Click-Reaction-Triggered SERS Signals for Specific Detection of Monoamine Oxidase B Activity
Xueqiang Wu
1
,
Yifang Li
1
,
Jinhua Wang
1
,
Haibo Zhou
1
,
Xiao Tang
2
,
Ying Yang
3
,
Zhigang Wang
3
,
Dong Chen
4
,
Xia Zhou
1, 3
,
Jialiang Guo
1
,
Huaihong Cai
2
,
Junxia Zheng
5
,
Pinghua Sun
1
Publication type: Journal Article
Publication date: 2020-10-26
scimago Q1
wos Q1
SJR: 1.533
CiteScore: 11.6
Impact factor: 6.7
ISSN: 00032700, 15206882, 21542686
PubMed ID:
33103897
Analytical Chemistry
Abstract
Human monoamine oxidases (MAOs) play important roles in maintaining the homeostasis of biogenic amines. One of its isoforms, monoamine oxidase B (MAOB), is thought to be involved in several neurodegenerative diseases, which make the selective detection of MAOB activity essential. In this work, a novel surface-enhanced Raman scattering (SERS) sensor was fabricated and the MAOB activity was specifically determined by detecting the SERS signals of an enzyme-catalyzed reaction product via an amine-aldehyde click reaction. This process was simply achieved by coating core-shell gold-silver nanoparticles (Au@Ag NPs) on 3-aminopropyl aminopropyl triethoxysilane (APTES)-modified glass, and then, a monolayer of cysteamine (CA) was attached to the nanoparticle surface as a linker through Ag-S bonds. Using phenethylamine (PA) as a specific substrate of MAOB, the enzyme product phenylacetaldehyde (PAA) will produce significant Raman signals via the amine-aldehyde click reaction with CA, while other molecules, such as MAOB and PA, have no signal output because they cannot form close interaction with nanoparticles due to the existence of a CA layer. This sensor was further used for the specific determination of MAOB activity in clinical blood samples and the MAOB inhibitor assessment successfully. Meanwhile, by changing the click reaction types and taking advantage of the SERS fingerprint peaks for the specific click reaction products, this strategy offers huge potential to detect multiple enzyme activities simultaneously and can be used for new click reaction screening, enzyme-related disease diagnosis, drug screening, and clinical diagnosis.
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Total citations:
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Citations from 2024:
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(39.13%)
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GOST
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Wu X. et al. Click-Reaction-Triggered SERS Signals for Specific Detection of Monoamine Oxidase B Activity // Analytical Chemistry. 2020. Vol. 92. No. 22. pp. 15050-15058.
GOST all authors (up to 50)
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Wu X., Li Y., Wang J., Zhou H., Tang X., Yang Y., Wang Z., Chen D., Zhou X., Guo J., Cai H., Zheng J., Sun P. Click-Reaction-Triggered SERS Signals for Specific Detection of Monoamine Oxidase B Activity // Analytical Chemistry. 2020. Vol. 92. No. 22. pp. 15050-15058.
Cite this
RIS
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TY - JOUR
DO - 10.1021/acs.analchem.0c03017
UR - https://doi.org/10.1021/acs.analchem.0c03017
TI - Click-Reaction-Triggered SERS Signals for Specific Detection of Monoamine Oxidase B Activity
T2 - Analytical Chemistry
AU - Wu, Xueqiang
AU - Li, Yifang
AU - Wang, Jinhua
AU - Zhou, Haibo
AU - Tang, Xiao
AU - Yang, Ying
AU - Wang, Zhigang
AU - Chen, Dong
AU - Zhou, Xia
AU - Guo, Jialiang
AU - Cai, Huaihong
AU - Zheng, Junxia
AU - Sun, Pinghua
PY - 2020
DA - 2020/10/26
PB - American Chemical Society (ACS)
SP - 15050-15058
IS - 22
VL - 92
PMID - 33103897
SN - 0003-2700
SN - 1520-6882
SN - 2154-2686
ER -
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BibTex (up to 50 authors)
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@article{2020_Wu,
author = {Xueqiang Wu and Yifang Li and Jinhua Wang and Haibo Zhou and Xiao Tang and Ying Yang and Zhigang Wang and Dong Chen and Xia Zhou and Jialiang Guo and Huaihong Cai and Junxia Zheng and Pinghua Sun},
title = {Click-Reaction-Triggered SERS Signals for Specific Detection of Monoamine Oxidase B Activity},
journal = {Analytical Chemistry},
year = {2020},
volume = {92},
publisher = {American Chemical Society (ACS)},
month = {oct},
url = {https://doi.org/10.1021/acs.analchem.0c03017},
number = {22},
pages = {15050--15058},
doi = {10.1021/acs.analchem.0c03017}
}
Cite this
MLA
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Wu, Xueqiang, et al. “Click-Reaction-Triggered SERS Signals for Specific Detection of Monoamine Oxidase B Activity.” Analytical Chemistry, vol. 92, no. 22, Oct. 2020, pp. 15050-15058. https://doi.org/10.1021/acs.analchem.0c03017.