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DNA molecular switches have emerged as a versatile and highly programmable toolbox and are extensively used in sensing, diagnosis, and therapeutics. Toehold mediated strand displacement serves as the core reaction for signal transduction and amplification. However, the severe leakage of this reaction limits the development of scalable and robust circuits. We engineered single-molecule dynamic DNA junctions for developing 'zero-leakage' molecular switches which are responsive to various inputs. Input binding enhances dynamic junctions' stability allowing for the transient binding of fluorescent probes as the output signal. Unlike the conventional intensity-based output, this molecular switch provides remarkably distinguishable kinetics-based outputs permitting ruling out leakage signals at the single-molecule level. The inputs are detected with significant sensitivity without using any amplification step. It is also revealed that the output signal is sensitive to the binding affinity of inputs and their recognition elements making the molecular switch a potential affinity meter. Considering these features, we anticipate that it would find broad applications in large-scale DNA circuits, responsive materials, and biomolecule interaction study.
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http://dx.doi.org/10.1039/c9sc03389k | DOI Listing |
Org Lett
September 2025
College of Chemistry and Chemical Engineering, Key Laboratory of Hunan Province for Chemical Power Source, Central South University, Changsha 410083, China.
We designed a molecular switch based on a cavitand and pyrene. The controllable switching properties of the cavitand paired with flexible chains are some of the best combinations for achieving robustness in complex environments. A rigid chain cavitand was also synthesized as a control, and its single crystals with high molecular weights were obtained.
View Article and Find Full Text PDFNeuropsychiatr Dis Treat
August 2025
Department of Psychiatry and Behavioral Sciences, New York Medical College, Valhalla, New York, USA.
Brexpiprazole is a second-generation antipsychotic with multiple indications, including the treatment of schizophrenia. As a partial dopamine agonist, brexpiprazole differs from most other antipsychotics, yet uncertainties about its full mechanism of action have led to some ambiguity among prescribers. To address this gap, an international panel of psychiatric experts was organized and convened with funding from Otsuka Pharmaceutical Europe Ltd and H.
View Article and Find Full Text PDFFront Mol Neurosci
August 2025
Zhuhai Maternal and Child Health Care Hospital, (Guangxi University of Chinese Medicine), Zhuhai, China.
[This corrects the article DOI: 10.3389/fnmol.2025.
View Article and Find Full Text PDFChem Sci
September 2025
Tianjin Key Laboratory of Micro-scale Optical Information Science and Technology, Institute of Modern Optics and Centre of Single-Molecule Science, Nankai University Tianjin 300350 China
The keto-enol tautomerism, involving a reversible isomerization of the molecule, plays a critical role in organic synthesis, biological activity, and molecular-scale charge transport. It is therefore essential to manipulate the process of keto-enol tautomerism. Unlike typical ketones, β-diketones exist dominantly in the enol form and it is a great challenge to realize enol-keto tautomerism due to the formation of intramolecular hydrogen bonds in the enol form.
View Article and Find Full Text PDFiScience
September 2025
Department of Physiology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Fibroblasts can be transformed into myofibroblasts under pro-fibrotic conditions, which are characterized by increased contractility and reduced matrix degradation. The relationship between contractile activity and matrix degradation is not fully understood. To mimic physiological conditions, fibroblasts were cultured on a collagen gel with low rigidity.
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