Fluorogenic Peptide Sensor Array Derived from Angiotensin-Converting Enzyme 2 Classifies Severe Acute Respiratory Syndrome Coronavirus 2 Variants of Concern.
Wei-Tao DouPei-Hong TongMan XingJiao-Jiao LiuXi-Le HuTony David JamesDong-Ming ZhouXiao-Peng HePublished in: Journal of the American Chemical Society (2024)
The devastating COVID-19 pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has made society acutely aware of the urgency in developing effective techniques to timely monitor the outbreak of previously unknown viral species as well as their mutants, which could be even more lethal and/or contagious. Here, we report a fluorogenic sensor array consisting of peptides truncated from the binding domain of human angiotensin-converting enzyme 2 (hACE2) for SARS-CoV-2. A set of five fluorescently tagged peptides were used to construct the senor array in the presence of different low-dimensional quenching materials. When orthogonally incubated with the wild-type SARS-CoV-2 and its variants of concern (VOCs), the fluorescence of each peptide probe was specifically recovered, and the different recovery rates provide a "fingerprint" characteristic of each viral strain. This, in turn, allows them to be differentiated from each other using principal component analysis. Interestingly, the classification result from our sensor array agrees well with the evolutionary relationship similarity of the VOCs. This study offers insight into the development of effective sensing tools for highly contagious viruses and their mutants based on rationally truncating peptide ligands from human receptors.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- angiotensin converting enzyme
- wild type
- angiotensin ii
- high throughput
- endothelial cells
- high resolution
- high density
- copy number
- induced pluripotent stem cells
- living cells
- pluripotent stem cells
- coronavirus disease
- machine learning
- deep learning
- genome wide
- fluorescent probe
- energy transfer
- gene expression
- quantum dots
- mass spectrometry
- single molecule
- transcription factor
- genetic diversity
- sensitive detection
- dna binding
- binding protein