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Quantum Defect Sensitization via Phase-Changing Supercharged Antibody Fragments.
Mijin Kim1,2, James J McCann3, Jacob Fortner4,5
1Molecular Pharmacology Program, Sloan Kettering Institute, New York, New York 10065, United States.
Journal of the American Chemical Society
|April 30, 2024
Summary
We engineered proteins on quantum defects in carbon nanotubes to detect biomarkers. This method creates a detectable fluorescence shift upon protein folding, enabling new biosensing applications.
Area of Science:
- Quantum Information Science
- Biophysics
- Materials Science
Background:
- Quantum defects in single-walled carbon nanotubes (SWCNTs) are crucial for exciton localization, with potential in biodevices and quantum light sources.
- The influence of local electric fields on quantum defect emission and control mechanisms remain largely unexplored.
Purpose of the Study:
- To investigate quantum defect sensitization by engineering a protein to undergo a phase change at a quantum defect site.
- To develop a method for controlling quantum defect emission using protein conformational changes for biomarker detection.
Main Methods:
- Designed a supercharged single-chain antibody fragment (scFv) for ligand-induced folding.
- Conjugated the supercharged scFv to SWCNT quantum defects.
- Utilized interleukin-6 (IL-6) as a model proinflammatory biomarker.
- Performed quantum chemical simulations to understand the underlying mechanisms.
Main Results:
- Supercharged scFv-coupled quantum defects showed significant fluorescence wavelength shifts upon IL-6 binding and protein folding.
- The protein folding transition induced a substantial local electric field change at the quantum defect site.
- Quantum chemical simulations indicated amplified optical responses due to charge localization during protein folding.
Conclusions:
- Engineered proteins can effectively modulate quantum defect emission in SWCNTs.
- This approach enables sensitive biomarker detection and offers new strategies for protein biophysics studies.
- The findings pave the way for engineering proteins to control binding signal transduction in nanomaterials.
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