On Chip Protein Pre-Concentration for Enhancing the Sensitivity of Porous Silicon Biosensors

被引:30
作者
Arshaysky-Graham, Sofia [1 ,4 ]
Massad-Ivanir, Naama [1 ]
Paratore, Federico [2 ,5 ]
Scheper, Thomas [4 ]
Bercovici, Moran [2 ,3 ]
Segal, Ester [1 ,3 ]
机构
[1] Technion Israel Inst Technol, Dept Biotechnol & Food Engn, IL-3200003 Haifa, Israel
[2] Technion Israel Inst Technol, Dept Mech Engn, IL-3200003 Haifa, Israel
[3] Technion Israel Inst Technol, Russell Berrie Nanotechnol Inst, IL-3200003 Haifa, Israel
[4] Leibniz Univ Hannover, Inst Tech Chem, Callinstr 5, D-30167 Hannover, NH, Germany
[5] IBM Res Zurich, Saumerstr 4, CH-8803 Ruschlikon, Switzerland
来源
ACS SENSORS | 2017年 / 2卷 / 12期
关键词
porous silicon; optical biosensor; isotachophoresis; aptamer; label-free; FOURIER-TRANSFORM SPECTROSCOPY; OPTICAL BIOSENSORS; PHOTONIC CRYSTALS; ISOTACHOPHORESIS; IMMUNOSENSOR; MICROCAVITIES; IMPROVEMENT; CHEMISTRY; BACTERIA; OPIATES;
D O I
10.1021/acssensors.7b00692
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Porous silicon (PSi) nanomaterials have been widely studied as label-free optical biosensors for protein detection. However, these biosensors' performance, specifically in terms of their sensitivity (which is typically in the micromolar range), is insufficient for many applications. Herein, we present a proof-of-concept application of the electrokinetic isotachophoresis (ITP) technique for real-time preconcentration of a target protein on a PSi biosensor. With ITP, a highly concentrated target zone is delivered to the sensing area, where the protein target is captured by immobilized aptamers. The detection of the binding events is conducted in a label-free manner by reflective interferometric Fourier transformation spectroscopy (RIFTS). Up to 1000-fold enhancement in local concentration of the protein target and the biosensor's sensitivity are achieved, with a measured limit of detection of 7.5 nM. Furthermore, the assay is successfully performed in complex media, such as bacteria lysate samples, while the selectivity of the biosensor is retained. The presented assay could be further utilized for other protein targets, and to promote the development of clinically useful PSi biosensors.
引用
收藏
页码:1767 / 1773
页数:7
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