Quantum spin resonance in engineered proteins for multimodal sensing
Sensing technologies that exploit quantum phenomena for measurement are finding increasing applications across materials, physical and biological sciences<sup>1-7</sup>. Until recently, biological candidates for quantum sensors were limited to in vitro systems, had poor sensitivity and were prone to light-induced degradation. These limitations impeded practical biotechnological applications, and high-throughput study that would facilitate their engineering and optimization. We recently developed a class of magneto-sensitive fluorescent proteins including MagLOV, which overcomes many of these challenges<sup>8</sup>. Here we show that through directed evolution, it is possible to engineer these proteins to alter the properties of their response to magnetic fields and radio frequencies. We find that MagLOV exhibits optically detected magnetic resonance in living bacterial cells at room temperature, at sufficiently high signal-to-noise for single-cell detection. These effects are explained through the radical-pair mechanism, which involves the protein backbone and a bound flavin cofactor. Using optically detected magnetic resonance and fluorescence magnetic-field effects, we explore a range of applications, including spatial localization of fluorescence signals using gradient fields (that is, magnetic resonance imaging using a genetically encoded probe), sensing of the molecular microenvironment, multiplexing of bio-imaging and lock-in detection, mitigating typical biological imaging challenges such as light scattering and autofluorescence. Taken together, our results represent a suite of sensing modalities for engineered biological systems, based on and designed around understanding the quantum-mechanical properties of magneto-sensitive fluorescent proteins.
Authors
- Scott Stacey
- Jack J. Miller (ORCID: https://orcid.org/0000-0002-6258-1299)
- Harrison Steel (ORCID: https://orcid.org/0000-0002-9625-4755)
- Jean‐Philippe Tetienne (ORCID: https://orcid.org/0000-0001-5796-2508)
- Maria Ingaramo (ORCID: https://orcid.org/0000-0003-4244-696X)
- Idris Kempf (ORCID: https://orcid.org/0000-0002-9304-2773)
- Gabriel Abrahams (ORCID: https://orcid.org/0000-0002-2360-7150)
- Andrew G. York
- Lewis Antill
- Robin Henry
- Andrew G. York
- Vincent Spreng
- Kirill Sechkar
- Jessica James
- Vicente Trelles-Fernandez
- Ana Štuhec
Institutions
- Aarhus University (DK)
- Heidelberg University (DE)
- University of Oxford (GB)
- Enzo Life Sciences (United States) (US)
- Science Oxford (GB)
- RMIT University (AU)
- Sungkyunkwan University (KR)
Publication Details
- Journal
- Nature
- Published
- 2026-01-21
- DOI
- https://doi.org/10.1038/s41586-025-09971-3
- Citations
- 8
- Primary Topic
- bioluminescence and chemiluminescence research
- Type
- article
- Field-Weighted Citation Impact
- 177.90
Funders
- UK Research and Innovation
- Leverhulme Trust
- European Commission
- Novo Nordisk Fonden
- Directorate for Biological Sciences
- Engineering and Physical Sciences Research Council
- Biotechnology and Biological Sciences Research Council