High-fidelity tracking of glycogen dynamics in living biosystems is critical for exploring the biological role of glycogen metabolism in diseases. However, information on the glycogen state mainly relies on a glucose uptake fluorescence probe 2-NBDG, which has proven to be extremely limited owing to the "always-on" fluorescence, short emission wavelength, and low signal-to-noise (S/N) ratio. Herein, we for the first time demonstrate a metabolic-activated off-on probe for glycogen through covalently attaching a molecular rotor with hydrophilic glucose at the C-2 position to guarantee good miscibility with a complete fluorescence-off state before metabolic incorporation into glycogen particles. The probe Glycogen-Red achieves negligible background fluorescence (1/30 times than 2-NBDG) and an ultrahigh S/N ratio (61-fold than 2-NBDG) of lighting-up near-infrared (NIR) fluorescence in glycogen biosynthesis. Notably, our probe has the unique characteristic of bypassing the washing steps, offering a powerful toolbox for real-time tracking of glycogen biosynthesis and super-resolution mapping of glycogen structures in living cells.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acssensors.5c00135 | DOI Listing |
Diabetes Metab J
March 2025
Department of Endocrinology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Sci Adv
March 2025
Functional Neuroimaging Laboratory, Istituto Italiano di Tecnologia, Center for Neuroscience and Cognitive Systems @UniTn, Rovereto, Italy.
Chromosome 22q11.2 deletion increases the risk of neuropsychiatric disorders like autism and schizophrenia. Disruption of large-scale functional connectivity in 22q11 deletion syndrome (22q11DS) has been widely reported, but the biological factors driving these changes remain unclear.
View Article and Find Full Text PDFSci Adv
March 2025
Clinical and Experimental Endocrinology, Department of Chronic Diseases and Metabolism, KU Leuven, Leuven, Belgium.
Carbohydrate-responsive element binding protein (ChREBP) and Max-like protein X (MLX) form a heterodimeric transcription factor complex that couples intracellular sugar levels to carbohydrate and lipid metabolism. To promote the expression of target genes, two ChREBP-MLX heterodimers form a heterotetramer to bind a tandem element with two adjacent E-boxes, called carbohydrate-responsive element (ChoRE). How the ChREBP-MLX hetero-tetramerization is achieved and regulated remains poorly understood.
View Article and Find Full Text PDFCells
February 2025
Department of Biological Sciences, Herbert H. Lehman College, City University of New York, 250 Bedford Park Boulevard West, New York, NY 10468, USA.
Interleukin 24 (IL-24) is a tumor-suppressing protein currently in clinical trials. We previously demonstrated that IL-24 leads to apoptosis in cancer cells through protein kinase A (PKA) activation in human breast cancer cells. To better understand the mechanism by which IL-24 induces apoptosis, we analyzed the role of glycogen synthase kinase-3 beta (GSK3β), a highly conserved serine/threonine kinase in cancer cells and a downstream target of PKA.
View Article and Find Full Text PDFFront Aging Neurosci
February 2025
Hospital of Encephalopathy, The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China.
Alzheimer's disease (AD) is a severe neurodegenerative disease characterized mainly by the formation of amyloid beta (Aβ) plaques and abnormal phosphorylation of tau. In recent years, an imbalance in iron homeostasis has been recognized to play a key role in the pathological process of AD. Abnormal iron accumulation can activate various kinases such as glycogen synthase kinase-3β, cyclin-dependent kinase 5, and mitogen-activated protein kinase, leading to abnormal phosphorylation of tau and amyloid precursor protein, and accelerating the formation of Aβ plaques and neurofibrillary tangles.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!