98%
921
2 minutes
20
Photoactivatable probes can switch fluorescence on from a weak or nonemission state to improve the sensitivity of the sensing system. In this work, we successfully constructed three highly emissive photoactivatable probes, 2-DP, 1-2-DP and 2-2-DP, for Cu detection. Under UV irradiation, the photoluminescence quantum yields of 2-DP, 1-2-DP and 2-2-DP display approximately 52.4-, 11.5- and 49.2-fold enhancement, respectively. Cu selectively quenches the bright photoactivated fluorescence, resulting in an approximately 38-fold fluorescence reduction. The highly selective fluorescence response to Cu yields an excellent low detection limit of 5.8 nM. Moreover, the photoactivatable probes were successfully applied for Cu determination in tap water and tea samples with recovery ranges of 95%-105% and 97%-106%, respectively. This work provides a more sensitive and efficient methodology for Cu detection in heavy metal pollution and food safety.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.foodchem.2023.137439 | DOI Listing |
bioRxiv
August 2025
Department of Physiology and Biophysics, University of Illinois Chicago, IL, USA.
Despite the success of endocrine therapy (ET) in treating hormone receptor-positive breast cancer, a significant proportion of patients relapse during or after treatment, making ET resistance a major clinical challenge. Previously we have shown that ET-resistant breast cancer cells exhibit reduced ceramide levels and an increased sensitivity to ceramide-induced cell death. Here, we demonstrate that ceramides induce a distinct transcriptional reprogramming in ET-resistant cells, characterized by upregulation of endoplasmic reticulum stress (EnRS) pathways.
View Article and Find Full Text PDFTalanta
August 2025
Key Laboratory of Biorheological Science and Technology, Ministry of Education, College of Bioengineering, Chongqing University, No. 174 Shazheng Road, Chongqing, 400044, PR China. Electronic address:
Electrochemical detection of microRNA biomarkers in tumor interstitial fluid is promising for accurately assessing tumor burden, but remains challenging due to interference and reproducibility limitations. Here, a magnetic separation-integrated electrochemical biosensor utilizing the synergy of photo-electronic cascading was developed for anti-interference and highly reproductive detection of miRNA-21. Polydopamine-coated FeO magnetic nanoparticles were adopted as electroactive probe carriers and photoactivatable electron donors.
View Article and Find Full Text PDFArXiv
July 2025
= Departments of Molecular Immunology and Immunology and Chemical Physiology and Biochemistry, Oregon Health & Science University, Portland, OR, USA.
Lipid-protein interactions play essential roles in cellular signaling and membrane dynamics, yet their systematic characterization has long been hindered by the inherent biochemical properties of lipids. Recent advances in functionalized lipid probes - equipped with photoactivatable crosslinkers, affinity handles, and photocleavable protecting groups - have enabled proteomics-based identification of lipid interacting proteins with unprecedented specificity and resolution. Despite the growing number of published lipid interactomes, there remains no centralized effort to harmonize, compare, or integrate these datasets.
View Article and Find Full Text PDFACS Sens
August 2025
Department of Chemistry, Texas A&M University, College Station, Texas 77843, United States.
Base excision repair (BER) is a biologically and biomedically important cellular pathway responsible for repairing common DNA lesions. As a central member of the BER pathway, apurinic/apyrimidinic endonuclease 1 (APE1) is important in DNA repair and has been identified as a diagnostic and predictive biomarker for several diseases, motivating the development of analytical methods. However, the current repertoire of APE1 probes, the majority of which are derived from nucleic acids, are poorly suited for use in living cells and organisms, putting many promising biomedical applications of APE1 out of reach.
View Article and Find Full Text PDFChem Sci
August 2025
Astbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds Leeds LS2 9JT UK
Photoreactive groups are invaluable tools in structural proteomics, offering reagent-free activation and temporal control of protein labelling. However, traditional UV-activatable functional groups often produce unstable intermediates and diverse products, making these chemistries difficult to deploy at scale. In this study, we performed a systematic analysis of -nitrobenzyl alcohol (NBA) reactivity for integration into novel reagents for chemical crosslinking-mass spectrometry.
View Article and Find Full Text PDF