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Autophagy is a ubiquitous process of organelle interaction in eukaryotic cells, in which various organelles or proteins are recycled and operated through the autophagy pathway to ensure nutrient and energy homeostasis. Although numerous fluorescent probes have been developed to image autophagy, these environment-responsive probes suffer from inherent deficiencies such as inaccuracy and limited versatility. Here, we present a modular macrocyclic amphiphile Förster Resonance Energy Transfer (FRET) platform (SC6A12C/NCM, SN), constructed through the amphiphilic assembly of sulfonatocalix[6]arene (SC6A12C) with N-cetylmorpholine (NCM) for lysosome targeting. The hydrophobic fluorophore BPEA (FRET donor) was entrapped within the inner hydrophobic phase and showed strong fluorescence emission. Attributed to the broad-spectrum encapsulation of SC6A12C, three commercially available organelle probes (Mito-Tracker Red, ER Tracker Red, and RhoNox-1) were selected as SC6A12C guests (FRET acceptors). During autophagy process, the formation of intracellular host-guest complexes leads to strong FRET signal, allowing us to visualize the fusion of mitochondria, endoplasmic reticulum, and Golgi apparatus with lysosomes, respectively. This study provides a versatile and accessible platform for imaging organelle autophagy.
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http://dx.doi.org/10.1002/anie.202420793 | DOI Listing |
Adv Sci (Weinh)
August 2025
School of Pharmacy, Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi, 563000, China.
The intricate pathological mechanisms of Alzheimer's disease (AD), along with the restrictive nature of the blood-brain barrier (BBB) that further impedes the drug brain entry, underscore the pressing need for innovative combinational therapy to achieve effective treatment outcomes. Intranasal administration, capable of bypassing BBB by direct transport through olfactory and trigeminal nerves, provides a promising approach for treating neurological disorders. Herein, the guanidinium-modified calix[5]arene (GC5AY) is developed as a single-molecule pleuripotent scaffold, demonstrating small size, positive charge and desirable amphiphilicity, which facilitate its efficient traverse of nasal mucosal barrier.
View Article and Find Full Text PDFPhys Chem Chem Phys
August 2025
Department of Chemistry, Center for Innovative Technology, Vanderbilt University, Nashville, TN 37235, USA.
Cyclodextrins (CDs) are macrocyclic oligosaccharides that have the ability to form host-guest inclusion complexes due to their amphiphilic properties, thereby allowing for an increase in the solubility and bioavailability of encapsulated small molecules, such as food constituents and active pharmaceutical ingredients (APIs). While solution-phase properties of CD inclusion complexes have been extensively studied, less is known about the prevailing coordination environment of metal-CD complexes in the absence of bulk solvent. Here, we investigate the gas-phase structural implications of alkali-metal complexation with the three naturally occurring cyclodextrins (αCD, βCD, and γCD) and a suite of linear maltodextrins using structurally-selective ion mobility-mass spectrometry (IM-MS) analysis.
View Article and Find Full Text PDFChemistryOpen
August 2025
CPCV, Department of Chemistry, Ecole Normale Supérieure, PSL University, Sorbonne Université, CNRS, 75005, Paris, France.
Pseudo-rotaxanes are reversibly interlocked molecules with at least one linear molecule threaded into a macrocycle and, contrary to rotaxanes, an advantageous ability to be dissociated. Cyclodextrins constitute attracting macrocyclic host entities to build such dynamic structures for their oligosaccharide nature, conic shape, amphiphilic character and biocompatibility. Here we show that using an azobenzene DNA intercalator as a guest allows to build a pseudo-rotaxane combining several remarkable properties, including light-controlled assembly/disassembly, photoreversible chirality and fluorescence, as well as the capability to affect the melting temperature of double-stranded DNA through intercalator host-guest complexation.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemistry, State Key Lab of Molecular Engineering of Polymers, and Shanghai Key Lab of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200438, China.
The stereochemistry of chiral macrocycles bearing multiple chirality has a crucial influence on their physical and biological properties. Nevertheless, the multiple chirality induction in macrocyclizations remains largely unexplored in the synthetic community. Here we report that confined macrocyclizations in single-layer chiral porous sheets can generate macrocyclic products bearing multiple chirality with excellent stereoselectivity.
View Article and Find Full Text PDFChemistry
September 2025
Analysis and Testing Center, Nantong University, No.9 Seyuan Road, Chongchuan District, Nantong, Jiangsu, 226019, P. R. China.
As a new generation of supramolecular host macrocyclic molecules, pillararenes display many advantages including simple synthesis routes, rigid electron-rich structures, unique host-guest interactions, and adjustable cavity sizes, which make them widely be used in drug delivery systems for precise diagnosis and treatment of cancer. The molecular functions of pillararenes can be easily expanded through the introduction of different functional groups into the side chain. For example, polyethylene glycol (PEG) which has good biocompatibility and water solubility can be used to construct PEG-functionalized amphiphilic pillararenes.
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