J Phys Chem Lett. 2021 Apr 1;12(12):3187-3194. doi: 10.1021/acs.jpclett.1c00240. Epub 2021 Mar 24.
Surface-enhanced Raman scattering (SERS) circumvents the inherent insensitivity of Raman spectroscopy and offers a powerful tool for the ultrasensitive detection and characterization of biomolecules at low concentrations. Here we show that SERS via electrostatic tethering between surface-modified negatively charged silver nanoparticles and highly positively charged intrinsically disordered N-terminal domain of the prion protein allows highly sensitive and reproducible protein detection and characterization at as low as hundreds of nanomolar protein concentrations. These measurements preferentially illuminate a selective part of the protein due to a sharp dependence of the near-field intensity on the distance between the nanoparticle surface and the protein. We also demonstrate that by shortening the length of the disordered tail it is possible to achieve a domain-selective Raman enhancement to study the C-terminal globular domain. Our tether-length-dependent SERS methodology will serve as a potent, noninvasive, and label-free strategy to detect and characterize a wide range of proteins possessing disordered segments.
表面增强拉曼散射(SERS)克服了拉曼光谱固有的不灵敏性,为在低浓度下对生物分子进行超灵敏检测和特征分析提供了有力工具。在这里,我们展示了通过表面修饰的带负电荷的银纳米粒子与朊病毒蛋白的高度正电荷的无规卷曲的 N 端结构域之间的静电束缚作用产生的 SERS,可在低至数百纳摩尔的蛋白浓度下实现高度灵敏和可重现的蛋白检测和特征分析。这些测量由于近场强度与纳米粒子表面和蛋白质之间的距离的强烈依赖性,优先照亮蛋白质的选择性部分。我们还证明,通过缩短无规尾的长度,可以实现对 C 端球状结构域的选择性 Raman 增强,以研究该结构域。我们的基于束缚长度的 SERS 方法将成为一种强大的、非侵入性的、无标记的策略,用于检测和分析具有无规片段的广泛的蛋白质。