Back to Search Start Over

A paper-based optical sensor for the screening of viruses through the cysteine residues of their surface proteins: A proof of concept on the detection of coronavirus infection.

Authors :
Gholami, Mahnaz D.
Guppy-Coles, Kristyan
Nihal, Serena
Langguth, Daman
Sonar, Prashant
Ayoko, Godwin A.
Punyadeera, Chamindie
Izake, Emad L.
Source :
Talanta. Oct2022, Vol. 248, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a serious threat to human health. Current methods such as reverse transcription polymerase chain reaction (qRT-PCR) are complex, expensive, and time-consuming. Rapid, and simple screening methods for the detection of SARS-CoV-2 are critically required to fight the current pandemic. In this work we present a proof of concept for, a simple optical sensing method for the screening of SARS-CoV-2 through its spike protein subunit S1. The method utilizes a target-specific extractor chip to bind the protein from the biological specimens. The disulfide bonds of the protein are then reduced into a biothiol with sulfhydryl (SH) groups that react with a blue-colored benzothiazole azo dye-Hg complex (BAN-Hg) and causes the spontaneous change of its blue color to pink which is observable by the naked eye. A linear relationship between the intensity of the pink color and the logarithm of reduced S1 protein concentration was found within the working range 130 ng.mL−1-1.3 pg mL−1. The lowest limit of detection (LOD) of the assay was 130 fg mL−1. A paper based optical sensor was fabricated by loading the BAN-Hg sensor onto filter paper and used to screen the S1 protein in spiked saliva and patients' nasopharyngeal swabs. The results obtained by the paper sensor corroborated with those obtained by qRT-PCR. The new paper-based sensing method can be extended to the screening of many viruses (e.g. the human immunodeficiency virus, the human polyomavirus, the human papilloma virus, the adeno associated viruses, the enteroviruses) through the cysteine residues of their capsid proteins. The new method has strong potential for screening viruses at pathology labs and in remote areas that lacks advanced scientific infrastructure. Further clinical studies are warranted to validate the new sensing method. [Display omitted] • A proof of concept on an optical sensor for screening viruses through the capsid proteins. • The sensor was used to detect SARS-CoV-2 through the S1 protein. • The free cysteine of the protein causes the sensor color to change spontaneously. • The sensor detected the protein in biological specimens down to 130 fg mL−1 • The sensing method is rapid when compared to qRT-PCR. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00399140
Volume :
248
Database :
Academic Search Index
Journal :
Talanta
Publication Type :
Academic Journal
Accession number :
157418691
Full Text :
https://doi.org/10.1016/j.talanta.2022.123630