Fabrication of Antibody Microarrays by Light-Induced Covalent and Oriented Immobilization
Source abstract
Abstract
Antibody microarrays have important applications for the sensitive detection of biologically important target molecules and as biosensors for clinical applications. Microarrays produced by oriented immobilization of antibodies generally have higher antigen-binding capacities than those in which antibodies are immobilized with random orientations. Here, we present a UV photo-cross-linking approach that utilizes boronic acid to achieve oriented immobilization of an antibody on a surface while retaining the antigen-binding activity of the immobilized antibody. A photoactive boronic acid probe was designed and synthesized in which boronic acid provided good affinity and specificity for the recognition of glycan chains on the Fc region of the antibody, enabling covalent tethering to the antibody upon exposure to UV light. Once irradiated with optimal UV exposure (16 mW/cm(2)), significant antibody immobilization on a boronic acid-presenting surface with maximal antigen detection sensitivity in a single step was achieved, thus obviating the necessity of prior antibody modifications. The developed approach is highly modular, as demonstrated by its implementation in sensitive sandwich immunoassays for the protein analytes Ricinus communis agglutinin 120, human prostate-specific antigen, and interleukin-6 with limits of detection of 7.4, 29, and 16 pM, respectively. Furthermore, the present system enabled the detection of multiple analytes in samples without any noticeable cross-reactivities. Antibody coupling via the use of boronic acid and UV light represents a practical, oriented immobilization method with significant implications for the construction of a large array of immunosensors for diagnostic applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Biosensing Techniques and Applications · Monoclonal and Polyclonal Antibodies Research · Advanced biosensing and bioanalysis techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, National Tsing Hua University, Hsinchu 300, Taiwan
References (39)
Show source-provided references
1. Jonkheijm P. · Angew. Chem., Int. Ed. · 2008 · 47 · 961810.1002/anie.200801711 ↗
2. Lin P.-C. · Angew. Chem., Int. Ed. · 2006 · 45 · 428610.1002/anie.200600756 ↗
3. Fung E. T. · Curr. Opin. Biotechnol. · 2001 · 12 · 6510.1016/S0958-1669(00)00167-1 ↗
4. Haab B. B. · Curr. Opin. Biotechnol. · 2006 · 17 · 41510.1016/j.copbio.2006.06.013 ↗
5. Jung Y. · Analyst · 2008 · 133 · 69710.1039/b800014j ↗
6. Trilling A. K. · Analyst · 2013 · 138 · 161910.1039/c2an36787d ↗
7. O’Shannessy D. J. · J. Immunol. Methods · 1987 · 99 · 15310.1016/0022-1759(87)90120-7 ↗
8. Hage D. S. · Bioconjugate Chem. · 1997 · 8 · 91410.1021/bc970112o ↗
9. Abraham R. · J. Immunol. Methods · 1991 · 144 · 7710.1016/0022-1759(91)90233-6 ↗
10. Gao D. · J. Am. Chem. Soc. · 2006 · 128 · 67610.1021/ja056364e ↗
11. Jung Y. · Anal. Chem. · 2007 · 79 · 653410.1021/ac070484i ↗
12. Niu Y. · Langmuir · 2012 · 28 · 1771810.1021/la303032f ↗
13. Seo J.-S. · J. Am. Chem. Soc. · 2013 · 135 · 897310.1021/ja402447g ↗
14. James, T. D.InBoronic Acids Preparation, Applications in Organic Synthesis and Medicine;Hall, D. G., Ed.Wiley-VCH:Weinheim, Germany, 2005; pp441–479.
15. Springsteen G. · Tetrahedron · 2002 · 58 · 529110.1016/S0040-4020(02)00489-1 ↗
16. Guo Z. · Chem. Commun. · 2012 · 48 · 595610.1039/c2cc31985c ↗
17. Anslyn E. V. · J. Org. Chem. · 2007 · 72 · 68710.1021/jo0617971 ↗
18. Ellis G. A. · J. Am. Chem. Soc. · 2012 · 134 · 363110.1021/ja210719s ↗
19. Deshayes S. · J. Am. Chem. Soc. · 2013 · 135 · 1550110.1021/ja406406h ↗
20. Liu X.-C. · Chin. J. Chromatogr. · 2006 · 24 · 7310.1016/S1872-2059(06)60004-7 ↗
21. Liu X.-C. · J. Mol. Recognit. · 1996 · 9 · 46210.1002/(SICI)1099-1352(199634/12)9:5/6<462::AID-JMR283>3.0.CO;2-G ↗
22. Sorensen M. D. · Angew. Chem., Int. Ed. · 2007 · 46 · 240310.1002/anie.200604936 ↗
23. Yang Y.-L. · ACS Chem. Biol. · 2014 · 9 · 39010.1021/cb400631w ↗
24. Chen M.-L. · Angew. Chem., Int. Ed. · 2008 · 45 · 862710.1002/anie.200803377 ↗
25. Hsiao H.-Y. · Chem. Commun. · 2011 · 47 · 118710.1039/C0CC03816D ↗
26. Lin P.-C. · Anal. Chem. · 2009 · 81 · 877410.1021/ac9012122 ↗
27. Ho J.-A. · Biosens. Bioelectron. · 2010 · 26 · 102110.1016/j.bios.2010.08.048 ↗
28. Liu S. · Clin. Chim. Acta · 2008 · 395 · 5110.1016/j.cca.2008.04.031 ↗
29. Abad J. M. · J. Am. Chem. Soc. · 2002 · 124 · 1284510.1021/ja026658p ↗
30. Hashimoto M. · Eur. J. Org. Chem. · 2008 · 251310.1002/ejoc.200701069 ↗
31. Tanaka Y. · J. Am. Chem. Soc. · 2008 · 130 · 327810.1021/ja7109772 ↗
32. Chang T.-C. · Bioconjugate Chem. · 2013 · 24 · 189510.1021/bc400306g ↗
33. Jung Y. · Anal. Chem. · 2009 · 81 · 93610.1021/ac8014565 ↗
34. Narla S. N. · Lab Chip · 2012 · 12 · 165610.1039/c2lc21224b ↗
35. Xing Z. · J. Clin. Invest. · 1998 · 101 · 31110.1172/JCI1368 ↗
36. Savage P. · Eur. J. Cancer · 1996 · 32 · 109710.1016/0959-8049(96)00098-6 ↗
37. Black M. H. · Clin. Chem. · 1999 · 45 · 34710.1093/clinchem/45.3.347 ↗
38. Peppard J. V. · J. Immunol. Methods · 1992 · 148 · 2310.1016/0022-1759(92)90154-L ↗
39. Ida N. · J. Immunol. Methods · 1990 · 133 · 27910.1016/0022-1759(90)90369-7 ↗