Tanwar Swati, Zheng Peng, Wu Lintong, Barman Ishan
Department of Mechanical Engineering, Johns Hopkins University, Baltimore, MD 21218, USA.
The Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University, School of Medicine, Baltimore, MD 21205, USA; Department of Oncology, Johns Hopkins University, Baltimore, MD 21287, USA.
Biosens Bioelectron. 2025 Oct 15;286:117615. doi: 10.1016/j.bios.2025.117615. Epub 2025 May 21.
Early detection is essential for improving cancer treatment outcomes. Surface-enhanced Raman scattering (SERS) offers high sensitivity and molecular specificity but suffers from slow imaging speed when used independently. Here, we introduce stimuli-responsive bimodal SERS-dark-field (DF) nanoprobes for rapid and selective imaging of metastatic prostate cancer cells. These nanoprobes utilize legumain enzyme-responsive peptide coatings on plasmonic gold nanocubes and a bio-orthogonal self-condensation mechanism to facilitate enzyme-triggered nanoprobe aggregation. Upon internalization, the nanoprobes selectively aggregate in DU145 cells that overexpress legumain, while remaining uniformly dispersed in LNCaP cells with minimal legumain activity. DF microscopy quickly identifies these aggregates, significantly expediting subsequent SERS imaging. The engineered design of these nanoprobes ensures distinct vibrational signatures specifically correlated to enzyme activity, establishing a direct link between enzymatic presence and SERS signal generation. By combining the rapid localization capabilities of DF imaging with the molecular precision of SERS, our bimodal imaging strategy significantly surpasses conventional single-modal SERS techniques, providing a versatile platform for fast and accurate detection of various diseases through their distinctive enzymatic profiles.
早期检测对于改善癌症治疗结果至关重要。表面增强拉曼散射(SERS)具有高灵敏度和分子特异性,但单独使用时成像速度较慢。在此,我们引入了刺激响应型双峰SERS-暗场(DF)纳米探针,用于转移性前列腺癌细胞的快速和选择性成像。这些纳米探针利用等离子体金纳米立方体上的legumain酶响应肽涂层和生物正交自缩合机制来促进酶触发的纳米探针聚集。内化后,纳米探针在过表达legumain的DU145细胞中选择性聚集,而在具有最小legumain活性的LNCaP细胞中保持均匀分散。DF显微镜可快速识别这些聚集体,显著加快后续的SERS成像。这些纳米探针的工程设计确保了与酶活性特异性相关的独特振动特征,在酶的存在与SERS信号产生之间建立了直接联系。通过将DF成像的快速定位能力与SERS的分子精度相结合,我们的双峰成像策略显著超越了传统的单峰SERS技术,为通过其独特的酶谱快速准确地检测各种疾病提供了一个通用平台。