Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3215
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dc.contributor.authorSarabadani, Jalalen_US
dc.contributor.authorGHOSH, BAPPAen_US
dc.contributor.authorCHAUDHURY, SRABANTIen_US
dc.contributor.authorAla-Nissila, Tapioen_US
dc.date.accessioned2019-07-01T05:33:18Z
dc.date.available2019-07-01T05:33:18Z
dc.date.issued2018-01en_US
dc.identifier.citationEPL, 120(3), 38004.en_US
dc.identifier.issn0295-5075en_US
dc.identifier.issn1286-4854en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3215
dc.identifier.urihttps://doi.org/10.1209/0295-5075/120/38004en_US
dc.description.abstractWe consider the translocation dynamics of a polymer chain forced through a nanopore by an external force on its head monomer on the trans side. For a proper theoretical treatment we generalize the iso-flux tension propagation (IFTP) theory to include friction arising from the trans side subchain. The theory reveals a complicated scenario of multiple scaling regimes depending on the configurations of the cis and the trans side subchains. In the limit of high driving forces f such that the trans subchain is strongly stretched, the theory is in excellent agreement with molecular dynamics simulations and allows an exact analytic solution for the scaling of the translocation time ? as a function of the chain length N 0 and f. In this regime the asymptotic scaling exponents for ${\tau} \sim N_0^{\alpha} f^{\beta}$ are $\alpha=2$ , and $\beta =-1$ . The theory reveals significant correction-to-scaling terms arising from the cis side subchain and pore friction, which lead to a very slow approach to $\alpha =2$ from below as a function of increasing N 0.en_US
dc.language.isoenen_US
dc.publisherIOP Publishingen_US
dc.subjectDynamics of end-pulleden_US
dc.subjectPolymer translocationen_US
dc.subjectNanoporeen_US
dc.subjectDynamics of polymer translocationen_US
dc.subject2018en_US
dc.titleDynamics of end-pulled polymer translocation through a nanoporeen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleEPLen_US
dc.publication.originofpublisherForeignen_US
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