TY - JOUR
T1 - Interference-Free Detection of Genetic Biomarkers Using Synthetic Dipole-Facilitated Nanopore Dielectrophoresis
AU - Tian, Kai
AU - Decker, Karl
AU - Aksimentiev, Aleksei
AU - Gu, Li Qun
N1 - Funding Information:
This work was supported by grants from the National Institutes of Health (R01-GM079613 and R01-GM114204 to L.-Q.G. and A.A.). The authors acknowledge supercomputer time at the Blue Waters Sustained Petascale Facility (University of Illinois) and at the Texas Advanced Computing Center (Stampede, allocation award MCA05S028).
Publisher Copyright:
© 2016 American Chemical Society.
PY - 2017/2/28
Y1 - 2017/2/28
N2 - The motion of polarizable particles in a nonuniform electric field (i.e., dielectrophoresis) has been extensively used for concentration, separation, sorting, and transport of biological particles from cancer cells and viruses to biomolecules such as DNAs and proteins. However, current approaches to dielectrophoretic manipulation are not sensitive enough to selectively target individual molecular species. Here, we describe the application of the dielectrophoretic principle for selective detection of DNA and RNA molecules using an engineered biological nanopore. The key element of our approach is a synthetic polycationic nanocarrier that selectively binds to the target biomolecules, dramatically increasing their dielectrophoretic response to the electric field gradient generated by the nanopore. The dielectrophoretic capture of the nanocarrier-target complexes is detected as a transient blockade of the nanopore ionic current, while any nontarget nucleic acids are repelled from the nanopore by electrophoresis and thus do not interfere with the signal produced by the target's capture. Strikingly, we show that even modestly charged nanocarriers can be used to capture DNA or RNA molecules of any length or secondary structure and simultaneously detect several molecular targets. Such selective, multiplex molecular detection technology would be highly desirable for real-time analysis of complex clinical samples.
AB - The motion of polarizable particles in a nonuniform electric field (i.e., dielectrophoresis) has been extensively used for concentration, separation, sorting, and transport of biological particles from cancer cells and viruses to biomolecules such as DNAs and proteins. However, current approaches to dielectrophoretic manipulation are not sensitive enough to selectively target individual molecular species. Here, we describe the application of the dielectrophoretic principle for selective detection of DNA and RNA molecules using an engineered biological nanopore. The key element of our approach is a synthetic polycationic nanocarrier that selectively binds to the target biomolecules, dramatically increasing their dielectrophoretic response to the electric field gradient generated by the nanopore. The dielectrophoretic capture of the nanocarrier-target complexes is detected as a transient blockade of the nanopore ionic current, while any nontarget nucleic acids are repelled from the nanopore by electrophoresis and thus do not interfere with the signal produced by the target's capture. Strikingly, we show that even modestly charged nanocarriers can be used to capture DNA or RNA molecules of any length or secondary structure and simultaneously detect several molecular targets. Such selective, multiplex molecular detection technology would be highly desirable for real-time analysis of complex clinical samples.
KW - HIV-TAT
KW - microRNA
KW - molecular dynamics simulation
KW - nucleic acids
KW - single-molecule detection
KW - single-nucleotide polymorphism
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U2 - 10.1021/acsnano.6b07570
DO - 10.1021/acsnano.6b07570
M3 - Article
C2 - 28036167
AN - SCOPUS:85014146399
VL - 11
SP - 1204
EP - 1213
JO - ACS Nano
JF - ACS Nano
SN - 1936-0851
IS - 2
ER -