Evidence map›Paper›PMID 41112935›Full record

ArticleAnalytical science advances2025

Evaluation of the Ligand-Independent Activation of a VHH-Based Anti-CD19 SynNotch Receptor by Dual-Luciferase Assay.

Yasaman Asaadi, Fatemeh Rahbarizadeh

Abstract read
In one paragraph

Article in Analytical science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. Article
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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

2 authors.

Yasaman AsaadiDepartment of Biotechnology College of Science University of Tehran Tehran Iran.ORCID https://orcid.org/0000-0002-8223-6054
Fatemeh RahbarizadehDepartment of Medical Biotechnology Faculty of Medical Sciences Tarbiat Modares University Tehran Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ligand-independent activation poses a significant challenge for synthetic receptors, limiting their dynamic range. Given the difficulties and inconsistencies in evaluating this crucial aspect in many studies, we utilized a dual-luciferase assay to assess the background activity of the SynNotch receptor. These receptors are modular, orthogonal constructs designed to detect and respond to specific extracellular signals by expressing a targeted protein. In this study, we engineered an anti-CD19 SynNotch receptor by incorporating a nanobody into the antigen-binding domain, leveraging the advantageous properties of camelid VHHs. We then evaluated the performance of the final construct, focusing on its functionality and ligand-independent activation using the dual-luciferase assay. The results revealed that although reporter expression significantly increased in the presence of the antigen, there was also a high level of background expression, which could hinder the performance of the SynNotch receptor. Additionally, the SynNotch receptor exhibited a 24-h delay in reaching its peak activation level in response to the antigen and in returning to baseline levels in its absence. Therefore, the optimization of the SynNotch construct is essential to enhance the receptor's dynamic range.

Indexed as

dual‐luciferase assay | ligand independent activation | nanobody | SynNotch receptor | synthetic receptor

Identifiers

PMID41112935
PMCPMC12533965

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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.