Institute of Chemistry, University of Potsdam, Potsdam 14469, Germany.
Nano Lett. 2024 Jun 12;24(23):6916-6923. doi: 10.1021/acs.nanolett.4c00834. Epub 2024 Jun 3.
Cytochrome C, an evolutionarily conserved protein, plays pivotal roles in cellular respiration and apoptosis. Understanding its molecular intricacies is essential for both academic inquiry and potential biomedical applications. This study introduces an advanced single-molecule surface-enhanced Raman scattering (SM-SERS) system based on DNA origami nanoantennas (DONAs), optimized to provide unparalleled insights into protein structure and interactions. Our system effectively detects shifts in the Amide III band, thereby elucidating protein dynamics and conformational changes. Additionally, the system permits concurrent observations of oxidation processes and Amide bands, offering an integrated view of protein structural and chemical modifications. Notably, our approach diverges from traditional SM-SERS techniques by de-emphasizing resonance conditions for SERS excitation, aiming to mitigate challenges like peak oversaturation. Our findings underscore the capability of our DONAs to illuminate single-molecule behaviors, even within aggregate systems, providing clarity on molecular interactions and behaviors.
细胞色素 C 是一种进化上保守的蛋白质,在细胞呼吸和细胞凋亡中发挥关键作用。了解其分子复杂性对于学术研究和潜在的生物医学应用都至关重要。本研究介绍了一种先进的基于 DNA 折纸纳米天线 (DONAs) 的单分子表面增强拉曼散射 (SM-SERS) 系统,该系统经过优化,可提供对蛋白质结构和相互作用的无与伦比的深入了解。我们的系统能够有效地检测到酰胺 III 带的移动,从而阐明蛋白质的动力学和构象变化。此外,该系统还可以同时观察氧化过程和酰胺带,提供蛋白质结构和化学修饰的综合视图。值得注意的是,我们的方法通过降低 SERS 激发的共振条件来淡化传统的 SM-SERS 技术,旨在减轻峰过饱和等挑战。我们的研究结果强调了 DONAs 阐明单分子行为的能力,即使在聚集体系中也是如此,为分子相互作用和行为提供了清晰的认识。