Evidence map›Paper›PMID 39833147›Full record

ArticleNature communications2025

Fluorescein-based SynNotch adaptors for regulating gene expression responses to diverse extracellular and matrix-based cues.

Jeremy C Tran, Christopher J Kuffner, Alexander M Marzilli, Ryan Emily Miller, Zachary E Silfen, Jeffrey B McMahan, D Christopher Sloas, Christopher S Chen, John T Ngo

Abstract read
In one paragraph

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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jeremy C TranDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.ORCID http://orcid.org/0000-0001-6692-5899
Christopher J KuffnerDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.ORCID http://orcid.org/0000-0002-4379-677X
Alexander M MarzilliDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.ORCID http://orcid.org/0000-0002-8173-8941
Ryan Emily MillerDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Zachary E SilfenDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.ORCID http://orcid.org/0009-0002-1175-7327
Jeffrey B McMahanDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.ORCID http://orcid.org/0000-0001-5845-605X
D Christopher SloasDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Christopher S ChenDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.ORCID http://orcid.org/0000-0003-2445-8449
John T NgoDepartment of Biomedical Engineering, Boston University, Boston, MA, USA. jtngo@bu.edu.ORCID http://orcid.org/0000-0003-3508-1915

Funding

TRAINING PROGRAM IN QUANTITATIVE BIOLOGY AND PHYSIOLOGYT32GM008764 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI WHITE, JOHN A. · 2001 to 2021
$5.9M
Integrative Approaches for Probing Cell Mechanotransduction in Health and DiseaseR35GM128859 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI John Tuan Ngo · 2018 to 2026
$3.3M
Notch signaling and adhesion regulationR01HL147585 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI CHEN, CHRISTOPHER S · 2019 to 2022
$1.6M
NHLBI NIH HHS R01 HL147585NIGMS NIH HHS R35 GM128859NIGMS NIH HHS T32 GM008764U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01HL147585U.S. Department of Health & Human Services | National Institutes of Health (NIH) R35GM128859U.S. Department of Health & Human Services | National Institutes of Health (NIH) T32GM008764
6 · The paper itself

Abstract

Synthetic Notch (SynNotch) receptors function like natural Notch proteins and can be used to install customized sense-and-respond capabilities into mammalian cells. Here, we introduce an adaptor-based strategy for regulating SynNotch activity via fluorescein isomers and analogs. Using an optimized fluorescein-binding SynNotch receptor, we describe ways to chemically control SynNotch signaling, including an approach based on a bio-orthogonal chemical ligation and a spatially controllable strategy via the photo-patterned uncaging of an o-nitrobenzyl-caged fluorescein conjugate. We further show that fluorescein-conjugated extracellular matrix (ECM)-binding peptides can be used to regulate SynNotch activity depending on the folding state of collagen-based ECM networks. To demonstrate the utility of these tools, we apply them to activate dose-dependent gene expression responses and to induce myogenic-like phenotypes in multipotent fibroblasts with spatiotemporal and microenvironmental control. Overall, we introduce an optimized fluorescein-binding SynNotch as a versatile tool for regulating transcriptional responses to ligands based on the clinically-approved fluorescein dye.

Indexed as

Extracellular MatrixFluoresceinGene Expression RegulationReceptors, NotchAnimalsFibroblastsHumansMiceSignal TransductionFluoresceinReceptors, Notch

Identifiers

PMID39833147
PMCPMC11756391

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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.