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Polymer translocation through a nanopore under an applied external field
We investigate the dynamics of polymer translocation through a nanopore under an externally applied field using the two-dimensional fluctuating bond model with single-segment Monte Carlo moves. We concentrate on the influence of the field strength E , length of the chain N , and length of the pore L...
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Published in: | The Journal of chemical physics 2006-03, Vol.124 (11), p.114704-114704-7 |
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container_end_page | 114704-7 |
container_issue | 11 |
container_start_page | 114704 |
container_title | The Journal of chemical physics |
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creator | Luo, Kaifu Huopaniemi, Ilkka Ala-Nissila, Tapio Ying, See-Chen |
description | We investigate the dynamics of polymer translocation through a nanopore under an externally applied field using the two-dimensional fluctuating bond model with single-segment Monte Carlo moves. We concentrate on the influence of the field strength
E
, length of the chain
N
, and length of the pore
L
on forced translocation. As our main result, we find a crossover scaling for the translocation time
τ
with the chain length from
τ
∼
N
2
ν
for relatively short polymers to
τ
∼
N
1
+
ν
for longer chains, where
ν
is the Flory exponent. We demonstrate that this crossover is due to the change in the dependence of the translocation velocity
v
on the chain length. For relatively short chains
v
∼
N
−
ν
, which crosses over to
v
∼
N
−
1
for long polymers. The reason for this is that with increasing
N
there is a high density of segments near the exit of the pore, which slows down the translocation process due to slow relaxation of the chain. For the case of a long nanopore for which
R
||
, the radius of gyration
R
g
along the pore, is smaller than the pore length, we find no clear scaling of the translocation time with the chain length. For large
N
, however, the asymptotic scaling
τ
∼
N
1
+
ν
is recovered. In this regime,
τ
is almost independent of
L
. We have previously found that for a polymer, which is initially placed in the middle of the pore, there is a minimum in the escape time for
R
||
≈
L
. We show here that this minimum persists for weak fields
E
such that
E
L
is less than some critical value, but vanishes for large values of
E
L
. |
doi_str_mv | 10.1063/1.2179792 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67783222</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67783222</sourcerecordid><originalsourceid>FETCH-LOGICAL-c439t-48e77f860d78d981234163e0b917865dc4f956c6ec9561ac52eb6dfdd19504ba3</originalsourceid><addsrcrecordid>eNp10DFLxDAYxvEgineeDn4BySQ49EzSNmkWQQ71hAMddA5p8tartElNWvC-vdUr6OL0LD-e4Y_QOSVLSnh6TZeMCikkO0BzSgqZCC7JIZoTwmgiOeEzdBLjOyGECpYdoxnleZ5LIuZo_eybXQsB90G72Hij-9o73G-DH962WGOnne98ADw4OzLtsO66pgaL4bOH4HSDqxoae4qOKt1EOJt2gV7v715W62Tz9PC4ut0kJktln2QFCFEVnFhRWFlQlmaUp0BKSUXBc2uySubccDDjUG1yBiW3lbVU5iQrdbpAl_vfLviPAWKv2joaaBrtwA9RcSGKlDE2wqs9NMHHGKBSXahbHXaKEvWdTVE1ZRvtxXQ6lC3YXzl1GsHNHkRT9z-J_n-biqq_RdMvt9V9Bw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67783222</pqid></control><display><type>article</type><title>Polymer translocation through a nanopore under an applied external field</title><source>American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list)</source><source>American Institute of Physics</source><creator>Luo, Kaifu ; Huopaniemi, Ilkka ; Ala-Nissila, Tapio ; Ying, See-Chen</creator><creatorcontrib>Luo, Kaifu ; Huopaniemi, Ilkka ; Ala-Nissila, Tapio ; Ying, See-Chen</creatorcontrib><description>We investigate the dynamics of polymer translocation through a nanopore under an externally applied field using the two-dimensional fluctuating bond model with single-segment Monte Carlo moves. We concentrate on the influence of the field strength
E
, length of the chain
N
, and length of the pore
L
on forced translocation. As our main result, we find a crossover scaling for the translocation time
τ
with the chain length from
τ
∼
N
2
ν
for relatively short polymers to
τ
∼
N
1
+
ν
for longer chains, where
ν
is the Flory exponent. We demonstrate that this crossover is due to the change in the dependence of the translocation velocity
v
on the chain length. For relatively short chains
v
∼
N
−
ν
, which crosses over to
v
∼
N
−
1
for long polymers. The reason for this is that with increasing
N
there is a high density of segments near the exit of the pore, which slows down the translocation process due to slow relaxation of the chain. For the case of a long nanopore for which
R
||
, the radius of gyration
R
g
along the pore, is smaller than the pore length, we find no clear scaling of the translocation time with the chain length. For large
N
, however, the asymptotic scaling
τ
∼
N
1
+
ν
is recovered. In this regime,
τ
is almost independent of
L
. We have previously found that for a polymer, which is initially placed in the middle of the pore, there is a minimum in the escape time for
R
||
≈
L
. We show here that this minimum persists for weak fields
E
such that
E
L
is less than some critical value, but vanishes for large values of
E
L
.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.2179792</identifier><identifier>PMID: 16555907</identifier><identifier>CODEN: JCPSA6</identifier><language>eng</language><publisher>United States: American Institute of Physics</publisher><subject>Electromagnetic Fields ; Models, Chemical ; Nanostructures - chemistry ; Nucleic Acids - chemistry ; Polymers - chemistry ; Proteins - chemistry</subject><ispartof>The Journal of chemical physics, 2006-03, Vol.124 (11), p.114704-114704-7</ispartof><rights>2006 American Institute of Physics</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-48e77f860d78d981234163e0b917865dc4f956c6ec9561ac52eb6dfdd19504ba3</citedby><cites>FETCH-LOGICAL-c439t-48e77f860d78d981234163e0b917865dc4f956c6ec9561ac52eb6dfdd19504ba3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,778,780,791,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16555907$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luo, Kaifu</creatorcontrib><creatorcontrib>Huopaniemi, Ilkka</creatorcontrib><creatorcontrib>Ala-Nissila, Tapio</creatorcontrib><creatorcontrib>Ying, See-Chen</creatorcontrib><title>Polymer translocation through a nanopore under an applied external field</title><title>The Journal of chemical physics</title><addtitle>J Chem Phys</addtitle><description>We investigate the dynamics of polymer translocation through a nanopore under an externally applied field using the two-dimensional fluctuating bond model with single-segment Monte Carlo moves. We concentrate on the influence of the field strength
E
, length of the chain
N
, and length of the pore
L
on forced translocation. As our main result, we find a crossover scaling for the translocation time
τ
with the chain length from
τ
∼
N
2
ν
for relatively short polymers to
τ
∼
N
1
+
ν
for longer chains, where
ν
is the Flory exponent. We demonstrate that this crossover is due to the change in the dependence of the translocation velocity
v
on the chain length. For relatively short chains
v
∼
N
−
ν
, which crosses over to
v
∼
N
−
1
for long polymers. The reason for this is that with increasing
N
there is a high density of segments near the exit of the pore, which slows down the translocation process due to slow relaxation of the chain. For the case of a long nanopore for which
R
||
, the radius of gyration
R
g
along the pore, is smaller than the pore length, we find no clear scaling of the translocation time with the chain length. For large
N
, however, the asymptotic scaling
τ
∼
N
1
+
ν
is recovered. In this regime,
τ
is almost independent of
L
. We have previously found that for a polymer, which is initially placed in the middle of the pore, there is a minimum in the escape time for
R
||
≈
L
. We show here that this minimum persists for weak fields
E
such that
E
L
is less than some critical value, but vanishes for large values of
E
L
.</description><subject>Electromagnetic Fields</subject><subject>Models, Chemical</subject><subject>Nanostructures - chemistry</subject><subject>Nucleic Acids - chemistry</subject><subject>Polymers - chemistry</subject><subject>Proteins - chemistry</subject><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp10DFLxDAYxvEgineeDn4BySQ49EzSNmkWQQ71hAMddA5p8tartElNWvC-vdUr6OL0LD-e4Y_QOSVLSnh6TZeMCikkO0BzSgqZCC7JIZoTwmgiOeEzdBLjOyGECpYdoxnleZ5LIuZo_eybXQsB90G72Hij-9o73G-DH962WGOnne98ADw4OzLtsO66pgaL4bOH4HSDqxoae4qOKt1EOJt2gV7v715W62Tz9PC4ut0kJktln2QFCFEVnFhRWFlQlmaUp0BKSUXBc2uySubccDDjUG1yBiW3lbVU5iQrdbpAl_vfLviPAWKv2joaaBrtwA9RcSGKlDE2wqs9NMHHGKBSXahbHXaKEvWdTVE1ZRvtxXQ6lC3YXzl1GsHNHkRT9z-J_n-biqq_RdMvt9V9Bw</recordid><startdate>20060321</startdate><enddate>20060321</enddate><creator>Luo, Kaifu</creator><creator>Huopaniemi, Ilkka</creator><creator>Ala-Nissila, Tapio</creator><creator>Ying, See-Chen</creator><general>American Institute of Physics</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20060321</creationdate><title>Polymer translocation through a nanopore under an applied external field</title><author>Luo, Kaifu ; Huopaniemi, Ilkka ; Ala-Nissila, Tapio ; Ying, See-Chen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-48e77f860d78d981234163e0b917865dc4f956c6ec9561ac52eb6dfdd19504ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Electromagnetic Fields</topic><topic>Models, Chemical</topic><topic>Nanostructures - chemistry</topic><topic>Nucleic Acids - chemistry</topic><topic>Polymers - chemistry</topic><topic>Proteins - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luo, Kaifu</creatorcontrib><creatorcontrib>Huopaniemi, Ilkka</creatorcontrib><creatorcontrib>Ala-Nissila, Tapio</creatorcontrib><creatorcontrib>Ying, See-Chen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luo, Kaifu</au><au>Huopaniemi, Ilkka</au><au>Ala-Nissila, Tapio</au><au>Ying, See-Chen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymer translocation through a nanopore under an applied external field</atitle><jtitle>The Journal of chemical physics</jtitle><addtitle>J Chem Phys</addtitle><date>2006-03-21</date><risdate>2006</risdate><volume>124</volume><issue>11</issue><spage>114704</spage><epage>114704-7</epage><pages>114704-114704-7</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><coden>JCPSA6</coden><abstract>We investigate the dynamics of polymer translocation through a nanopore under an externally applied field using the two-dimensional fluctuating bond model with single-segment Monte Carlo moves. We concentrate on the influence of the field strength
E
, length of the chain
N
, and length of the pore
L
on forced translocation. As our main result, we find a crossover scaling for the translocation time
τ
with the chain length from
τ
∼
N
2
ν
for relatively short polymers to
τ
∼
N
1
+
ν
for longer chains, where
ν
is the Flory exponent. We demonstrate that this crossover is due to the change in the dependence of the translocation velocity
v
on the chain length. For relatively short chains
v
∼
N
−
ν
, which crosses over to
v
∼
N
−
1
for long polymers. The reason for this is that with increasing
N
there is a high density of segments near the exit of the pore, which slows down the translocation process due to slow relaxation of the chain. For the case of a long nanopore for which
R
||
, the radius of gyration
R
g
along the pore, is smaller than the pore length, we find no clear scaling of the translocation time with the chain length. For large
N
, however, the asymptotic scaling
τ
∼
N
1
+
ν
is recovered. In this regime,
τ
is almost independent of
L
. We have previously found that for a polymer, which is initially placed in the middle of the pore, there is a minimum in the escape time for
R
||
≈
L
. We show here that this minimum persists for weak fields
E
such that
E
L
is less than some critical value, but vanishes for large values of
E
L
.</abstract><cop>United States</cop><pub>American Institute of Physics</pub><pmid>16555907</pmid><doi>10.1063/1.2179792</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list); American Institute of Physics |
subjects | Electromagnetic Fields Models, Chemical Nanostructures - chemistry Nucleic Acids - chemistry Polymers - chemistry Proteins - chemistry |
title | Polymer translocation through a nanopore under an applied external field |
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