ArticleNature communications2025
Raman identification of single nucleotides flowing through permeable plasmonic films.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Stress-induced ripping enables fabrication of nanopores with dimensions smaller than the resolution limit of the employed lithography.Science advances · 2026Article
- Single-Molecule Peptide Discrimination via Flow-Through SERS and Machine Learning.ACS photonics · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
16 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Surface-Enhanced Raman Scattering has been studied for decades as a recognition technique due to its high sensitivity and discriminative power, particularly in biological applications. Inspired by nanopore sequencing technology, we developed a plasmonic device capable of operating in a flow-through configuration to detect individual molecules passing through plasmonic hotspots. This device is a permeable plasmonic film, through which single molecules are sequentially delivered via electrophoresis, while Raman spectra are recorded in real-time. A very effective light-matter coupling, combined with the ultrasmall size of plasmonic spots, enabled access to angstrom spatial and microsecond temporal scales compatible with polymer sequencing. We successfully slowed the translocation process and captured Raman spectra of the four nucleotides at a time resolution down to 20 μs under our experimental conditions. We achieved a discrimination accuracy of 89% at the single-molecule level. Also, we demonstrated a spatial resolution on the order of a few nucleotides, suggesting the potential for sequencing applications.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.