adma.200305433 ↗
23. Wang R. L. C. · J. Phys. Chem. B · 1997 · 101 · 976710.1021/jp9716952 ↗
24. Wang R. L. C. · Phys. Chem. Chem. Phys. · 2000 · 2 · 361310.1039/b002593n ↗
25. Ionov L. · Nano Lett. · 2005 · 5 · 191010.1021/nl051235h ↗
26. Karlstrom G. · J. Phys. Chem. · 1985 · 89 · 496210.1021/j100269a015 ↗
27. Smith G. D. · J. Phys. Chem. B · 2003 · 107 · 309510.1021/jp0270046 ↗
28. Dormidontova E. E. · Macromolecules · 2004 · 37 · 774710.1021/ma035609+ ↗
29. Balamurugan S. · J. Am. Chem. Soc. · 2005 · 127 · 1454810.1021/ja054156g ↗
30. Cunliffe D. · Langmuir · 2003 · 19 · 288810.1021/la026358l ↗
31. Park E. J. · Langmuir · 2007 · 23 · 708310.1021/la700624g ↗
32. Pong F. Y. · Langmuir · 2006 · 22 · 385110.1021/la0534165 ↗
33. Cho E. C. · Polymer · 2004 · 45 · 319510.1016/j.polymer.2004.02.052 ↗
34. Zhu M. Q. · J. Am. Chem. Soc. · 2004 · 126 · 265610.1021/ja038544z ↗
35. Jones D. M. · Adv. Mater. · 2002 · 14 · 113010.1002/1521-4095(20020816)14:16<1130::AID-ADMA1130>3.0.CO;2-7 ↗
36. Cheng X. · Biointerphases · 2006 · 1 · 6110.1116/1.2187980 ↗
37. Valkama S. · Nat. Mater. · 2004 · 3 · 87210.1038/nmat1254 ↗
38. Hyun J. · J. Am. Chem. Soc. · 2004 · 126 · 733010.1021/ja049721e ↗
39. Mather P. T. · Nat. Mater. · 2007 · 6 · 9310.1038/nmat1834 ↗
40. Dexter A. F. · Nat. Mater. · 2006 · 5 · 50210.1038/nmat1653 ↗
41. Boyer C. · J. Am. Chem. Soc. · 2007 · 129 · 714510.1021/ja070956a ↗
42. Lutz J. F. · J. Am. Chem. Soc. · 2006 · 128 · 1304610.1021/ja065324n ↗
43. Fundueanu G. · Eur. Polym. J. · 2007 · 43 · 350010.1016/j.eurpolymj.2007.05.026 ↗
44. Feil H. · Macromolecules · 1993 · 26 · 249610.1021/ma00062a016 ↗
45. Kosik K. · J. Phys. Chem. B · 2008 · 112 · 106510.1021/jp075227w ↗
46. Francis R. · Polymer · 2007 · 48 · 670710.1016/j.polymer.2007.08.061 ↗
47. Dimitrov I. · Prog. Polym. Sci. · 2007 · 32 · 127510.1016/j.progpolymsci.2007.07.001 ↗
48. Biacore 2000 Handbook, version AB;Biacore: Uppsala, Sweden, 1998.
49. Jungs L. S. · Langmuir · 1998 · 14 · 563610.1021/la971228b ↗
50. Ulman A. · Chem. Rev. · 1996 · 96 · 153310.1021/cr9502357 ↗
51. Cao R. · J. Am. Chem. Soc. · 2007 · 129 · 692710.1021/ja068349v ↗
52. Kocharova N. · Langmuir · 2007 · 23 · 336310.1021/la0631522 ↗
53. Vance A. L. · Langmuir · 2002 · 18 · 812310.1021/la025631g ↗
54. Chen X. · Adv. Mater. Res. · 2006 · 11 · 36310.4028/www.scientific.net/AMR.11-12.363 ↗
55. Balamurugan S. · Langmuir · 2003 · 7 · 254510.1021/la026787j ↗
56. Nelson K. E. · Langmuir · 2001 · 17 · 280710.1021/la001111e ↗
57. Jung L. S. · Langmuir · 2000 · 16 · 942110.1021/la000144r ↗
58. Schwendel D. · Langmuir · 2001 · 17 · 571710.1021/la010576h ↗
59. Peres-Luna V. H. · J. Am. Chem. Soc. · 1999 · 121 · 646910.1021/ja983984p ↗
60. Xia N. · Langmuir · 2004 · 20 · 371010.1021/la035864n ↗
61. Waner M. J. · Biophys. J. · 2004 · 87 · 270110.1529/biophysj.104.047266 ↗
62. Gonzalez M. · Biomol. Eng. · 1999 · 16 · 6710.1016/S1050-3862(99)00041-8 ↗
63. Bayer E. A. · Electrophoresis · 1996 · 17 · 131910.1002/elps.1150170808 ↗
64. Beamson · 1992