tetano
Editor, Senior Moderator
Anal Chem
. 2021 Nov 3.
doi: 10.1021/acs.analchem.1c03807. Online ahead of print.
Construction of Optimal SERS Hotspots Based on Capturing the Spike Receptor-Binding Domain (RBD) of SARS-CoV-2 for Highly Sensitive and Specific Detection by a Fish Model
Guangyao Huang[SUP] 1 2 3 [/SUP], Hongxin Zhao[SUP] 4 [/SUP], Pan Li[SUP] 1 [/SUP], Juanjuan Liu[SUP] 4 [/SUP], Siyu Chen[SUP] 1 2 [/SUP], Meihong Ge[SUP] 1 2 [/SUP], Miao Qin[SUP] 1 2 [/SUP], Guoliang Zhou[SUP] 1 2 [/SUP], Yongtao Wang[SUP] 1 2 [/SUP], Shaofei Li[SUP] 1 2 [/SUP], Yizhuang Cheng[SUP] 1 2 [/SUP], Qiang Huang[SUP] 5 [/SUP], Junfeng Wang[SUP] 4 [/SUP], Hongzhi Wang[SUP] 1 2 3 [/SUP], Liangbao Yang[SUP] 1 2 3 [/SUP]
Affiliations
Abstract
It is highly challenging to construct the best SERS hotspots for the detection of proteins by surface-enhanced Raman spectroscopy (SERS). Using its own characteristics to construct hotspots can achieve the effect of sensitivity and specificity. In this study, we built a fishing mode device to detect the receptor-binding domain (RBD) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) at low concentrations in different detection environments and obtained a sensitive SERS signal response. Based on the spatial resolution of proteins and their protein-specific recognition functions, SERS hotspots were constructed using aptamers and small molecules that can specifically bind to RBD and cooperate with Au nanoparticles (NPs) to detect RBD in the environment using SERS signals of beacon molecules. Therefore, two kinds of AuNPs modified with aptamers and small molecules were used in the fishing mode device, which can specifically recognize and bind RBD to form a stable hotspot to achieve high sensitivity and specificity for RBD detection. The fishing mode device can detect the presence of RBD at concentrations as low as 0.625 ng/mL and can produce a good SERS signal response within 15 min. Meanwhile, we can detect an RBD of 0.625 ng/mL in the mixed solution with various proteins, and the concentration of RBD in the complex environment of urine and blood can be as low as 1.25 ng/mL. This provides a research basis for SERS in practical applications for protein detection work.
. 2021 Nov 3.
doi: 10.1021/acs.analchem.1c03807. Online ahead of print.
Construction of Optimal SERS Hotspots Based on Capturing the Spike Receptor-Binding Domain (RBD) of SARS-CoV-2 for Highly Sensitive and Specific Detection by a Fish Model
Guangyao Huang[SUP] 1 2 3 [/SUP], Hongxin Zhao[SUP] 4 [/SUP], Pan Li[SUP] 1 [/SUP], Juanjuan Liu[SUP] 4 [/SUP], Siyu Chen[SUP] 1 2 [/SUP], Meihong Ge[SUP] 1 2 [/SUP], Miao Qin[SUP] 1 2 [/SUP], Guoliang Zhou[SUP] 1 2 [/SUP], Yongtao Wang[SUP] 1 2 [/SUP], Shaofei Li[SUP] 1 2 [/SUP], Yizhuang Cheng[SUP] 1 2 [/SUP], Qiang Huang[SUP] 5 [/SUP], Junfeng Wang[SUP] 4 [/SUP], Hongzhi Wang[SUP] 1 2 3 [/SUP], Liangbao Yang[SUP] 1 2 3 [/SUP]
Affiliations
- PMID: 34730332
- DOI: 10.1021/acs.analchem.1c03807
Abstract
It is highly challenging to construct the best SERS hotspots for the detection of proteins by surface-enhanced Raman spectroscopy (SERS). Using its own characteristics to construct hotspots can achieve the effect of sensitivity and specificity. In this study, we built a fishing mode device to detect the receptor-binding domain (RBD) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) at low concentrations in different detection environments and obtained a sensitive SERS signal response. Based on the spatial resolution of proteins and their protein-specific recognition functions, SERS hotspots were constructed using aptamers and small molecules that can specifically bind to RBD and cooperate with Au nanoparticles (NPs) to detect RBD in the environment using SERS signals of beacon molecules. Therefore, two kinds of AuNPs modified with aptamers and small molecules were used in the fishing mode device, which can specifically recognize and bind RBD to form a stable hotspot to achieve high sensitivity and specificity for RBD detection. The fishing mode device can detect the presence of RBD at concentrations as low as 0.625 ng/mL and can produce a good SERS signal response within 15 min. Meanwhile, we can detect an RBD of 0.625 ng/mL in the mixed solution with various proteins, and the concentration of RBD in the complex environment of urine and blood can be as low as 1.25 ng/mL. This provides a research basis for SERS in practical applications for protein detection work.