Fluorogenic Peptide Sensor Array Derived from Angiotensin-Converting Enzyme 2 Classifies Severe Acute Respiratory Syndrome Coronavirus 2 Variants of Concern.

J Am Chem Soc

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, 130 Meilong Rd., Shanghai 200237, China.

Published: July 2024

AI Article Synopsis

  • The COVID-19 pandemic highlighted the need for better methods to monitor and identify new and mutated viruses, such as SARS-CoV-2.
  • Researchers developed a fluorogenic sensor array using fluorescently tagged peptides from the hACE2 binding domain, designed to detect different strains of the virus.
  • The sensor array effectively distinguished between wild-type SARS-CoV-2 and its variants through unique fluorescence patterns, correlating with their evolutionary relationships, thus aiding in the rapid identification of viral strains.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11295173PMC
http://dx.doi.org/10.1021/jacs.4c06172DOI Listing

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