SARS-CoV-2 Receptor Binding Domain as a Stable-Potential Target for SARS-CoV-2 Detection by Surface-Enhanced Raman Spectroscopy

被引:20
作者
Awada, Chawki [1 ]
Abdullah, Mohammed Mahfoudh B. A. [2 ]
Traboulsi, Hassan [3 ]
Dab, Chahinez [4 ]
Alshoaibi, Adil [1 ]
机构
[1] King Faisal Univ, Dept Phys, Coll Sci, POB 400, Al Hasa 31982, Saudi Arabia
[2] King Faisal Univ, Dept Biol Sci, Coll Sci, POB 400, Al Hasa 31982, Saudi Arabia
[3] King Faisal Univ, Dept Chem, Coll Sci, POB 400, Al Hasa 31982, Saudi Arabia
[4] Univ Montreal, Dept Chim, Campus MIL, Montreal, PQ H2V 0B3, Canada
关键词
SERS; SARS-COV-2 receptor binding domain; silver; gold nanostructures; BSA; PROTEINS; SERS;
D O I
10.3390/s21134617
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, we report a new approach for detecting SARS-CoV-2 RBD protein (RBD) using the surface-enhanced Raman spectroscopy (SERS) technique. The optical enhancement was obtained thanks to the preparation of nanostructured Ag/Au substrates. Fabricated Au/Ag nanostructures were used in the SERS experiment for RBD protein detection. SERS substrates show higher capabilities and sensitivity to detect RBD protein in a short time (3 s) and with very low power. We were able to push the detection limit of proteins to a single protein detection level of 1 pM. The latter is equivalent to 1 fM as a detection limit of viruses. Additionally, we have shown that the SERS technique was useful to figure out the presence of RBD protein on antibody functionalized substrates. In this case, the SERS detection was based on protein-antibody recognition, which led to shifts in the Raman peaks and allowed signal discrimination between RBD and other targets such as Bovine serum albumin (BSA) protein. A perfect agreement between a 3D simulated model based on finite element method and experiment was reported confirming the SERS frequency shift potential for trace proteins detection. Our results could open the way to develop a new prototype based on SERS sensitivity and selectivity for rapid detection at a very low concentration of virus and even at a single protein level.
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页数:16
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