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Sensitive assay of Human immunodeficiency virus (HIV) is the premise of accurate prevention and con-trol of AIDS. Dumbbell DNA showed promising potential in biosensing, imaging applications. This study presents a highly sensitive biosensing platform integrating dumbbell-shaped DNA probes with rolling circle transcription (RCT)-regulated CRISPR-Cas12a to achieve cascade signal amplification. The arrangement of the functional regions in the same unclosed dumbbell probes (UDPs) might affect final performance in the biosensor. Three different types UDPs (A/B/C) were specifically designed and the performances of the UDPs were evaluated in the RCT-CRISPR based cascade platform. Among these, type A UDP shows the best performance with a detection limit of 44.8 aM targeting HIV-DNA as well as high sensitivity and specificity. Also, type A UDP had the best behavior in the clinical sample assay. The difference of UDPs' performance might attribute to the variation of opening form of the UDPs considering the arrangement of various functional regions. The platform's modular design supports customization for diverse nucleic acid targets, making it adaptable for early disease detection and precision diagnostics.
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http://dx.doi.org/10.1016/j.aca.2025.344141 | DOI Listing |
Front Microbiol
August 2025
Ningbo Institute of Life and Health Industry, University of Chinese Academy of Sciences, Ningbo, Zhejiang, China.
Introduction: () is a well-known widespread food-borne pathogen that poses a threat to public health. Suitable detection methods are needed to effectively control and prevent pathogenic infections.
Methods: This study aimed to develop a novel closed dumbbell-mediated isothermal amplification (CDA)-based assay to achieve rapid and simple detection of The newly developed CDA technology is capable of amplifying DNA targets with high sensitivity and specificity.
Plant Signal Behav
September 2025
I-Cultiver, Inc., Manteca, CA, USA.
Francis Darwin (1848-1925) was one of the first to study in detail the development and function of stomata. However, since the green leaves of flowering plants are the most conspicuous and suitable organs for the study of cell development and transpiration activity, most of this "Darwinian" research has focused on these sun-exposed organs. In this study, we analyzed the development of stomata along the hypocotyl of 5-day-old light-grown sunflower () seedlings.
View Article and Find Full Text PDFBiosens Bioelectron
December 2025
School of Chemistry and Chemical Engineering, State Key Laboratory of Digital Medical Engineering, Southeast University, Nanjing, 211189, China. Electronic address:
β: β-Glucosyltransferase (β-GT) is a pivotal enzymatic tool for 5-hydroxymethylcytosine (5-hmC) detection, and it can specifically catalyze the glycosylation of 5-hmC. This enzymatic reaction plays a crucial role in modulating bacteriophage-specific gene expression and facilitating the survival of bacteriophages and parasites within host cells. Herein, we engineer a multi-modular and structurally ordered CRISPR/Cas-based biomachine by integrating 5-hmC glycosylation-triggered palindrome-primed hyperbranched rolling circle amplification (PP-HRCA) for ultrasensitive analysis of exogenous β-GT activity.
View Article and Find Full Text PDFTalanta
July 2025
Hubei Key Laboratory of Pollutant Analysis & Reuse Technology, College of Chemistry and Chemical Engineering, Hubei Normal University, Huangshi, 435002, Hubei, China. Electronic address:
Flap endonuclease 1 (FEN1), a structure-specific nuclease, is usually overexpressed in various types of cancer cells and has been recognized as a promising biomarker for molecular diagnostics. In this work, we developed a one-tube and ultrasensitive method for FEN1 sensing based on customized target recognition, exponential signal amplification and nano-signal transduction. Due to rational palindrome design, only two DNA substrates and a pair of enzymes were needed in the sensing.
View Article and Find Full Text PDFJ Hazard Mater
September 2025
Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China. Electronic address:
Herein, we developed a photoelectrochemical (PEC) biosensor integrating SrTiO and SnO materials with a dumbbell DNA mediated target recycling system to quantify microRNA-21 levels under bisphenol A (BPA) exposure. The engineered SrTiO/SnO photoelectrode demonstrated enhanced charge separation efficiency due to band alignment, yielding a remarkable 33-fold photocurrent enhancement compared to that of pure SrTiO. In addition, a dumbbell DNA-based signal amplification strategy was designed and the target microRNA-21 was converted to DNA nanospheres, which can "switch-on" the PEC signal by loading the signal mediator methylene blue.
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