Detection of target-probe oligonucleotide hybridization using synthetic nanopore resistive pulse sensing

被引:29
作者
Booth, Marsilea Adela [1 ,2 ]
Vogel, Robert [3 ,4 ]
Curran, James M. [1 ]
Harbison, SallyAnn [2 ]
Travas-Sejdic, Jadranka [1 ,2 ]
机构
[1] Univ Auckland, Auckland 92021, New Zealand
[2] Univ Auckland, Inst Environm Sci Res Ltd ESR, Auckland 92021, New Zealand
[3] Izon Sci Ltd, Christchurch 8545, New Zealand
[4] Univ Queensland, Sch Math & Phys, St Lucia, Qld 4072, Australia
关键词
DNA sensor; Resistive pulse sensing; Nanopore; Variable pressure method; SINGLE-STRANDED-DNA; SURFACE-CHARGE; PORE SENSORS; INDIVIDUAL NANOPARTICLES; MAGNETIC NANOPARTICLES; COULTER-COUNTER; TUNABLE PORES; SIZE; MOLECULES; MICROPARTICLES;
D O I
10.1016/j.bios.2013.01.044
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Despite the plethora of DNA sensor platforms available, a portable, sensitive, selective and economic sensor able to rival current fluorescence-based techniques would find use in many applications. In this research, probe oligonucleotide-grafted particles are used to detect target DNA in solution through a resistive pulse nanopore detection technique. Using carbodiimide chemistry, functionalised probe DNA strands are attached to carboxylated dextran-based magnetic particles. Subsequent incubation with complementary target DNA yields a change in surface properties as the two DNA strands hybridize. Particle-by-particle analysis with resistive pulse sensing is performed to detect these changes. A variable pressure method allows identification of changes in the surface charge of particles. As proof-of-principle, we demonstrate that target hybridization is selectively detected at micromolar concentrations (nanomoles of target) using resistive pulse sensing, confirmed by fluorescence and phase analysis light scattering as complementary techniques. The advantages, feasibility and limitations of using resistive pulse sensing for sample analysis are discussed. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:136 / 140
页数:5
相关论文
共 42 条
[1]   Sequence-Specific Recognition of DNA Oligomer Using Peptide Nucleic Acid (PNA)-Modified Synthetic Ion Channels: PNA/DNA Hybridization in Nanoconfined Environment [J].
Ali, Mubarak ;
Neumann, Reinhard ;
Ensinger, Wolfgang .
ACS NANO, 2010, 4 (12) :7267-7274
[2]   Crown ether-electrolyte interactions permit nanopore detection of individual DNA abasic sites in single molecules [J].
An, Na ;
Fleming, Aaron M. ;
White, Henry S. ;
Burrows, Cynthia J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (29) :11504-11509
[3]   The Use of Magnetic Nanoparticles in Analytical Chemistry [J].
Beveridge, Jacob S. ;
Stephens, Jason R. ;
Williams, Mary Elizabeth .
ANNUAL REVIEW OF ANALYTICAL CHEMISTRY, VOL 4, 2011, 4 :251-273
[4]   Effects of Redox Couple on the Response of Polypyrrole-Based Electrochemical DNA Sensors [J].
Booth, Marsilea Adela ;
Harbison, SallyAnn ;
Travas-Sejdic, Jadranka .
ELECTROANALYSIS, 2012, 24 (06) :1311-1317
[5]   Ten years of tension: single-molecule DNA mechanics [J].
Bustamante, C ;
Bryant, Z ;
Smith, SB .
NATURE, 2003, 421 (6921) :423-427
[6]   A resistive-pulse sensor chip for multianalyte immunoassays [J].
Carbonaro, A ;
Sohn, LL .
LAB ON A CHIP, 2005, 5 (10) :1155-1160
[7]  
Clarke J, 2009, NAT NANOTECHNOL, V4, P265, DOI [10.1038/NNANO.2009.12, 10.1038/nnano.2009.12]
[8]   Nanoparticle based enhancement of electrochemical DNA hybridization signal using nanoporous electrodes [J].
de la Escosura-Muniz, Alfredo ;
Merkoci, Arben .
CHEMICAL COMMUNICATIONS, 2010, 46 (47) :9007-9009
[9]   The development of a mRNA multiplex RT-PCR assay for the definitive identification of body fluids [J].
Fleming, Rachel I. ;
Harbison, SallyAnn .
FORENSIC SCIENCE INTERNATIONAL-GENETICS, 2010, 4 (04) :244-256
[10]   Detecting single stranded DNA with a solid state nanopore [J].
Fologea, D ;
Gershow, M ;
Ledden, B ;
McNabb, DS ;
Golovchenko, JA ;
Li, JL .
NANO LETTERS, 2005, 5 (10) :1905-1909