Molecular Pharmacology Program, Sloan Kettering Institute, New York, New York 10065, United States.
School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
J Am Chem Soc. 2024 May 8;146(18):12454-12462. doi: 10.1021/jacs.4c00149. Epub 2024 Apr 30.
Quantum defects in single-walled carbon nanotubes promote exciton localization, which enables potential applications in biodevices and quantum light sources. However, the effects of local electric fields on the emissive energy states of quantum defects and how they can be controlled are unexplored. Here, we investigate quantum defect sensitization by engineering an intrinsically disordered protein to undergo a phase change at a quantum defect site. We designed a supercharged single-chain antibody fragment (scFv) to enable a full ligand-induced folding transition from an intrinsically disordered state to a compact folded state in the presence of a cytokine. The supercharged scFv was conjugated to a quantum defect to induce a substantial local electric change upon ligand binding. Employing the detection of a proinflammatory biomarker, interleukin-6, as a representative model system, supercharged scFv-coupled quantum defects exhibited robust fluorescence wavelength shifts concomitant with the protein folding transition. Quantum chemical simulations suggest that the quantum defects amplify the optical response to the localization of charges produced upon the antigen-induced folding of the proteins, which is difficult to achieve in unmodified nanotubes. These findings portend new approaches to modulate quantum defect emission for biomarker sensing and protein biophysics and to engineer proteins to modulate binding signal transduction.
单壁碳纳米管中的量子缺陷促进激子局域化,这使其在生物器件和量子光源中有潜在的应用。然而,局部电场对量子缺陷发射能态的影响以及如何控制这些影响尚未得到探索。在这里,我们通过设计一种内在无序的蛋白质在量子缺陷位点发生相变来研究量子缺陷敏化。我们设计了一种带正电荷的单链抗体片段(scFv),使其在细胞因子存在的情况下,能够从无序状态完全诱导折叠转变。带正电荷的 scFv 与量子缺陷结合,在配体结合时会引起局部电场的显著变化。我们使用促炎生物标志物白细胞介素 6 的检测作为代表性模型系统,带正电荷的 scFv 偶联的量子缺陷在蛋白质折叠转变时表现出强烈的荧光波长移动。量子化学模拟表明,量子缺陷放大了对配体诱导蛋白质折叠时产生的电荷局域化的光学响应,这在未经修饰的纳米管中很难实现。这些发现预示着新的方法可以调节量子缺陷发射,用于生物标志物传感和蛋白质生物物理学,以及设计蛋白质来调节结合信号转导。