Evidence map›Paper›PMID 42495361›Full record

ArticleACS omega2026

Theoretical Design of All-Optical Universal Logic via Multistage FRET-STED Energy Cascades in Fluorescent Protein Nanoclusters.

Balázs Rakos

Abstract read
In one paragraph

Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Balázs RakosDepartment of Automation and Applied Informatics, Budapest University of Technology and Economics, Budapest H-1117, Hungary.ORCID https://orcid.org/0000-0002-9148-8771

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The scaling limits of conventional electronics necessitate a shift toward alternative physical computing substrates. We present a universal logic design based on a novel materials platform employing FRET-coupled Fluorescent Protein (FP) NOR gates. By leveraging the nonlinear dynamics of Stimulated Emission Depletion (STED) to bypass slow protein backbone rearrangements, this system enables all-optical switching at speeds ranging from 1 GHz to potentially even 1 THz. We developed a dynamic multistage model of a three-protein FRET-STED cascade to evaluate performance. While a "lifetime bottleneck" initially limits standard operation, we demonstrate that engineering the plasmonic environment via Nanometal Surface Energy Transfer (NSET) enables 1 GHz operation with current protein variants. Analysis of fundamental electronic transitionsspecifically vibrational relaxationconfirms a theoretical bandwidth of ∼3.15 THz for optimized synthetic chromoproteins. This work establishes a robust foundation for high-speed, nanoscale, all-optical computing using DNA origami as a molecular breadboard for precise sub-10 nm positioning.

Identifiers

PMID42495361
PMCPMC13392890

What OpenQuestion holds

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Registered trials

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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.