Académique Documents
Professionnel Documents
Culture Documents
If you wish to distribute this article to others, you can order high-quality copies for your
Updated information and services, including high-resolution figures, can be found in the online
version of this article at:
http://www.sciencemag.org/content/338/6109/928.full.html
Supporting Online Material can be found at:
http://www.sciencemag.org/content/suppl/2012/11/15/338.6109.928.DC1.html
A list of selected additional articles on the Science Web sites related to this article can be
found at:
http://www.sciencemag.org/content/338/6109/928.full.html#related
This article cites 31 articles, 8 of which can be accessed free:
http://www.sciencemag.org/content/338/6109/928.full.html#ref-list-1
This article has been cited by 1 articles hosted by HighWire Press; see:
http://www.sciencemag.org/content/338/6109/928.full.html#related-urls
Science (print ISSN 0036-8075; online ISSN 1095-9203) is published weekly, except the last week in December, by the
American Association for the Advancement of Science, 1200 New York Avenue NW, Washington, DC 20005. Copyright
2012 by the American Association for the Advancement of Science; all rights reserved. The title Science is a
registered trademark of AAAS.
RESEARCH ARTICLE
forest are twist-spun into a yarn (7–14). The utilized
forests are ~350 mm high and consist of MWNTs that
Electrically, Chemically, and Photonically have an outer diameter of ~9 nm, contain about six
walls, and form large bundles. Symmetric twist in-
Powered Torsional and Tensile Actuation sertion during sheet draw from a forest or into a
predrawn nanotube sheet (suspended between either
of Hybrid Carbon Nanotube Yarn Muscles a forest and one rigid support or two rigid supports)
provides the two investigated helical yarn structures
(Fermat scrolls for the former cases and dual-
Márcio D. Lima,1* Na Li,1,2* Mônica Jung de Andrade,1 Shaoli Fang,1 Jiyoung Oh,1 Archimedean scrolls for the latter) (15, 16) illus-
Geoffrey M. Spinks,3 Mikhail E. Kozlov,1 Carter S. Haines,1 Dongseok Suh,1 trated in Fig. 1, H and I. The bias angle (the angle
Javad Foroughi,3 Seon Jeong Kim,4 Yongsheng Chen,2 Taylor Ware,1 Min Kyoon Shin,4 between the yarn length and nanotube directions)
Leonardo D. Machado,5 Alexandre F. Fonseca,6 John D. W. Madden,7 Walter E. Voit,1 for the simpler Fermat yarn is
Douglas S. Galvão,5 Ray H. Baughman1†
a = tan−1(2prT ) (1)
Artificial muscles are of practical interest, but few types have been commercially exploited. Typical where r is the distance from yarn center and T is
problems include slow response, low strain and force generation, short cycle life, use of electrolytes, the inserted twist in turns per yarn length. The mea-
A -5 B -8
-0.12
0.15
Tensile actuation (%)
-7
-4 -0.08
-6
Tensile actuation (%)
-0.04
-3 -5 -8
0.00 0.09
Tensile actuation (%)
30 60 90 120 150
-4 -6
o
Temperature ( C)
-2
-3 -4 0.06
-2 -2
-1
0.03
-1 0
0 500 1000 1500 2000 2500
o
Temperature ( C)
0 0 0.00
25 50 75 100 125 150 175 200 0 2 4 6 8 10 12 14 16 18 20
o
Temperature ( C) Electrical power (W/cm)
Fig. 2. Thermal tensile actuation for two-end–tethered homochiral yarns. (A) thermal tensile actuation strain and work capacity during contraction in vacuum
Tensile actuation strain versus temperature before (black) and after (red) wax as a function of applied electrical power for a neat, coiled, dual-Archimedean
infiltration for a coiled, dual-Archimedean yarn having 130-mm initial diameter, yarn having 115-mm diameter and the inserted twist of the dual-Archimedean
an inserted twist of ~4000 turns/m (per length of the precursor sheet stack), and yarn in (A). Insets: Tensile actuation versus estimated temperature for this yarn
an applied stress of 6.8 MPa. Inset: Corresponding actuation data before (black) (left) and photograph of the incandescent yarn lifting a 10-g load. Closed
and after (red) wax infiltration for a noncoiled Fermat yarn having 16-mm initial symbols and open symbols in (A) and (B) are for increasing and decreasing
diameter, ~20,000 turns/m twist, and an applied stress of 4.8 MPa. (B) Electro- temperature, respectively.
A C
-6
Yarn 2517 turns/m
Fig. 3. Electrothermal
-3 1.4
tensile actuation for two-
Coil 3990 turns/m
Coil 4263 turns/m end–tethered, homochiral,
-5
1.2
Work capacity (kJ/kg)
Tensile actuation (%)
1 B 0.4
18.3-V/cm, 20-Hz symmet-
-1 ric square wave voltage
0.2
0
while lifting a load that
0 0.0 provided a 14.3-MPa stress.
0 10 20 30 40 50 60 70 80 90
(B) Tensile actuation for
-1 Stress (MPa) the yarn of (A) with 109-
MPa applied tensile stress
0.0 0.5 1.0 1.5 2.0 2.5 3.0 when driven at 3% duty cycle by 15-ms, 32-V/cm square-wave voltage pulses having a period
-12 of 500 ms. (C) The stress dependence of steady-state tensile actuation and contractile work
D (black and blue data points, respectively) produced by Joule heating (0.189 V/cm) for a
-9
150-mm-diameter, dual-Archimedean yarn having different levels of inserted twist. (D) Tensile
-6
strain versus time for the yarn of (C) with 3990 turns/m of inserted twist per precursor sheet
stack length, when supporting a 5.5-MPa tensile stress and driven by a 15-V/cm square wave
-3 having 50-ms pulse duration and 2.5-s period.
0
0 1 2 3 4 5 6
Time (s)
12
Average rotation speed (1000 rpm)
5 12
average speed was 7600 revolutions/min. (C) Static torque versus applied electrical power for
a 100-mm-diameter, 6.4-cm-long, fully infiltrated, heterochiral, dual-Archimedean yarn
having ~3000 turns/m of inserted twist per stack length. Insets: Greco-Roman catapult 6
configuration used for torque measurements (bottom) and photograph indicating the
melting temperature of a paraffin flake applied to the yarn surface (top left).
4
0
0 20 40 60 80 100
Electrical power (mW/cm)
REPORTS
from DNA and anchored to a lipid membrane by
Synthetic Lipid Membrane Channels cholesterol side chains. The shape of our syn-
thetic channel is inspired by the natural channel
protein a-hemolysin (2), although there are dif-
Formed by Designed DNA Nanostructures ferences in physical properties such as charge,
hydrophobicity, and size.
Martin Langecker,1* Vera Arnaut,1* Thomas G. Martin,2* Jonathan List,1 Stephan Renner,1 We constructed the channel by means of mo-
Michael Mayer,3 Hendrik Dietz,2† Friedrich C. Simmel1† lecular self-assembly with scaffolded DNA ori-
We created nanometer-scale transmembrane channels in lipid bilayers by means of self-assembled gami (3–9) (Fig. 1A). The channel consists of
DNA-based nanostructures. Scaffolded DNA origami was used to create a stem that penetrated and spanned two modules: (i) a stem that penetrates and spans
a lipid membrane, as well as a barrel-shaped cap that adhered to the membrane, in part via 26 cholesterol a lipid membrane, and (ii) a barrel-shaped cap
moieties. In single-channel electrophysiological measurements, we found similarities to the response of
natural ion channels, such as conductances on the order of 1 nanosiemens and channel gating. More 1
Lehrstuhl für Bioelektronik, Physics Department and ZNN/WSI,
pronounced gating was seen for mutations in which a single DNA strand of the stem protruded into the Technische Universität München, 85748 Garching, Germany.
2
channel. Single-molecule translocation experiments show that the synthetic channels can be used to Walter Schottky Institute, Physics Department, Technische Uni-
discriminate single DNA molecules. versität München, 85748 Garching, Germany. 3Department of
Biomedical Engineering, University of Michigan, Ann Arbor, MI
48109, USA.
large class of proteins and peptides form or other entities through the otherwise imper-