Friday, January 28, 2011

ISI Web of Knowledge Alert - Hummer, G

ISI Web of Knowledge Citation Alert

Cited Article: Hummer, G. Water conduction through the hydrophobic channel of a carbon nanotube
Alert Expires: 22 AUG 2011
Number of Citing Articles: 3 new records this week (3 in this e-mail)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Title:
Tribological Effects on DNA Translocation in a Nanochannel Coated with a Self-Assembled Monolayer

Authors:
Luan, BQ; Afzali, A; Harrer, S; Peng, HB; Waggoner, P; Polonsky, S; Stolovitzky, G; Martyna, G

Author Full Names:
Luan, Binquan; Afzali, Ali; Harrer, Stefan; Peng, Hongbo; Waggoner, Philip; Polonsky, Stas; Stolovitzky, Gustavo; Martyna, Glenn

Source:
JOURNAL OF PHYSICAL CHEMISTRY B 114 (51): 17172-17176 DEC 30 2010

Language:
English

Document Type:
Article

KeyWords Plus:
MOLECULE MASS-SPECTROMETRY; SOLID-STATE NANOPORE; TRANSPORT; CHANNELS; DYNAMICS; WATER; PROTEINS; FRICTION; PORE

Abstract:
A biomimetic nanochannel coated with a self-assembled monolayer (SAM) can be used for sensing and analyzing biomolecules. The interaction between a transported biomolecule and a SAM governs the mechanically or electrically driven motion of the molecule. To investigate the translocation dynamics of a biomolecule, we performed all-atom molecular dynamics simulations on a single-stranded DNA in a solid-state nanochannel coated with a SAM that consists of octane or octanol polymers. Simulation results demonstrate that the interaction between DNA and a hydrophobic or a hydrophilic SAM is effectively repulsive or adhesive, respectively, resulting in different translocation dynamics of DNA. Therefore, with proper designs of SAMs coated on a channel surface, it is possible to control the translocation dynamics of a biomolecule. This work also demonstrates that traditional tribology methods can be deployed to study a biological, or biomimetic transport process.

Reprint Address:
Luan, BQ, IBM Corp, Thomas J Watson Res Ctr, 1101 Kitchawan Rd, Yorktown Hts, NY 10598 USA.

Research Institution addresses:
[Luan, Binquan; Afzali, Ali; Harrer, Stefan; Peng, Hongbo; Waggoner, Philip; Polonsky, Stas; Stolovitzky, Gustavo; Martyna, Glenn] IBM Corp, Thomas J Watson Res Ctr, Yorktown Hts, NY 10598 USA

E-mail Address:
bluan@us.ibm.com

Cited References:
BEREZHKOVSKII AM, 2005, BIOPHYS J, V88, L17, DOI 10.1529/biophysj.104.057588.
BRANTON D, 2008, NAT BIOTECHNOL, V26, P1146, DOI 10.1038/nbt.1495.
CRUZCHU ER, 2006, J PHYS CHEM B, V110, P21497, DOI 10.1021/jp063896o.
HARRER S, LANGMUIR.
HENRICKSON SE, 2000, PHYS REV LETT, V85, P3057.
HOLMLIN RE, 2001, J AM CHEM SOC, V123, P5075, DOI 10.1021/ja004055c.
HUMMER G, 2001, NATURE, V414, P188.
IQBAL SM, 2007, NAT NANOTECHNOL, V2, P243, DOI 10.1038/nnano.2007.78.
ISRALEWITZ B, 2001, CURR OPIN STRUC BIOL, V11, P224.
JORGENSEN WL, 1983, J CHEM PHYS, V79, P926.
KASIANOWICZ JJ, 1996, P NATL ACAD SCI USA, V93, P13770.
KASIANOWICZ JJ, 2008, ANNU REV ANAL CHEM, V1, P737, DOI 10.1146/annurev.anchem.1.031207.112818.
KEYSER UF, 2006, NAT PHYS, V2, P473, DOI 10.1038/nphys344.
LUAN BQ, 2008, PHYS REV E 1, V78, ARTN 021912.
LUAN BQ, 2010, PHYS REV LETT, V104, ARTN 238103.
LUBENSKY DK, 1999, BIOPHYS J, V77, P1824.
MACKERELL AD, 1998, J PHYS CHEM B, V102, P3586.
NOSONOVSKY M, 2007, MAT SCI ENG R, V58, P162, DOI 10.1016/j.mser.2007.09.001.
PHILLIPS JC, 2005, J COMPUT CHEM, V26, P1781, DOI 10.1002/jcc.20289.
POLONSKY S, 2007, APPL PHYS LETT, V91, ARTN 153103.
REINER JE, 2010, P NATL ACAD SCI USA, V107, P12080, DOI 10.1073/pnas.1002194107.
ROBERTSON JWF, 2007, P NATL ACAD SCI USA, V104, P8207, DOI 10.1073/pnas.0611085104.
STRIOLO A, 2005, J CHEM PHYS, V122, ARTN 234712.
TOMLINSON GA, 1929, PHILOS MAG JUN, V7, P905.
TSUTSUI M, 2010, NAT NANOTECHNOL, V5, P286, DOI 10.1038/nnano.2010.42.
ULMAN A, 1996, CHEM REV, V96, P1533.
WANUNU M, 2007, NANO LETT, V7, P1580, DOI 10.1021/nl070462b.
WONG CTA, 2010, J CHEM PHYS, V133, ARTN 045101.
YAMEEN B, 2009, NANO LETT, V9, P2788, DOI 10.1021/nl901403u.

Cited Reference Count:
29

Times Cited:
0

Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA

Subject Category:
Chemistry, Physical

ISSN:
1520-6106

DOI:
10.1021/jp108865q

IDS Number:
697ZN

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Title:
Structure and adsorption of water in nonuniform cylindrical nanopores

Authors:
Torrie, GM; Lakatos, G; Patey, GN

Author Full Names:
Torrie, G. M.; Lakatos, G.; Patey, G. N.

Source:
JOURNAL OF CHEMICAL PHYSICS 133 (22): Art. No. 224703 DEC 14 2010

Language:
English

Document Type:
Article

KeyWords Plus:
CARBON NANOTUBES; MOLECULAR-DYNAMICS; ICE NANOTUBES; K+ CHANNEL; POTENTIALS; CONDUCTION; IONS

Abstract:
Grand canonical Monte Carlo simulations are used to examine the adsorption and structure of water in the interior of cylindrical nanopores in which the axial symmetry is broken either by varying the radius as a function of position along the pore axis or by introducing regions where the characteristic strength of the water-nanopore interaction is reduced. Using the extended simple point charge (SPC/E) model for water, nanopores with a uniform radius of 6.0 angstrom are found to fill with water at chemical potentials approximately 0.5 kJ/mol higher than the chemical potential of the saturated vapor. The water in these filled pores exists in either a weakly structured fluidlike state or a highly structured uniformly polarized state composed of a series of stacked water clusters with pentagonal cross sections. This highly structured state can be disrupted by creating hydrophobic regions on the surface of the nanopore, and the degree of disruption can be systematically controlled
by adjusting the size of the hydrophobic regions. In particular, hydrophobic banded regions with lengths larger than 9.2 angstrom result in a complete loss of structure and the formation of a liquid-vapor coexistence in the tube interior. Similarly, the introduction of spatial variation in the nanopore radius can produce two condensation transitions at distinct points along the filling isotherm. (C) 2010 American Institute of Physics. [doi:10.1063/1.3505453]

Reprint Address:
Patey, GN, Univ British Columbia, Dept Chem, Vancouver, BC, Canada.

Research Institution addresses:
[Lakatos, G.; Patey, G. N.] Univ British Columbia, Dept Chem, Vancouver, BC, Canada; [Torrie, G. M.] Royal Mil Coll Canada, Dept Chem & Chem Engn, Kingston, ON, Canada

E-mail Address:
torrie-g@rmc.ca; glakatos@chem.ubc.ca; patey@chem.ubc.ca

Cited References:
ANISHKIN A, 2004, BIOPHYS J, V86, P2883.
ARORA G, 2007, NANO LETT, V7, P565, DOI 10.1021/nl062201s.
BECKSTEIN O, 2003, P NATL ACAD SCI USA, V100, P7063, DOI 10.1073/pnas.1136844100.
BECKSTEIN O, 2004, PHYS BIOL, V1, P42, DOI 10.1088/1478-3967/1/1/005.
BERENDSEN HJC, 1987, J PHYS CHEM-US, V91, P6269.
BERNECHE S, 2000, BIOPHYS J, V78, P2900.
BERNECHE S, 2003, P NATL ACAD SCI USA, V100, P8644, DOI 10.1073/pnas.1431750100.
CUMINGS J, 2000, NATURE, V406, P586.
GOLDSMITH J, 2010, J PHYS CHEM LETT, V1, P528, DOI 10.1021/jz900173w.
HOLT JK, 2006, SCIENCE, V312, P1034, DOI 10.1126/science.1126298.
HUMMER G, 2001, NATURE, V414, P188.
JORIO A, 2008, ADV TOPICS SYNTHESIS.
KAKADE BA, 2008, J PHYS CHEM C, V112, P3183, DOI 10.1021/jp711657f.
KOGA K, 2001, NATURE, V412, P802.
KOLESNIKOV AI, 2004, PHYS REV LETT, V93, ARTN 035503.
LAKATOS G, 2007, J CHEM PHYS, V126, ARTN 024703.
LUO CF, 2008, NANO LETT, V8, P2607, DOI 10.1021/nl072642r.
LYNDENBELL RM, 1996, J CHEM PHYS, V105, P9266.
MANIWA Y, 2002, J PHYS SOC JPN, V71, P2863, DOI 10.1143/JPSJ.71.2863.
MILLER SA, 2001, J AM CHEM SOC, V123, P12335.
SAVAGE DF, 2003, PLOS BIOL, V1, P334, ARTN e72.
SONG L, 1996, SCIENCE, V274, P5294.
STRIOLO A, 2005, J CHEM PHYS, V122, ARTN 234712.
STRIOLO A, 2006, J CHEM PHYS, V124, ARTN 074710.
STRIOLO A, 2007, NANOTECHNOLOGY, V18, ARTN 475704.
TAKAIWA D, 2008, P NATL ACAD SCI USA, V105, P39, DOI 10.1073/pnas.0707917105.
TJATJOPOULOS GJ, 1988, J PHYS CHEM-US, V92, P4006.
TRASOBARES S, 2002, J CHEM PHYS, V116, P8966.

Cited Reference Count:
28

Times Cited:
0

Publisher:
AMER INST PHYSICS; CIRCULATION & FULFILLMENT DIV, 2 HUNTINGTON QUADRANGLE, STE 1 N O 1, MELVILLE, NY 11747-4501 USA

Subject Category:
Physics, Atomic, Molecular & Chemical

ISSN:
0021-9606

DOI:
10.1063/1.3505453

IDS Number:
696YR

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Title:
Plugging into Proteins: Poisoning Protein Function by a Hydrophobic Nanoparticle

Authors:
Zuo, GH; Huang, Q; Wei, GH; Zhou, RH; Fang, HP

Author Full Names:
Zuo, Guanghong; Huang, Qing; Wei, Guanghong; Zhou, Ruhong; Fang, Haiping

Source:
ACS NANO 4 (12): 7508-7514 DEC 2010

Language:
English

Document Type:
Article

Author Keywords:
nanoparticle toxicity; protein-nanoparticle interaction; protein function poisoning; hydrophobic interaction; molecular dynamics

KeyWords Plus:
WALLED-CARBON-NANOTUBES; REPLICA EXCHANGE; MULTIDOMAIN PROTEIN; IN-VIVO; MICE; SIMULATION; DYNAMICS; CHANNEL; NANOTECHNOLOGY; RECOGNITION

Abstract:
Nanoscale particles have become promising materials In many fields, such as cancer therapeutics, diagnosis, Imaging, drug delivery, catalysis, as well as biosensors. In order to stimulate and facilitate these applications, there is an urgent need for the understanding of the nanoparticle toxicity and other risks involved with these nanoparticles to human health. In this study, we use large-scale molecular dynamics simulations to study the interaction between several proteins (WW domains) and carbon nanotubes (one form of hydrophobic nanopartides). We have found that the carbon nanotube can plug into the hydrophobic core of proteins to form stable complexes. This plugging of nanotubes disrupts and blocks the active sites of WW domains from binding to the corresponding ligands, thus leading to the loss of the original function of the proteins. The key to this observation is the hydrophobic Interaction between the nanoparticle and the hydrophobic residues, particularly tryptopha
ns, in the core of the domain. We believe that these findings might provide a novel route to the nanopartide toxicity on the molecular level for the hydrophobic nanopartides.

Reprint Address:
Zhou, RH, IBM Corp, Thomas J Watson Res Ctr, Yorktown Hts, NY 10598 USA.

Research Institution addresses:
[Zhou, Ruhong] IBM Corp, Thomas J Watson Res Ctr, Yorktown Hts, NY 10598 USA; [Zuo, Guanghong; Wei, Guanghong; Fang, Haiping] Fudan Univ, T Life Res Ctr, Dept Phys, Shanghai 200433, Peoples R China; [Zuo, Guanghong; Huang, Qing; Fang, Haiping] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China; [Zhou, Ruhong] Columbia Univ, Dept Chem, New York, NY 10027 USA

E-mail Address:
ruhongz@us.ibm.com; fanghaiping@sinap.ac.cn

Cited References:
ALLEN BL, 2008, NANO LETT, V8, P3899, DOI 10.1021/nl802315h.
BRADEN BC, 2000, P NATL ACAD SCI USA, V97, P12193.
CALVARESI M, 2010, ACS NANO, V4, P2283, DOI 10.1021/nn901809b.
CEDERVALL T, 2007, P NATL ACAD SCI USA, V104, P2050, DOI 10.1073/pnas.0608582104.
CHEN Z, 2006, TOXICOL LETT, V163, P109, DOI 10.1016/j.toxlet.2005.10.003.
DILL KA, 1990, BIOCHEMISTRY-US, V29, P7133.
DONALDSON K, 2006, TOXICOL SCI, V92, P5, DOI 10.1093/toxsci/kfj130.
DUAN Y, 1998, SCIENCE, V282, P740.
DUAN Y, 2003, J COMPUT CHEM, V24, P1999, DOI 10.1002/jcc.10349.
GAO YQ, 2005, CELL, V123, P195, DOI 10.1016/j.cell.2005.10.001.
GARCIA AE, 2008, J AM CHEM SOC, V130, P815, DOI 10.1021/ja074191i.
GILBERT N, 2009, NATURE, V460, P937, DOI 10.1038/460937a.
GIOVAMBATTISTA N, 2008, P NATL ACAD SCI USA, V105, P2274, DOI 10.1073/pnas.0708088105.
GONG XJ, 2007, NAT NANOTECHNOL, V2, P709, DOI 10.1038/nnano.2007.320.
HESS B, 2008, J CHEM THEORY COMPUT, V4, P435, DOI 10.1021/ct700301q.
HUA L, 2006, J PHYS CHEM B, V110, P3704, DOI 10.1021/jp055399y.
HUMMER G, 2001, NATURE, V414, P188.
KABSCH W, 1983, BIOPOLYMERS, V22, P2577.
KANG Y, 2008, J PHYS CHEM B, V112, P4801, DOI 10.1021/jp711392g.
KARPLUS M, 2005, PHILOS T A, V363, P355.
KARPLUS M, 2005, PHILOS T ROY SOC A, V363, P331, DOI 10.1098/rsta.2004.1496.
KLEIN J, 2007, P NATL ACAD SCI USA, V104, P2029, DOI 10.1073/pnas.0611610104.
KOLOSNJAJ J, 2007, ADV EXP MED BIOL, V620, P181.
LEVY Y, 2004, P NATL ACAD SCI USA, V101, P511, DOI 10.1073/pnas.2534828100.
LI HK, 2005, ANGEW CHEM INT EDIT, V44, P5100, DOI 10.1002/anie.200500403.
LI JY, 2007, P NATL ACAD SCI USA, V104, P3687, DOI 10.1073/pnas.0604541104.
LI WZ, 1996, SCIENCE, V274, P1701.
LI Z, 2007, ENVIRON HEALTH PERSP, V115, P377, DOI 10.1289/ehp.9688.
LIJIMA S, 1991, NATURE, V354, P56.
LIU P, 2005, NATURE, V437, P159, DOI 10.1038/nature03926.
LIU P, 2006, J PHYS CHEM B, V110, P19018, DOI 10.1021/jp060365r.
MACIAS MJ, 1996, NATURE, V382, P646.
MAHOCK L, 2009, TOXICOL SCI, V112, P468, DOI 10.1093/toxsci/kfp146.
MAYNARD AD, 2004, J TOXICOL ENV HEAL A, V67, P87, DOI 10.1080/15287390490253688.
MAYOR U, 2003, NATURE, V421, P863, DOI 10.1038/nature01428.
MICHALET X, 2005, SCIENCE, V307, P538, DOI 10.1126/science.1104274.
MIRNY L, 2001, ANNU REV BIOPH BIOM, V30, P361.
MITCHELL LA, 2009, NAT NANOTECHNOL, V4, P451, DOI 10.1038/NNANO.2009.151.
MIYASHITA N, 2009, J AM CHEM SOC, V131, P17843, DOI 10.1021/ja905457d.
NEL A, 2006, SCIENCE, V311, P622, DOI 10.1126/science.1114397.
NOON WH, 2002, P NATL ACAD SCI U S2, V99, P6466, DOI 10.1073/pnas.022532599.
PARK KH, 2003, J BIOL CHEM, V278, P50212, DOI 10.1074/jbc.M310216200.
POLAND CA, 2008, NAT NANOTECHNOL, V3, P423, DOI 10.1038/nnano.2008.111.
PORTER AE, 2007, NAT NANOTECHNOL, V2, P713, DOI 10.1038/nnano.2007.347.
ROCKER C, 2009, NAT NANOTECHNOL, V4, P577, DOI 10.1038/NNANO.2009.195.
ROITBERG AE, 2007, J PHYS CHEM B, V111, P2415, DOI 10.1021/jp068335b.
ROSI NL, 2006, SCIENCE, V312, P1027, DOI 10.1126/science.1125559.
RYMANRASMUSSEN JP, 2009, NAT NANOTECHNOL, V4, P747, DOI 10.1038/NNANO.2009.305.
SAVEN JG, 2010, CURR OPIN COLLOID IN, V15, P13, DOI 10.1016/j.cocis.2009.06.002.
SCHIPPER ML, 2008, NAT NANOTECHNOL, V3, P216, DOI 10.1038/nnano.2008.68.
SERVICE RF, 2000, SCIENCE, V290, P1526.
SHEN JW, 2008, BIOMATERIALS, V29, P3847, DOI 10.1016/j.biomaterials.2008.06.013.
SHVEDOVA AA, 2005, AM J PHYSIOL-LUNG C, V289, L698, DOI 10.1152/ajplung.00084.2005.
SNOW CD, 2002, NATURE, V420, P102, DOI 10.1038/nature01160.
TU YS, 2009, P NATL ACAD SCI USA, V106, P18120, DOI 10.1073/pnas.0902676106.
WANG SQ, 2003, NAT MATER, V2, P196, DOI 10.1038/nmat833.
WANG X, 2008, CA-CANCER J CLIN, V58, P97, DOI 10.3322/CA.2007.0003.
XIAO Y, 2003, SCIENCE, V299, P1877.
ZHAO YL, 2008, NAT NANOTECHNOL, V3, P191, DOI 10.1038/nnano.2008.77.
ZHENG LF, 2009, J PHYS CHEM C, V113, P3978, DOI 10.1021/jp809370z.
ZHOU RH, 2004, J MOL GRAPH MODEL, V22, P451, DOI 10.1016/j.jmgm.2003.12.011.
ZHOU RH, 2004, SCIENCE, V305, P1605.
ZHOU RH, 2007, P NATL ACAD SCI USA, V104, P5824, DOI 10.1073/pnas.0701249104.
ZUO GH, 2009, PHYS REV E 1, V79, ARTN 031925.

Cited Reference Count:
64

Times Cited:
0

Publisher:
AMER CHEMICAL SOC; 1155 16TH ST, NW, WASHINGTON, DC 20036 USA

Subject Category:
Chemistry, Multidisciplinary; Nanoscience & Nanotechnology; Materials Science, Multidisciplinary

ISSN:
1936-0851

DOI:
10.1021/nn101762b

IDS Number:
696NW

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Thursday, January 6, 2011

ISI Web of Knowledge Alert - Hummer, G

ISI Web of Knowledge Citation Alert

Cited Article: Hummer, G. Water conduction through the hydrophobic channel of a carbon nanotube
Alert Expires: 22 AUG 2011
Number of Citing Articles: 1 new records this week (1 in this e-mail)
Organization ID: 3b97d1bbc1878baed0ab183d8b03130b
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Note: Instructions on how to purchase the full text of an article and Help Desk Contact information are at the end of the e-mail.
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Title:
Kinetics of water filling the hydrophobic channels of narrow carbon nanotubes studied by molecular dynamics simulations

Authors:
Wu, KF; Zhou, B; Xiu, P; Qi, WP; Wan, RZ; Fang, HP

Author Full Names:
Wu, Kefei; Zhou, Bo; Xiu, Peng; Qi, Wenpeng; Wan, Rongzheng; Fang, Haiping

Source:
JOURNAL OF CHEMICAL PHYSICS 133 (20): Art. No. 204702 NOV 28 2010

Language:
English

Document Type:
Article

KeyWords Plus:
LIQUID WATER; NANOPORES; MECHANISM; COEXISTENCE; PERMEATION; CONDUCTION; TRANSPORT; MEMBRANES; SYSTEMS; ICE

Abstract:
The kinetics of water filling narrow single-walled carbon nanotubes was studied using molecular dynamics simulations. The time required to fully fill a nanotube was linear with respect to the tube length. We observed that water molecules could enter into nanotubes of different lengths, either from one end or from both ends. The probability of having a nanotube filled completely from both ends increased exponentially with the tube length. For short tubes, filling usually proceeded from only one end. For long tubes, filling generally proceeded from both tube ends over three stages, i.e., filling from one end, filling from both ends, and filling from both ends with the dipole reorientation of water molecules to give a concerted ordering within the fully filled tube. The water molecules in the partially filled nanotube were hydrogen bonded similarly to those in the fully filled nanotube. Simulations for the reference Lennard-Jones fluid without hydrogen bonds were also performed
and showed that the filling behavior of water molecules can be attributed to strong intermolecular hydrogen bonding. (C) 2010 American Institute of Physics. [doi:10.1063/1.3509396]

Reprint Address:
Fang, HP, Chinese Acad Sci, Shanghai Inst Appl Phys, POB 800-204, Shanghai 201800, Peoples R China.

Research Institution addresses:
[Wu, Kefei; Zhou, Bo; Qi, Wenpeng; Wan, Rongzheng; Fang, Haiping] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China; [Wu, Kefei; Zhou, Bo] Chinese Acad Sci, Grad Sch, Beijing 100080, Peoples R China; [Xiu, Peng] Zhejiang Univ, Dept Phys, Bio X Lab, Hangzhou 310027, Peoples R China; [Qi, Wenpeng] Shandong Univ, Sch Phys, Jinan 250100, Peoples R China; [Fang, Haiping] CAS, TPCSF, Beijing 100049, Peoples R China

E-mail Address:
fanghaiping@sinap.ac.cn

Cited References:
ABASCAL JLF, 2007, J MOL LIQ, V136, P214, DOI 10.1016/j.molliq.2007.08.025.
ALEXIADIS A, 2008, CHEM REV, V108, P5014, DOI 10.1021/cr078140f.
ALLEN R, 2003, J CHEM PHYS, V119, P3905, DOI 10.1063/1.1590956.
BALL P, 2008, CHEM REV, V108, P74, DOI 10.1021/cr068037a.
BECKSTEIN O, 2001, J PHYS CHEM B, V105, P12902, DOI 10.1021/jp012233y.
BECKSTEIN O, 2003, P NATL ACAD SCI USA, V100, P7063, DOI 10.1073/pnas.1136844100.
BERNE BJ, 2009, ANNU REV PHYS CHEM, V60, P85, DOI 10.1146/annurev.physchem.58.032806.104445.
BONTHUIS DJ, 2009, PHYS REV LETT, V103, ARTN 144503.
BONTHUIS DJ, 2010, LANGMUIR, V26, P12614, DOI 10.1021/la9034535.
BYL O, 2006, J AM CHEM SOC, V128, P12090, DOI 10.1021/ja057856u.
CAMBRE S, 2010, PHYS REV LETT, V104, ARTN 207401.
CORRY B, 2008, J PHYS CHEM B, V112, P1427, DOI 10.1021/jp709845u.
DARDEN T, 1993, J CHEM PHYS, V98, P10089.
DEGROOT BL, 2001, SCIENCE, V294, P2353.
DESOUZA NR, 2006, J PHYS-CONDENS MAT, V18, S2321, DOI 10.1088/0953-8984/18/36/s07.
FANG HP, 2008, J PHYS D APPL PHYS, V41, ARTN 103002.
GONG XJ, 2008, PHYS REV LETT, V101, ARTN 257801.
HANSEN JP, 1969, PHYS REV, V184, P151.
HOLT JK, 2006, SCIENCE, V312, P1034, DOI 10.1126/science.1126298.
HUMMER G, 2001, NATURE, V414, P188.
JORGENSEN WL, 1983, J CHEM PHYS, V79, P926.
JOSEPH S, 2008, NANO LETT, V8, P452, DOI 10.1021/nl072385q.
JOSEPH S, 2008, PHYS REV LETT, V101, ARTN 064502.
KOFINGER J, 2008, P NATL ACAD SCI USA, V105, P13218, DOI 10.1073/pnas.0801448105.
KOGA K, 2001, NATURE, V412, P802.
LINDAHL E, 2001, J MOL MODEL, V7, P306.
LIU B, 2009, NANO LETT, V9, P1386, DOI 10.1021/nl8030339.
LIU J, 2010, J PHYS CHEM A, V114, P2376, DOI 10.1021/jp910624z.
LONGHURST MJ, 2007, PHYS REV LETT, V98, ARTN 145503.
LU HJ, 2008, PHYS REV B, V77, ARTN 174115.
MAJUMDER M, 2005, NATURE, V438, P44, DOI 10.1038/43844a.
MANIWA Y, 2007, NAT MATER, V6, P135, DOI 10.1038/nmat1823.
MUKHERJEE B, 2007, J CHEM PHYS, V126, ARTN 124704.
PANAGIOTOPOULOS AZ, 1994, INT J THERMOPHYS, V15, P1057.
RASAIAH JC, 2008, ANNU REV PHYS CHEM, V59, P713, DOI 10.1146/annurev.physchem.59.032607.093815.
SPARREBOOM W, 2010, NEW J PHYS, V12, ARTN 015004.
STRIOLO A, 2006, NANO LETT, V6, P633, DOI 10.1021/nl052254u.
STRIOLO A, 2007, NANOTECHNOLOGY, V18, ARTN 475704.
THOMAS JA, 2008, NANO LETT, V8, P2788, DOI 10.1021/nl8013617.
TU YS, 2009, P NATL ACAD SCI USA, V106, P18120, DOI 10.1073/pnas.0902676106.
WAGHE A, 2002, J CHEM PHYS, V117, P10789, DOI 10.1063/1.1519861.
WAN RZ, 2009, PHYS CHEM CHEM PHYS, V11, P9898, DOI 10.1039/b907926m.
WANG BY, 2006, J AM CHEM SOC, V128, P15984, DOI 10.1021/ja066431k.
WILDING NB, 1995, PHYS REV E A, V52, P602.
XIU P, 2009, J AM CHEM SOC, V131, P2840, DOI 10.1021/ja804586w.
ZHAO YC, 2008, ADV MATER, V20, P1772, DOI 10.1002/adma.200702956.
ZHOU RH, 2004, SCIENCE, V305, P1605.
ZHU FQ, 2003, BIOPHYS J, V85, P236.

Cited Reference Count:
48

Times Cited:
0

Publisher:
AMER INST PHYSICS; CIRCULATION & FULFILLMENT DIV, 2 HUNTINGTON QUADRANGLE, STE 1 N O 1, MELVILLE, NY 11747-4501 USA

Subject Category:
Physics, Atomic, Molecular & Chemical

ISSN:
0021-9606

DOI:
10.1063/1.3509396

IDS Number:
690LB

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