Turn-on Rhodamine Glycoconjugates Enable Real-Time GLUT Activity Monitoring in Live Cells and In Vivo.
Monica Mame Soma NyansaAdelina OronovaNazar GoraMicaela Rayne GeborkoffNathan Randal OstlundDelaney Raine FritzThomas WernerMarina TanasovaPublished in: Chemical & biomedical imaging (2023)
The direct relationship between facilitative glucose transporters (GLUTs) and metabolic diseases opens new avenues for sensing metabolic deregulations and drives the development of molecular probes for GLUT-targeted detection of metabolic diseases. Radiotracer-based molecular imaging probes have been effectively utilized in reporting alterations in sugar uptake as an indication of metabolic deregulations, cancer development, or inflammation. Progress in developing fluorophore-based tools facilitated GLUT-specific analyses using more accessible fluorescence-based instrumentation. However, restrictions on the emission range of fluorophores and the requirement for substantial post-treatments to reduce background fluorescence have brought to light the critical directions for improvement of the technology for broader use in screening applications. Here we present turn-on GLUT activity reporters activated upon cells' internalization. We demonstrate a specific delivery of a sizable rhodamine B fluorophore through GLUT5 and showcase a stringent requirement in conjugate structure for maintaining a GLUT-specific uptake. With the turn-on GLUT probes, we demonstrate the feasibility of high-throughput fluorescence microscopy and flow cytometry-based GLUT activity screening in live cells and the probes' applicability for assessing sugar uptake alterations in vivo .
Keyphrases
- fluorescent probe
- living cells
- single molecule
- induced apoptosis
- high throughput
- cell cycle arrest
- small molecule
- flow cytometry
- sensitive detection
- cell death
- computed tomography
- signaling pathway
- blood pressure
- cancer therapy
- blood glucose
- skeletal muscle
- papillary thyroid
- pet imaging
- type diabetes
- optical coherence tomography
- drug delivery
- cell proliferation
- high speed
- pi k akt
- positron emission tomography
- photodynamic therapy
- glycemic control
- drug induced