指纹(计算)
生物系统
维数之咒
拉曼散射
电子鼻
拉曼光谱
表面增强拉曼光谱
分析物
材料科学
计算机科学
纳米技术
模式识别(心理学)
人工智能
化学
物理
光学
色谱法
生物
作者
Nayoung Kim,Michael R. Thomas,Mads S. Bergholt,Isaac J. Pence,Hyejeong Seong,Patrick Charchar,Nevena Todorova,Anika Nagelkerke,Alexis Belessiotis‐Richards,David J. Payne,Amy Gelmi,Irene Yarovsky,Molly M. Stevens
标识
DOI:10.1038/s41467-019-13615-2
摘要
Abstract Label-free surface-enhanced Raman spectroscopy (SERS) can interrogate systems by directly fingerprinting their components’ unique physicochemical properties. In complex biological systems however, this can yield highly overlapping spectra that hinder sample identification. Here, we present an artificial-nose inspired SERS fingerprinting approach where spectral data is obtained as a function of sensor surface chemical functionality. Supported by molecular dynamics modeling, we show that mildly selective self-assembled monolayers can influence the strength and configuration in which analytes interact with plasmonic surfaces, diversifying the resulting SERS fingerprints. Since each sensor generates a modulated signature, the implicit value of increasing the dimensionality of datasets is shown using cell lysates for all possible combinations of up to 9 fingerprints. Reliable improvements in mean discriminatory accuracy towards 100% are achieved with each additional surface functionality. This arrayed label-free platform illustrates the wide-ranging potential of high-dimensionality artificial-nose based sensing systems for more reliable assessment of complex biological matrices.
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