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

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Sofia Arshavsky-Graham
  • Naama Massad-Ivanir
  • Federico Paratore
  • Thomas Scheper
  • Moran Bercovici
  • Ester Segal

Research Organisations

External Research Organisations

  • Technion-Israel Institute of Technology
  • IBM Zurich Research Laboratory
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Details

Original languageEnglish
Pages (from-to)1767-1773
Number of pages7
JournalACS SENSORS
Volume2
Issue number12
Publication statusPublished - 22 Nov 2017

Abstract

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.

Keywords

    aptamer, isotachophoresis, label-free, optical biosensor, porous silicon

ASJC Scopus subject areas

Cite this

On Chip Protein Pre-Concentration for Enhancing the Sensitivity of Porous Silicon Biosensors. / Arshavsky-Graham, Sofia; Massad-Ivanir, Naama; Paratore, Federico et al.
In: ACS SENSORS, Vol. 2, No. 12, 22.11.2017, p. 1767-1773.

Research output: Contribution to journalArticleResearchpeer review

Arshavsky-Graham, S, Massad-Ivanir, N, Paratore, F, Scheper, T, Bercovici, M & Segal, E 2017, 'On Chip Protein Pre-Concentration for Enhancing the Sensitivity of Porous Silicon Biosensors', ACS SENSORS, vol. 2, no. 12, pp. 1767-1773. https://doi.org/10.1021/acssensors.7b00692
Arshavsky-Graham, S., Massad-Ivanir, N., Paratore, F., Scheper, T., Bercovici, M., & Segal, E. (2017). On Chip Protein Pre-Concentration for Enhancing the Sensitivity of Porous Silicon Biosensors. ACS SENSORS, 2(12), 1767-1773. https://doi.org/10.1021/acssensors.7b00692
Arshavsky-Graham S, Massad-Ivanir N, Paratore F, Scheper T, Bercovici M, Segal E. On Chip Protein Pre-Concentration for Enhancing the Sensitivity of Porous Silicon Biosensors. ACS SENSORS. 2017 Nov 22;2(12):1767-1773. doi: 10.1021/acssensors.7b00692
Arshavsky-Graham, Sofia ; Massad-Ivanir, Naama ; Paratore, Federico et al. / On Chip Protein Pre-Concentration for Enhancing the Sensitivity of Porous Silicon Biosensors. In: ACS SENSORS. 2017 ; Vol. 2, No. 12. pp. 1767-1773.
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title = "On Chip Protein Pre-Concentration for Enhancing the Sensitivity of Porous Silicon Biosensors",
abstract = "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.",
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AU - Arshavsky-Graham, Sofia

AU - Massad-Ivanir, Naama

AU - Paratore, Federico

AU - Scheper, Thomas

AU - Bercovici, Moran

AU - Segal, Ester

N1 - Funding information: This work was partially supported by the NEVET grant administrated by the Russell Berrie Nanotechnology Institute (RBNI), by the German Research Foundation under the grant SCHE 279/32-1 and by the Initial Training Network, Virtual Vials, funded by the FP7 Marie Curie Actions of the European Commission (FP7-PEOPLE-2013-ITN-607322). The oxidation process was performed at the Micro-Nano Fabrication Unit (MNFU), Technion. The authors thank Dr. Khaled Gommed for his assistance in preparation of the microfluidic channels and Prof. Yuval Shoham from the Department of Biotechnology and Food Engineering at the Technion for supplying the target protein. S.A.-G. is most grateful for the Miriam and Aaron Gutwirth scholarship and for TEVA Pharmaceutical Industries Excellence Scholarship for M.Sc. students in Analytical Chemistry.

PY - 2017/11/22

Y1 - 2017/11/22

N2 - 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.

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