Nanopore extended field effect transistor for selective
single molecule biosensing
single molecule biosensing
File(s)s41467-017-00549-w.pdf (3.2 MB)
Published version
Author(s)
Type
Journal Article
Abstract
There has been a significant drive to deliver nanotechnological solutions to biosensing, yet there remains an unmet need in the development of biosensors that are affordable, integrated, fast, capable of multiplexed detection, and offer high selectivity for trace analyte detection in biological fluids. Herein, some of these challenges are addressed by designing a new class of nanoscale sensors dubbed nanopore extended field-effect transistor (nexFET) that combine the advantages of nanopore single-molecule sensing, field-effect transistors, and recognition chemistry. We report on a polypyrrole functionalized nexFET, with controllable gate voltage that can be used to switch on/off, and slow down single-molecule DNA transport through a nanopore. This strategy enables higher molecular throughput, enhanced signal-to-noise, and even heightened selectivity via functionalization with an embedded receptor. This is shown for selective sensing of an anti-insulin antibody in the presence of its IgG isotype.
Date Issued
2017-09-19
Date Acceptance
2017-07-11
Citation
Nature Communications, 2017, 8, pp.1-9
ISSN
2041-1723
Publisher
Nature Publishing Group
Start Page
1
End Page
9
Journal / Book Title
Nature Communications
Volume
8
Copyright Statement
This article is licensed under a Creative Commons
Attribution 4.0 International License, which permits use, sharing,
adaptation, distribution and reproduction in any medium or format, as long as you give
appropriate credit to the original author(s) and the source, provide a link to the Creative
Commons license, and indicate if changes were made. The images or other third party
material in this article are included in the article’s Creative Commons license, unless
indicated otherwise in a credit line to the material. If material is not included in the
article’s Creative Commons license and your intended use is not permitted by statutory
regulation or exceeds the permitted use, you will need to obtain permission directly from
the copyright holder. To view a copy of this license, visit http://creativecommons.org/
licenses/by/4.0/.
© The Author(s) 2017
Attribution 4.0 International License, which permits use, sharing,
adaptation, distribution and reproduction in any medium or format, as long as you give
appropriate credit to the original author(s) and the source, provide a link to the Creative
Commons license, and indicate if changes were made. The images or other third party
material in this article are included in the article’s Creative Commons license, unless
indicated otherwise in a credit line to the material. If material is not included in the
article’s Creative Commons license and your intended use is not permitted by statutory
regulation or exceeds the permitted use, you will need to obtain permission directly from
the copyright holder. To view a copy of this license, visit http://creativecommons.org/
licenses/by/4.0/.
© The Author(s) 2017
License URL
Sponsor
Commission of the European Communities
Engineering & Physical Science Research Council (EPSRC)
Commission of the European Communities
Commission of the European Communities
Biotechnology and Biological Sciences Research Council (BBSRC)
Imperial College London
Engineering and Physical Sciences Research Council
Identifier
https://www.nature.com/articles/s41467-017-00549-w
Grant Number
724300
EP/P011985/1
279818
677677
BB/L017865/1
EP/L015277/1
Subjects
Science & Technology
Multidisciplinary Sciences
Science & Technology - Other Topics
ELECTRONIC DETECTION
DNA
SENSORS
TRANSLOCATION
PROTEINS
DELIVERY
RECEPTOR
Biosensing Techniques
DNA
Insulin
Nanopores
Nanostructures
Nanotechnology
Sensitivity and Specificity
Insulin
DNA
Sensitivity and Specificity
Biosensing Techniques
Nanotechnology
Nanostructures
Nanopores
Publication Status
Published
Article Number
586
Date Publish Online
2017-09-19