8th All-Russian Conference on Low Temperature Plasma in the Processes of Functional Coating Preparation | |
Formation of sensor array on the AFM chip surface by magnetron sputtering | |
Shumov, I.D.^1 ; Kanashenko, S.L.^1 ; Ziborov, V.S.^2 ; Ivanov, Yu D.^1 ; Archakov, A.I.^1 ; Pleshakova, T.O.^1 | |
Institute of Biomedical Chemistry, Moscow, Russia^1 | |
Joint Institute for High Temperatures RAS, Moscow, Russia^2 | |
关键词: Biological fluids; Biomedical research; Buffer solutions; Diagnostic applications; Highly sensitive detections; Molecular detectors; Protein analysis; Protein detection; | |
Others : https://iopscience.iop.org/article/10.1088/1742-6596/789/1/012053/pdf DOI : 10.1088/1742-6596/789/1/012053 |
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来源: IOP | |
【 摘 要 】
Development of atomic force microscopy (AFM)-based nanotechnological approaches to highly sensitive detection of proteins is a perspective direction in biomedical research. These approaches use AFM chips to concentrate the target proteins from the test solution volume (buffer solution, diluted biological fluid) onto the chip surface for their subsequent registration on the chip surface by AFM. Atomic force microscope is a molecular detector that enables protein detection at ultra-low (subfemtomolar) concentrations in single-molecule counting mode. Due to extremely high sensitivity of AFM, its application for multiplexed protein detection is of great interest for use in proteomics and diagnostic applications. In this study, AFM chips containing an array of sensor areas have been fabricated. Magnetron sputtering of chromium and tungsten nanolayers has been used to form optically visible metallic marks on the AFM chip surface to provide necessary precision of AFM probe positioning against each sensor area for scanning. It has been demonstrated that the marks formed by magnetron sputtering of Cr and W are stable on the surface of the AFM chips during the following activation and intensive washing of this surface. The results obtained in our present study allow application of the developed chips for multiplexed protein analysis by AFM.
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