Evidence map›Paper›PMID 41867604›Full record

ArticleACS omega2026

Magneto-Photonic Gene Circuit for Minimally Invasive Control of Gene Expression in Mammalian Cells.

Enrique Alejandro Castellanos Franco, Ryan Radawiec, Ashley Slaviero, Connor J Grady, Brianna Ricker, Galit Pelled, Ute Hochgeschwender, Taeho Kim, Assaf A Gilad

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

5 · Who and what money

Authors and funding

9 authors.

Enrique Alejandro Castellanos FrancoDepartment of Biomedical Engineering, Michigan State University, East Lansing, Michigan 48824-1312, United States.ORCID https://orcid.org/0009-0007-6063-1102
Ryan RadawiecDepartment of Mechanical Engineering, Michigan State University, East Lansing, Michigan 48824-1312, United States.
Ashley SlavieroCollege of Medicine, Central Michigan University, Mount Pleasant, Michigan 48859, United States.
Connor J GradyDepartment of Biomedical Engineering, Michigan State University, East Lansing, Michigan 48824-1312, United States.
Brianna RickerDepartment of Chemical Engineering and Materials Science, Michigan State University, East Lansing, Michigan 48824-1312, United States.ORCID https://orcid.org/0000-0003-2216-9475
Galit PelledDepartment of Mechanical Engineering, Michigan State University, East Lansing, Michigan 48824-1312, United States.
Ute HochgeschwenderCollege of Medicine, Central Michigan University, Mount Pleasant, Michigan 48859, United States.
Taeho KimDepartment of Biomedical Engineering, Michigan State University, East Lansing, Michigan 48824-1312, United States.
Assaf A GiladDepartment of Chemical Engineering and Materials Science, Michigan State University, East Lansing, Michigan 48824-1312, United States.ORCID https://orcid.org/0000-0002-7272-7570

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precise control of gene expression is one of the fundamental goals of synthetic biology. Whether the objective is to modify endogenous cellular function or induce the expression of molecules for diagnostic and therapeutic purposes, gene regulation remains a key aspect of biological systems. Over time, advances in protein engineering and molecular biology have led to the creation of gene circuits capable of inducing the expression of specific proteins in response to external stimulus such as light. These optogenetic, or light-activated circuits hold significant potential for gene therapy as a tool for regulating the expression of therapeutic genes within cells. However, the applications of optogenetic systems can be limited by the lack of efficient ways to deliver light into cells or tissue. Our approach to address this challenge is to harness the power of bioluminescence to produce light directly inside cells using a luminescent enzyme. Combined with a photosensitive transcription factor, we report the development of a genetically encoded optogenetic circuit for the control of gene expression. Furthermore, we utilized a magneto-sensitive protein to engineer a split-protein version of this luminescent enzyme, where its reconstitution is driven by a 50 mT magnetic stimulus. Thus, resulting in a gene circuit activated by a combination of light and magnetic stimulus. We expect this work to advance the implementation of light-controlled systems without the need of external light sources, as well as serve as a basis for the development of future magneto-sensitive tools.

Identifiers

PMID41867604
PMCPMC13000775

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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.