1,709 research outputs found

    On-chip light-scattering enhancement enables high performance single-particle tracking under conventional bright-field microscope

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    Scattering-based single-particle tracking (S-SPT) has opened new avenues for highly sensitive label-free detection and characterization of nanoscopic objects, making it particularly attractive for various analytical applications. However, a long-standing issue hindering its widespread applicability is its high technical demands on optical systems. The most promising solution entails implementing on-chip light-scattering enhancement, but the existing field-enhancement technology fails as their highly localized field is insufficient to cover the three-dimensional trajectory of particles within the interrogation time. Here, we present a straightforward and robust on-chip microlens-based strategy for light-scattering enhancement, providing an enhancement range ten times greater than that of near-field optical techniques. These properties are attributed to the increased long-range optical fields and complex composite interactions between two closely spaced structures. Thanks to this strategy, we demonstrate that high-performance S-SPT can be achieved, for the first time, under a conventional bright-field microscope with illumination powers over 1,000 times lower than typically required. This significantly reduces the technical demands of S-SPT, representing a significant step forward in facilitating its practical application in biophotonics, biosensors, diagnostics, and other fields.Comment: 29 pages,4 figure

    Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation

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    OBJECTIVE: The aim of this study was to evaluate the prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation (AF). METHODS: A cohort of 136 unrelated patients with idiopathic atrial fibrillation and 200 unrelated, ethnically matched healthy controls were enrolled. The coding exons and splice junctions of the Nkx2.5 gene were sequenced in 136 atrial fibrillation patients, and the available relatives of mutation carriers and 200 controls were subsequently genotyped for the identified mutations. The functional characteristics of the mutated Nkx2.5 gene were analyzed using a dual-luciferase reporter assay system. RESULTS: Two novel heterozygous Nkx2.5 mutations (p.N19D and p.F186S) were identified in 2 of the 136 unrelated atrial fibrillation cases, with a mutational prevalence of approximately 1.47%. These missense mutations co-segregated with atrial fibrillation in the families and were absent in the 400 control chromosomes. Notably, 2 mutation carriers also had congenital atrial septal defects and atrioventricular block. Multiple alignments of the Nkx2.5 protein sequences across various species revealed that the altered amino acids were completely conserved evolutionarily. Functional analysis demonstrated that the mutant Nkx2.5 proteins were associated with significantly reduced transcriptional activity compared to their wild-type counterpart. CONCLUSION: These findings associate the Nkx2.5 loss-of-function mutation with atrial fibrillation and atrioventricular block and provide novel insights into the molecular mechanism involved in the pathogenesis of atrial fibrillation. These results also have potential implications for early prophylaxis and allele-specific therapy of this common arrhythmia
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