A ratiometric fluorescent sensor for rapid detection of the pyroglutamate aminopeptidase-1 in mouse tumors.
Ting CaoLiang ZhangLei ZhengJing QianAnam IqbalKanwal IqbalWenwu QinYun LiuPublished in: Journal of materials chemistry. B (2021)
Pyroglutamate aminopeptidase-1 (PGP-1) is an important enzyme that plays an indispensable role in the process of inflammation. Up to now, few reports have been reported on the detection of PGP-1 activity in vivo and in vitro, and there are no reports on ratiometric detection. Here, the first red-emitting ratiometric fluorescent sensor (DP-1) for the specific detection of PGP-1 both in vivo and in vitro was designed and synthesized by using DCD-NH2 as the luminescent parent and pyroglutamate as a recognition group. After interacting with PGP-1, the amide bond is hydrolyzed by the enzyme and the color of the solution changes from yellow (λabs = 420 nm) to red (λabs = 520 nm), accompanied by obvious fluorescence emission wavelength change (from ∼564 nm to ∼616 nm). The probe has high specificity and sensitivity towards PGP-1 in about 10 min, and the DL is as low as 0.25 ng mL-1. Interestingly, under the stimulation of Freund's incomplete adjuvant and lipopolysaccharide, the imaging of DP-1 in HepG2 and RAW264 cells shows that the expression of PGP-1 is associated with inflammation. What's more, for the first, the imaging of a mouse tumor model confirms that the enzyme is closely related to the occurrence of some inflammation and tumor diseases. These results indicate that DP-1 can be used as an effective tool for real-time monitoring of PGP-1 levels both in vivo and in vitro and the study of inflammatory tumor pathology.
Keyphrases
- quantum dots
- living cells
- fluorescent probe
- oxidative stress
- sensitive detection
- energy transfer
- photodynamic therapy
- label free
- loop mediated isothermal amplification
- high resolution
- single molecule
- early stage
- induced apoptosis
- risk assessment
- real time pcr
- hydrogen peroxide
- fluorescence imaging
- emergency department
- adverse drug
- long non coding rna
- cell death
- cell proliferation
- room temperature
- endoplasmic reticulum stress
- electronic health record
- oxide nanoparticles