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Effects of chain flexibility on the conformational behavior of a single polymer chain
Effects of chain flexibility on conformational behavior as a function of temperature have been investigated by coarse-grained molecular dynamics (MD) simulation. The paper presents simulation results regarding the potential energies and structural parameters of a single polymer chain made of 100, 20...
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Published in: | Journal of polymer research 2015-12, Vol.22 (12), p.1-9, Article 236 |
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creator | Jiang, Zhouting Dou, Wenhui Sun, Tingting Shen, Yu Cao, Dan |
description | Effects of chain flexibility on conformational behavior as a function of temperature have been investigated by coarse-grained molecular dynamics (MD) simulation. The paper presents simulation results regarding the potential energies and structural parameters of a single polymer chain made of 100, 200, or 300 beads with various chain flexibilities. Our simulations exhibit the conformational transition from a random coil to a folded structure demonstrated by the curves of non-bonded potential energy, bond-orientational order parameters and characteristic ratios of real polymer chains with a cooling temperature. In this paper, the comparison between the real polymer chain model involving non-bonded interaction and the ideal polymer chain model in the absence of long-range interaction has also been made. It shows that the main factor inducing structural transition lies in the non-bonded interaction. This result explains clearly that the long-range interaction plays an important role in the polymer folding process. Moreover, the flexibility, as well as the chain length of a real polymer chain, strongly effects on its transition temperature. It also concludes that the changes of bond-torsional potential energy and characteristic ratio with the reduced temperature in the ideal polymer models are independent of chain length, but present different tendencies according to the chain flexibility. |
doi_str_mv | 10.1007/s10965-015-0875-3 |
format | article |
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The paper presents simulation results regarding the potential energies and structural parameters of a single polymer chain made of 100, 200, or 300 beads with various chain flexibilities. Our simulations exhibit the conformational transition from a random coil to a folded structure demonstrated by the curves of non-bonded potential energy, bond-orientational order parameters and characteristic ratios of real polymer chains with a cooling temperature. In this paper, the comparison between the real polymer chain model involving non-bonded interaction and the ideal polymer chain model in the absence of long-range interaction has also been made. It shows that the main factor inducing structural transition lies in the non-bonded interaction. This result explains clearly that the long-range interaction plays an important role in the polymer folding process. Moreover, the flexibility, as well as the chain length of a real polymer chain, strongly effects on its transition temperature. It also concludes that the changes of bond-torsional potential energy and characteristic ratio with the reduced temperature in the ideal polymer models are independent of chain length, but present different tendencies according to the chain flexibility.</description><identifier>ISSN: 1022-9760</identifier><identifier>EISSN: 1572-8935</identifier><identifier>DOI: 10.1007/s10965-015-0875-3</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Beads ; Bonding ; Chains (polymeric) ; Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Flexibility ; Industrial Chemistry/Chemical Engineering ; Mathematical models ; Molecular conformation ; Original Paper ; Polymer Sciences ; Potential energy ; Simulation</subject><ispartof>Journal of polymer research, 2015-12, Vol.22 (12), p.1-9, Article 236</ispartof><rights>Springer Science+Business Media Dordrecht 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c349t-c17ac68af51d965e09dc9c70495e67754804e9ff2edafabb46819c5d7223f1b23</citedby><cites>FETCH-LOGICAL-c349t-c17ac68af51d965e09dc9c70495e67754804e9ff2edafabb46819c5d7223f1b23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Jiang, Zhouting</creatorcontrib><creatorcontrib>Dou, Wenhui</creatorcontrib><creatorcontrib>Sun, Tingting</creatorcontrib><creatorcontrib>Shen, Yu</creatorcontrib><creatorcontrib>Cao, Dan</creatorcontrib><title>Effects of chain flexibility on the conformational behavior of a single polymer chain</title><title>Journal of polymer research</title><addtitle>J Polym Res</addtitle><description>Effects of chain flexibility on conformational behavior as a function of temperature have been investigated by coarse-grained molecular dynamics (MD) simulation. 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It also concludes that the changes of bond-torsional potential energy and characteristic ratio with the reduced temperature in the ideal polymer models are independent of chain length, but present different tendencies according to the chain flexibility.</description><subject>Beads</subject><subject>Bonding</subject><subject>Chains (polymeric)</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Flexibility</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Mathematical models</subject><subject>Molecular conformation</subject><subject>Original Paper</subject><subject>Polymer Sciences</subject><subject>Potential energy</subject><subject>Simulation</subject><issn>1022-9760</issn><issn>1572-8935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp1kE9LwzAYh4MoOKcfwFvAi5dqkiZNc5ThPxh4ceeQpm-2jLaZSSfu25tRDyJIeMl7eH4_kgeha0ruKCHyPlGiKlEQmqeWoihP0IwKyYpaleI074SxQsmKnKOLlLaECCGreoZWj86BHRMODtuN8QN2HXz5xnd-POAw4HED2IbBhdib0YfBdLiBjfn0IR4zBic_rDvAu9AdeohTySU6c6ZLcPVzz9Hq6fF98VIs355fFw_LwpZcjYWl0tiqNk7QNr8eiGqtspJwJaCSUvCacFDOMWiNM03Dq5oqK1rJWOlow8o5up16dzF87CGNuvfJQteZAcI-aVqTfBSXPKM3f9Bt2Mf8nUxJrqrsTx4L6UTZGFKK4PQu-t7Eg6ZEH0XrSbTOovVRtC5zhk2ZlNlhDfFX87-hb8ikgFs</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Jiang, Zhouting</creator><creator>Dou, Wenhui</creator><creator>Sun, Tingting</creator><creator>Shen, Yu</creator><creator>Cao, Dan</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20151201</creationdate><title>Effects of chain flexibility on the conformational behavior of a single polymer chain</title><author>Jiang, Zhouting ; 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The paper presents simulation results regarding the potential energies and structural parameters of a single polymer chain made of 100, 200, or 300 beads with various chain flexibilities. Our simulations exhibit the conformational transition from a random coil to a folded structure demonstrated by the curves of non-bonded potential energy, bond-orientational order parameters and characteristic ratios of real polymer chains with a cooling temperature. In this paper, the comparison between the real polymer chain model involving non-bonded interaction and the ideal polymer chain model in the absence of long-range interaction has also been made. It shows that the main factor inducing structural transition lies in the non-bonded interaction. This result explains clearly that the long-range interaction plays an important role in the polymer folding process. Moreover, the flexibility, as well as the chain length of a real polymer chain, strongly effects on its transition temperature. It also concludes that the changes of bond-torsional potential energy and characteristic ratio with the reduced temperature in the ideal polymer models are independent of chain length, but present different tendencies according to the chain flexibility.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10965-015-0875-3</doi><tpages>9</tpages></addata></record> |
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subjects | Beads Bonding Chains (polymeric) Characterization and Evaluation of Materials Chemistry Chemistry and Materials Science Flexibility Industrial Chemistry/Chemical Engineering Mathematical models Molecular conformation Original Paper Polymer Sciences Potential energy Simulation |
title | Effects of chain flexibility on the conformational behavior of a single polymer chain |
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