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Related Concept Videos

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Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
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Fluorometers and spectrofluorometers are two types of instruments used for measuring molecular fluorescence. These instruments differ in how they select excitation and emission wavelengths and the type of light sources they utilize. Fluorometers use absorption interference filters to choose excitation and emission wavelengths. The excitation source in a fluorometer is typically a low-pressure mercury vapor lamp that emits intense lines distributed throughout the ultraviolet and visible regions.
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Updated: Sep 10, 2025

Effect of Fluorescent Proteins on Fusion Partners Using Polyglutamine Toxicity Assays in Yeast
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A fluorescent-protein spin qubit.

Jacob S Feder1, Benjamin S Soloway1, Shreya Verma2

  • 1Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL, USA.

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|August 20, 2025
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Summary
This summary is machine-generated.

Researchers developed a new quantum bit (qubit) using enhanced yellow fluorescent protein. This biological qubit allows for optical control and readout, demonstrating potential for nanoscale sensing in living cells.

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Area of Science:

  • Quantum Information Science
  • Biophysics
  • Molecular Biology

Background:

  • Optically addressable spin qubits are crucial for nanoscale sensing, primarily engineered in solid-state systems.
  • Fluorescent proteins are widely used in vivo microscopy due to genetic encodability, but their potential as qubits remains unexplored.
  • Fluorescent proteins possess a metastable triplet state, a key characteristic for qubit functionality.

Purpose of the Study:

  • To engineer and characterize an optically addressable spin qubit within a fluorescent protein.
  • To investigate the feasibility of using fluorescent proteins as a platform for quantum information processing.
  • To demonstrate the functionality of these biological qubits in complex biological environments.

Main Methods:

  • Realization of an optically addressable spin qubit in enhanced yellow fluorescent protein.
  • Utilizing near-infrared laser pulses for triggered readout of the triplet state.
  • Employing coherent microwave control and Carr-Purcell-Meiboom-Gill decoupling for coherence time measurements at liquid-nitrogen temperatures.
  • Expressing the qubit in mammalian and bacterial cells to assess performance in vivo.

Main Results:

  • Achieved triggered readout of the enhanced yellow fluorescent protein spin qubit with up to 20% spin contrast.
  • Measured a coherence time of (16 ± 2) μs at liquid-nitrogen temperatures.
  • Demonstrated sustained qubit contrast and coherent control within mammalian cells.
  • Observed optically detected magnetic resonance in bacterial cells at room temperature with up to 8% contrast.

Conclusions:

  • Fluorescent proteins represent a novel and powerful platform for creating optical spin qubits.
  • This biological qubit technology opens avenues for life science applications, including nanoscale sensing and spin-based imaging.
  • The ability to engineer qubits within genetically encoded fluorescent proteins offers significant advantages for in vivo quantum applications.