journal article·2019-08-21

Specific and Quantitative Detection of Albumin in Biological Fluids by Tetrazolate-Functionalized Water-Soluble AIEgens

Yujie Tu, Yeqing Yu, Zhibiao Zhou, Sheng Xie, Bicheng Yao, Shujuan Guan, Bo Situ, Yong Liu, Ryan T. K. Kwok, Jacky W. Y. Lam, Sijie Chen, Xuhui Huang, Zebing Zeng, Ben Zhong Tang

ACS Applied Materials & Interfaces· Volume 11· Issue 33
Publisher page

Abstract

The analysis of albumin has clinical significance in diagnostic tests and obvious value to research studies on the albumin-mediated drug delivery and therapeutics. The present immunoassay, instrumental techniques, and colorimetric methods for albumin detection are either expensive, troublesome, or insensitive. Herein, a class of water-soluble tetrazolate-functionalized derivatives with aggregation-induced emission (AIE) characteristics is introduced as novel fluorescent probes for albumin detection. They can be selectively lighted up by site-specific binding with albumin. The resulting albumin fluorescent assay exhibits a low detection limit (0.21 nM), high robustness in aqueous buffer (pH = 6–9), and a broad tunable linear dynamic range (0.02–3000 mg/L) for quantification. The tetrazolate functionality endows the probes with a superior water solubility (>0.01 M) and a high binding affinity to albumin (KD = 0.25 μM). To explore the detection mechanism, three unique polar binding sites on albumin are computationally identified, where the multivalent tetrazolate–lysine interactions contribute to the tight binding and restriction of the molecular motion of the AIE probes. The key role of lysine residues is verified by the detection of poly-l-lysine. Moreover, we applied the fluorogenic method to quantify urinary albumin in clinical samples and found it a feasible and practical strategy for albumin analysis in complex biological fluids.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced biosensing and bioanalysis techniques · Lipid Membrane Structure and Behavior · Advanced Biosensing Techniques and Applications

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

Affiliations

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China

Department of Laboratory Medicine, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China

Ming Wai Lau Center for Reparative Medicine, Karolinska Institutet, Hong Kong 999077, China

State Key Laboratory of Luminescent Materials and Devices, Center for Aggregation-Induced Emission, (Guangzhou International Campus), South China University of Technology, Guangzhou 510640, China

Funding

Research Grants Council, University Grants Committee · Ministry of Science and Technology of the People's Republic of China · Innovation and Technology Commission · National Natural Science Foundation of China · AIEgen Biotech Co. Ltd

References (80)

Show source-provided references
1. 10.1016/j.mam.2011.12.00210.1016/j.mam.2011.12.002 ↗
2. 10.1016/j.tmrv.2009.09.00510.1016/j.tmrv.2009.09.005 ↗
3. 10.1007/s11739-012-0802-010.1007/s11739-012-0802-0 ↗
4. 10.1016/j.amjmed.2017.07.02010.1016/j.amjmed.2017.07.020 ↗
5. 10.1309/972n441wgkprtmrk10.1309/972n441wgkprtmrk ↗
6. 10.1016/j.tmrv.2009.09.00510.1016/j.tmrv.2009.09.005 ↗
7. 10.1001/jama.2015.060210.1001/jama.2015.0602 ↗
8. 10.1016/j.cca.2017.04.00710.1016/j.cca.2017.04.007 ↗
9. 10.1186/s40591-016-0048-810.1186/s40591-016-0048-8 ↗
10. 10.7150/thno.1936510.7150/thno.19365 ↗
11. 10.1016/j.addr.2018.07.01110.1016/j.addr.2018.07.011 ↗
12. 10.1016/j.drudis.2018.01.05110.1016/j.drudis.2018.01.051 ↗
13. 10.1021/ja302363r10.1021/ja302363r ↗
14. 10.1002/cmdc.20160008010.1002/cmdc.201600080 ↗
15. 10.1021/jacs.7b0291710.1021/jacs.7b02917 ↗
16. 10.1038/s41467-017-02191-y10.1038/s41467-017-02191-y ↗
17. 10.1002/anie.20180415610.1002/anie.201804156 ↗
18. 10.1021/jacs.8b0601110.1021/jacs.8b06011 ↗
19. 10.1038/s41467-019-10056-910.1038/s41467-019-10056-9 ↗
20. 10.1002/adfm.20190271710.1002/adfm.201902717 ↗
21. 10.1053/j.tcam.2011.04.00210.1053/j.tcam.2011.04.002 ↗
22. 10.1006/abio.1976.999910.1006/abio.1976.9999 ↗
23. Lowry O. H. · J Biol Chem · 1951 · 193 · 26510.1016/S0021-9258(19)52451-6 ↗
24. Eckfeldt JH · Clin Chem · 1984 · 30 · 44310.1093/clinchem/30.3.443 ↗
25. 10.1016/s0009-9120(85)80033-310.1016/s0009-9120(85)80033-3 ↗
26. 10.1021/cr300508p10.1021/cr300508p ↗
27. 10.1021/acs.accounts.6b0051710.1021/acs.accounts.6b00517 ↗
28. 10.1039/c7cs00907k10.1039/c7cs00907k ↗
29. 10.1039/c1an15255f10.1039/c1an15255f ↗
30. 10.1016/j.aca.2017.07.04810.1016/j.aca.2017.07.048 ↗
31. 10.1016/j.snb.2017.02.04610.1016/j.snb.2017.02.046 ↗
32. 10.1016/j.dyepig.2016.05.03910.1016/j.dyepig.2016.05.039 ↗
33. 10.1039/c5cc08217j10.1039/c5cc08217j ↗
34. 10.1002/hc.2137110.1002/hc.21371 ↗
35. 10.1016/j.tetlet.2018.02.06510.1016/j.tetlet.2018.02.065 ↗
36. 10.1016/j.dyepig.2018.01.03310.1016/j.dyepig.2018.01.033 ↗
37. 10.1021/acs.analchem.8b0118110.1021/acs.analchem.8b01181 ↗
38. 10.1021/ja061301x10.1021/ja061301x ↗
39. 10.1002/anie.20070024510.1002/anie.200700245 ↗
40. 10.1021/jp102953610.1021/jp1029536 ↗
41. 10.1016/j.jphotochem.2012.11.01310.1016/j.jphotochem.2012.11.013 ↗
42. 10.1021/ja503850b10.1021/ja503850b ↗
43. 10.1016/j.biomaterials.2013.10.03910.1016/j.biomaterials.2013.10.039 ↗
44. 10.1021/acs.chemrev.6b0000110.1021/acs.chemrev.6b00001 ↗
45. 10.1021/acs.analchem.6b0077410.1021/acs.analchem.6b00774 ↗
46. 10.1021/acs.analchem.7b0292310.1021/acs.analchem.7b02923 ↗
47. 10.1016/j.snb.2017.08.13210.1016/j.snb.2017.08.132 ↗
48. Kessler MA · Clin Chem · 1992 · 38 · 208910.1093/clinchem/38.10.2089 ↗
49. Kessler M. A. · Clin. Chem. · 1997 · 43 · 99610.1093/clinchem/43.6.996 ↗
50. 10.1006/abio.1997.211310.1006/abio.1997.2113 ↗
51. 10.1039/c4cs00325j10.1039/c4cs00325j ↗
52. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
53. 10.1002/chem.20180529710.1002/chem.201805297 ↗
54. 10.1021/ac101802810.1021/ac1018028 ↗
55. 10.1007/s11426-013-4917-610.1007/s11426-013-4917-6 ↗
56. 10.1016/j.snb.2016.12.05410.1016/j.snb.2016.12.054 ↗
57. 10.1021/acsami.5b0742210.1021/acsami.5b07422 ↗
58. 10.1039/b608425g10.1039/b608425g ↗
59. 10.1039/c1cc15735c10.1039/c1cc15735c ↗
60. 10.1039/c6fd00165c10.1039/c6fd00165c ↗
61. Cambridge MedChem Consulting. https://www.cambridgemedchemconsulting.com/resources/bioisoteres/acid_bioisosteres.html (accessed Jan 16, 2019).
62. 10.1021/cr950066q10.1021/cr950066q ↗
63. 10.1007/s10847-013-0334-x10.1007/s10847-013-0334-x ↗
64. 10.1002/jcc.2133410.1002/jcc.21334 ↗
65. 10.1016/0263-7855(96)00018-510.1016/0263-7855(96)00018-5 ↗
66. 10.1016/j.softx.2015.06.00110.1016/j.softx.2015.06.001 ↗
67. Gaussian 09; Gaussian, Inc.: Wallingford CT, 2009. http://gaussian.com/glossary/g09/.
68. 10.1002/jcc.54005020410.1002/jcc.540050204 ↗
69. 10.1063/1.44586910.1063/1.445869 ↗
70. Sanborn, N. E.; Hayre, N. R.; Singh, R. R.; Cox, D. L. All-Atom Molecular Dynamics Simulations of the Projection Domain of the Intrinsically Disordered Htau40 Protein. 2016, arXiv preprint arXiv:1610.09696.
71. 10.1063/1.46439710.1063/1.464397 ↗
72. 10.1063/1.47011710.1063/1.470117 ↗
73. 10.1063/1.240842010.1063/1.2408420 ↗
74. 10.1063/1.44811810.1063/1.448118 ↗
75. 10.1021/ci500020m10.1021/ci500020m ↗
76. 10.1002/anie.20180165310.1002/anie.201801653 ↗
77. 10.1002/jmr.116710.1002/jmr.1167 ↗
78. 10.2174/13895570677636144810.2174/138955706776361448 ↗
79. 10.1016/j.bpc.2010.03.00110.1016/j.bpc.2010.03.001 ↗
80. 10.1016/j.ijbiomac.2016.03.03010.1016/j.ijbiomac.2016.03.030 ↗