Protease-Responsive Potential-Tunable AIEgens for Cell Selective Imaging of TMPRSS2 and Accurate Inhibitor Screening.
Yong ChengAlex E ClarkWonjun YimRaina M BorumYu-Ci ChangZhicheng JinTengyu HeAaron F CarlinJesse V JokerstPublished in: Analytical chemistry (2023)
Transmembrane protease serine 2 (TMPRSS2) is a plasma membrane protease that activates both spike protein of coronaviruses for cell entry and oncogenic signaling pathways for tumor progression. TMPRSS2 inhibition can reduce cancer invasion and metastasis and partially prevent the entry of SARS-CoV-2 into host cells. Thus, there is an urgent need for both TMPRSS2-selective imaging and precise screening of TMPRSS2 inhibitors. Here, we report a TMPRSS2-responsive surface-potential-tunable peptide-conjugated probe (EGTP) with aggregation-induced emission (AIE) features for TMPRSS2 selective imaging and accurate inhibitor screening. The amphiphilic EGTP was constructed with tunable surface potential and responsive efficiency with TMPRSS2 and its inhibitor. The rational construction of AIE luminogens (AIEgens) with modular peptides indicated that the cleavage of EGTP led to a gradual aggregation with bright fluorescence in high TMPRSS2-expressing cells. This strategy may have value for selective detection of cancer cells, SARS-CoV-2-target cells, and screening of protease inhibitors.
Keyphrases
- sars cov
- induced apoptosis
- high resolution
- cell cycle arrest
- signaling pathway
- cancer therapy
- endoplasmic reticulum stress
- living cells
- cell therapy
- respiratory syndrome coronavirus
- cell death
- stem cells
- quantum dots
- drug delivery
- squamous cell carcinoma
- poor prognosis
- human health
- small molecule
- young adults
- light emitting
- protein protein
- high density