State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing 210023, China.
Nano Lett. 2023 Apr 12;23(7):2800-2807. doi: 10.1021/acs.nanolett.3c00086. Epub 2023 Mar 16.
Obtaining sequential and conformational information on proteins is vital to understand their functions. Although the nanopore-based electrical detection can sense single molecule (SM) protein and distinguish among different amino acids, this approach still faces difficulties in slowing down protein translocation and improving ionic current signal-to-noise ratio. Here, we observe the unfolding and multistep sequential translocation of SM cytochrome c (cyt c) through a surface enhanced Raman scattering (SERS) active conical gold nanopore. High bias voltage unfolds SM protein causing more exposure of amino acid residues to the nanopore, which slows down the protein translocation. Specific SERS traces of different SM cyt c segments are then recorded sequentially when they pass through the hotspot inside the gold nanopore. This study shows that the combination of SM SERS with a nanopore can provide a direct insight into protein segments and expedite the development of nanopore toward SM protein sequencing.
获取蛋白质的序列和构象信息对于理解其功能至关重要。尽管基于纳米孔的电检测可以感知单分子(SM)蛋白质并区分不同的氨基酸,但这种方法在减缓蛋白质迁移和提高离子电流信噪比方面仍然面临困难。在这里,我们通过表面增强拉曼散射(SERS)活性锥形金纳米孔观察到 SM 细胞色素 c(cyt c)的展开和多步顺序迁移。高偏置电压使 SM 蛋白质展开,导致更多的氨基酸残基暴露于纳米孔中,从而减缓蛋白质迁移。当不同的 SM cyt c 片段通过金纳米孔内的热点时,会依次记录下特定的 SERS 痕迹。这项研究表明,SM SERS 与纳米孔的结合可以为蛋白质片段提供直接的洞察力,并加速纳米孔向 SM 蛋白质测序的发展。