A Self-Immolative Fluorescent Probe for Selective Detection of SARS-CoV-2 Main Protease.
Ming XuJiajing ZhouYong ChengZhicheng JinAlex E ClarkTengyu HeWonjun YimYi LiYu-Ci ChangZhuohong WuPavla FajtováAnthony J O'DonoghueAaron F CarlinMichael D ToddJesse V JokerstPublished in: Analytical chemistry (2022)
Existing tools to detect and visualize severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) suffer from low selectivity, poor cell permeability, and high cytotoxicity. Here we report a novel self-immolative fluorescent probe (MP590) for the highly selective and sensitive detection of the SARS-CoV-2 main protease (M pro ). This fluorescent probe was prepared by connecting a M pro -cleavable peptide ( N -acetyl-Abu-Tle-Leu-Gln) with a fluorophore ( i . e ., resorufin) via a self-immolative aromatic linker. Fluorescent titration results show that MP590 can detect M pro with a limit of detection (LoD) of 35 nM and is selective over interferents such as hemoglobin, bovine serum albumin (BSA), thrombin, amylase, SARS-CoV-2 papain-like protease (PL pro ), and trypsin. The cell imaging data indicate that this probe can report M pro in HEK 293T cells transfected with a M pro expression plasmid as well as in TMPRSS2-VeroE6 cells infected with SARS-CoV-2. Our results suggest that MP590 can both measure and monitor M pro activity and quantitatively evaluate M pro inhibition in infected cells, making it an important tool for diagnostic and therapeutic research on SARS-CoV-2.
Keyphrases
- sars cov
- fluorescent probe
- living cells
- respiratory syndrome coronavirus
- anti inflammatory
- sensitive detection
- high resolution
- single cell
- escherichia coli
- cell therapy
- single molecule
- cell cycle arrest
- coronavirus disease
- machine learning
- loop mediated isothermal amplification
- poor prognosis
- signaling pathway
- label free
- photodynamic therapy
- deep learning
- cell proliferation
- crispr cas
- endothelial cells
- big data
- artificial intelligence