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A fluorescent-protein spin qubit

Author

Listed:
  • Jacob S. Feder

    (University of Chicago)

  • Benjamin S. Soloway

    (University of Chicago)

  • Shreya Verma

    (University of Chicago)

  • Zhi Z. Geng

    (University of Chicago)

  • Shihao Wang

    (University of Chicago)

  • Bethel B. Kifle

    (University of Chicago)

  • Emmeline G. Riendeau

    (University of Chicago)

  • Yeghishe Tsaturyan

    (University of Chicago)

  • Leah R. Weiss

    (University of Chicago)

  • Mouzhe Xie

    (University of Chicago
    Arizona State University)

  • Jun Huang

    (University of Chicago)

  • Aaron Esser-Kahn

    (University of Chicago
    LLC)

  • Laura Gagliardi

    (University of Chicago
    University of Chicago
    University of Chicago)

  • David D. Awschalom

    (University of Chicago
    University of Chicago
    Argonne National Laboratory)

  • Peter C. Maurer

    (University of Chicago
    LLC
    Argonne National Laboratory)

Abstract

Quantum bits (qubits) are two-level quantum systems that support initialization, readout and coherent control1. Optically addressable spin qubits form the foundation of an emerging generation of nanoscale sensors2–7. The engineering of these qubits has mainly focused on solid-state systems. However, fluorescent proteins, rather than exogenous fluorescent probes, have become the gold standard for in vivo microscopy because of their genetic encodability8,9. Although fluorescent proteins possess a metastable triplet state10, they have not been investigated as qubits. Here we realize an optically addressable spin qubit in enhanced yellow fluorescent protein. A near-infrared laser pulse enables triggered readout of the triplet state with up to 20% spin contrast. Using coherent microwave control of the enhanced-yellow-fluorescent-protein spin at liquid-nitrogen temperatures, we measure a (16 ± 2) μs coherence time under Carr–Purcell–Meiboom–Gill decoupling. We express the qubit in mammalian cells, maintaining contrast and coherent control despite the complex intracellular environment. Finally, we demonstrate optically detected magnetic resonance in bacterial cells at room temperature with contrast up to 8%. Our results introduce fluorescent proteins as a powerful qubit platform that paves the way for applications in the life sciences, such as nanoscale field sensing and spin-based imaging modalities.

Suggested Citation

  • Jacob S. Feder & Benjamin S. Soloway & Shreya Verma & Zhi Z. Geng & Shihao Wang & Bethel B. Kifle & Emmeline G. Riendeau & Yeghishe Tsaturyan & Leah R. Weiss & Mouzhe Xie & Jun Huang & Aaron Esser-Kah, 2025. "A fluorescent-protein spin qubit," Nature, Nature, vol. 645(8079), pages 73-79, September.
  • Handle: RePEc:nat:nature:v:645:y:2025:i:8079:d:10.1038_s41586-025-09417-w
    DOI: 10.1038/s41586-025-09417-w
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