Cited Article: Holt JK. Fast mass transport through sub-2-nanometer carbon nanotubes
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AU Liu, HT
He, J
Tang, JY
Liu, H
Pang, P
Cao, D
Krstic, P
Joseph, S
Lindsay, S
Nuckolls, C
AF Liu, Haitao
He, Jin
Tang, Jinyao
Liu, Hao
Pang, Pei
Cao, Di
Krstic, Predrag
Joseph, Sony
Lindsay, Stuart
Nuckolls, Colin
TI Translocation of Single-Stranded DNA Through Single-Walled Carbon
Nanotubes
SO SCIENCE
LA English
DT Article
ID SOLID-STATE NANOPORES; TRANSPORT; MOLECULES; CHANNEL; FABRICATION;
MEMBRANES; ACID
AB We report the fabrication of devices in which one single-walled carbon
nanotube spans a barrier between two fluid reservoirs, enabling direct
electrical measurement of ion transport through the tube. A fraction of
the tubes pass anomalously high ionic currents. Electrophoretic
transport of small single-stranded DNA oligomers through these tubes is
marked by large transient increases in ion current and was confirmed by
polymerase chain reaction analysis. Each current pulse contains about
10(7) charges, an enormous amplification of the translocated charge.
Carbon nanotubes simplify the construction of nanopores, permit new
types of electrical measurements, and may open avenues for control of
DNA translocation.
C1 [He, Jin; Liu, Hao; Pang, Pei; Cao, Di; Lindsay, Stuart] Biodesign Inst, Tempe, AZ 85287 USA.
[Liu, Haitao; Tang, Jinyao; Nuckolls, Colin] Columbia Univ, Dept Chem, New York, NY 10027 USA.
[Liu, Hao; Lindsay, Stuart] Dept Chem & Biochem, Tempe, AZ 85287 USA.
[Pang, Pei; Cao, Di; Lindsay, Stuart] Arizona State Univ, Dept Phys, Tempe, AZ 85287 USA.
[Krstic, Predrag; Joseph, Sony] Oak Ridge Natl Lab, Div Phys, Oak Ridge, TN 37831 USA.
RP Lindsay, S, Biodesign Inst, Tempe, AZ 85287 USA.
EM Stuart.Lindsay@asu.edu
cn37@columbia.edu
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NR 26
TC 0
PU AMER ASSOC ADVANCEMENT SCIENCE; 1200 NEW YORK AVE, NW, WASHINGTON, DC
20005 USA
SN 0036-8075
DI 10.1126/science.1181799
PD JAN 1
VL 327
IS 5961
BP 64
EP 67
SC Multidisciplinary Sciences
GA 541DZ
UT ISI:000273395400030
ER
PT J
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AU Titov, AV
Wang, BY
Sint, K
Kral, P
AF Titov, Alexey V.
Wang, Boyang
Sint, Kyaw
Kral, Petr
TI Controllable Synthetic Molecular Channels: Biomimetic Ammonia Switch
SO JOURNAL OF PHYSICAL CHEMISTRY B
LA English
DT Article
ID FUNCTIONALIZED CARBON NANOTUBES; AQUAPORIN WATER CHANNELS; ION
CHANNELS; DYNAMICS SIMULATIONS; PEPTIDE NANOTUBES; FLOWING LIQUIDS; GAS
SEPARATION; K+ CHANNEL; PROTEIN; DESIGN
AB We use molecular dynamics simulations combined with iterative screening
to test if one can design mechanically controllable and selective
molecular pores. The first model pore is formed by two stacked carbon
nanocones connected by aliphatic chains at their open tips, in analogy
to aquaporins. It turns out that when one nanocone is gradually rotated
with respect to the other, the molecular chains alter the size of the
nanopore formed at the cone tips and control the flow rates of liquid
pentane through it. The second model pore is formed by two carbon
nanotubes joined by a cylindrical structure of antiparallel peptides.
By application of a torque to one of the nanotubes, while holding the
other, we can reversibly fold the peptides into forward or
backward-twisted barrels. We have modified the internal residues in
these barrels to make these pores selective and controllable.
Eventually, we found a nanopore that in the two folded configurations
has very different transmission rates for hydrated NH3 molecules.
C1 [Titov, Alexey V.; Wang, Boyang; Sint, Kyaw; Kral, Petr] Univ Illinois, Dept Chem, Chicago, IL 60607 USA.
RP Kral, P, Univ Illinois, Dept Chem, Chicago, IL 60607 USA.
EM pkral@uic.edu
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NR 67
TC 0
PU AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
SN 1520-6106
DI 10.1021/jp9103933
PD JAN 21
VL 114
IS 2
BP 1174
EP 1179
SC Chemistry, Physical
GA 541HD
UT ISI:000273405000059
ER
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