A luminescence-based biosensor to measure endogenous UBE3A activity

Loss- and gain-of-function (LOF and GOF) mutations in the E3 ubiquitin ligase UBE3A cause distinct neurodevelopmental disorders. The AZUL domain of UBE3A binds with low nanomolar affinity to a 45 amino acid (aa) region of PSMD4. We fused this 45-aa sequence to Firefly luciferase to generate a luminescence-based biosensor, Firefly-45aa, that acts as an artificial UBE3A substrate and exhibits exceptional sensitivity in measuring UBE3A activity. Testing UBE3A variants using Firefly-45aa in HEK293T cells revealed distinct biosensor activity profiles, enabling the classification of LOF and GOF mutations based on maximum activity, inhibitory concentration-50, and activity per unit of protein. Some strong LOF mutations had dominant negative activity. In addition, Firefly-45aa can be used to quantify endogenous UBE3A activity in primary cells from Angelman syndrome and GOF mouse models. This biosensor reveals a mutational spectrum of UBE3A enzyme activity and is a sensitive tool for functional characterization and therapeutic development in UBE3A-related disorders.

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Publication Details

Journal
iScience
Published
2025-10-04
DOI
https://doi.org/10.1016/j.isci.2025.113684
Citations
1
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
1.82
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article

A luminescence-based biosensor to measure endogenous UBE3A activity

Wenxin Hu, Mark J. Zylka, Sophia U Lamberti, Lei Xing et al.
1 citations
iScience
Genetics and Neurodevelopmental Disorders
1.82
article

A luminescence-based biosensor to measure endogenous UBE3A activity

Wenxin Hu, Mark J. Zylka, Sophia U Lamberti, Lei Xing, Trinity E Rust, Hannah C. Nourie
article en
1 citations

Abstract

Loss- and gain-of-function (LOF and GOF) mutations in the E3 ubiquitin ligase UBE3A cause distinct neurodevelopmental disorders. The AZUL domain of UBE3A binds with low nanomolar affinity to a 45 amino acid (aa) region of PSMD4. We fused this 45-aa sequence to Firefly luciferase to generate a luminescence-based biosensor, Firefly-45aa, that acts as an artificial UBE3A substrate and exhibits exceptional sensitivity in measuring UBE3A activity. Testing UBE3A variants using Firefly-45aa in HEK293T cells revealed distinct biosensor activity profiles, enabling the classification of LOF and GOF mutations based on maximum activity, inhibitory concentration-50, and activity per unit of protein. Some strong LOF mutations had dominant negative activity. In addition, Firefly-45aa can be used to quantify endogenous UBE3A activity in primary cells from Angelman syndrome and GOF mouse models. This biosensor reveals a mutational spectrum of UBE3A enzyme activity and is a sensitive tool for functional characterization and therapeutic development in UBE3A-related disorders.

iScienceVol. 28(11)
University of North Carolina at Chapel Hill (US)
Openalex Percentile: Top 12%
Genetics and Neurodevelopmental Disorders
1.82
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A luminescence-based biosensor to measure endogenous UBE3A activity — Wenxin Hu, Mark J. Zylka, et al. · iScience (2025) | TGRS Research Map | TGRS