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.
Authors
- Wenxin Hu (ORCID: https://orcid.org/0000-0001-9957-0078)
- Mark J. Zylka (ORCID: https://orcid.org/0000-0003-0911-7902)
- Sophia U Lamberti (ORCID: https://orcid.org/0009-0005-2147-6686)
- Lei Xing (ORCID: https://orcid.org/0000-0003-2646-018X)
- Trinity E Rust
- Hannah C. Nourie
Institutions
- University of North Carolina at Chapel Hill (US)
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