Mid-infrared enhanced spectrochemical detection using azide vibrational probes.

IF 10.7 1区 生物学 Q1 BIOPHYSICS Biosensors and Bioelectronics Pub Date : 2025-03-15 Epub Date: 2024-12-19 DOI:10.1016/j.bios.2024.117083
Valentina Di Meo, Gennaro Sanità, Angela Oliver, Annamaria Sandomenico, Massimo Moccia, Ivo Rendina, Alessio Crescitelli, Vincenzo Galdi, Menotti Ruvo, Emanuela Esposito
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Abstract

Spectrochemical analysis of trace elements in complex matrices is crucial across various fields of science, industry, and technology. However, this analysis is often hindered by background interference and the challenge of detecting ultralow analyte concentrations. Surface Enhanced Infrared Absorption (SEIRA) spectroscopy is emerging as a viable technique to address these challenges as it can successfully reveal soluble and unmodified analytes in a label-free manner through their interactions with a bioreceptor following site-specific labeling with small infrared-active probes. In this study, we present and demonstrate an advanced method for mid-infrared spectroscopy utilizing a pixeled SEIRA substrate coupled with a peculiar infrared-active vibrational probe. We select a small azide moiety as the vibrational tag since its signature around 2100 cm-1 is in the cell- and protein-silent window and its small size preserves the structure and biological function of the protein it integrates into. As model bioreceptor, we utilize an antigen-binding fragment (Fab') derived from the therapeutic antibody trastuzumab, modified with azidoacetic acid, and its Her2 antigen as the soluble analyte. Employing mid-infrared SEIRA spectroscopy, we are able to monitor the immobilization of the azide-modified Fab', and demonstrate the detection of analyte quantities as low as 83 amol within an area of 100 μm2.

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叠氮化物振动探针的中红外增强光谱化学检测。
复杂基质中微量元素的光谱化学分析在科学、工业和技术的各个领域都是至关重要的。然而,这种分析经常受到背景干扰和检测超低分析物浓度的挑战的阻碍。表面增强红外吸收(SEIRA)光谱技术正在成为解决这些挑战的一种可行技术,因为它可以通过与生物受体的相互作用,通过小型红外活性探针进行位点特异性标记,以无标记的方式成功地揭示可溶性和未修饰的分析物。在这项研究中,我们提出并展示了一种先进的中红外光谱方法,利用像素化SEIRA衬底加上一种特殊的红外主动振动探针。我们选择了一个小叠氮化物片段作为振动标签,因为它在2100 cm-1左右的特征位于细胞和蛋白质沉默窗口,而且它的小尺寸保留了它所整合的蛋白质的结构和生物学功能。作为模型生物受体,我们使用了来自治疗性抗体曲妥珠单抗的抗原结合片段(Fab’),用叠氮乙酸修饰,其Her2抗原作为可溶性分析物。利用中红外SEIRA光谱,我们能够监测叠氮化物修饰的Fab'的固定化,并证明在100 μm2的面积内检测到低至83 amol的分析物。
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来源期刊
Biosensors and Bioelectronics
Biosensors and Bioelectronics 工程技术-电化学
CiteScore
20.80
自引率
7.10%
发文量
1006
审稿时长
29 days
期刊介绍: Biosensors & Bioelectronics, along with its open access companion journal Biosensors & Bioelectronics: X, is the leading international publication in the field of biosensors and bioelectronics. It covers research, design, development, and application of biosensors, which are analytical devices incorporating biological materials with physicochemical transducers. These devices, including sensors, DNA chips, electronic noses, and lab-on-a-chip, produce digital signals proportional to specific analytes. Examples include immunosensors and enzyme-based biosensors, applied in various fields such as medicine, environmental monitoring, and food industry. The journal also focuses on molecular and supramolecular structures for enhancing device performance.
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