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Related Concept Videos

Actin Polymerization and Cell Motility01:13

Actin Polymerization and Cell Motility

Actin is a family of globular proteins that are highly abundant in eukaryotic cells. It makes up approximately 1-5% of total cell protein concentration. Actin monomers polymerize to form a complex network of polarized filaments, the actin cytoskeleton, that plays a crucial role in many cellular processes, including cell motility, division, endocytosis, and metastasis of cancer cells.
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Cotranslational Protein Translocation01:20

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Translocation of proteins across membranes is an ancient process that occurs even in bacteria and archaebacteria. In fact, the components of the translocation machinery are still conserved between prokaryotes and eukaryotes.
Sec61 channel partners for cotranslational translocation
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Related Experiment Video

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Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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Polymer translocation in a double-force arrangement.

S T T Ollila1, K F Luo, T Ala-Nissila

  • 1Department of Applied Physics, Helsinki University of Technology, P.O. Box 1100, FIN-02015 TKK, Espoo, Finland. santtu.ollila@tkk.fi

The European Physical Journal. E, Soft Matter
|March 28, 2009
PubMed
Summary

This study explores polymer translocation through nanopores using a double-force method for biopolymer sequencing. While slower, this method offers better control over polymer movement during translocation.

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Area of Science:

  • Biophysics
  • Polymer Physics
  • Nanotechnology

Background:

  • Polymer translocation through nanopores is crucial for biopolymer sequencing.
  • External forces are used to drive and control this process.
  • A double-force arrangement has been proposed for enhanced dynamical control.

Purpose of the Study:

  • To investigate the translocation dynamics of a driven polymer chain through a nanopore under a double-force arrangement.
  • To analyze the effect of opposing forces on translocation time and control.
  • To provide data for estimating sequencing errors in double-force experiments.

Main Methods:

  • Langevin dynamics simulations were employed.
  • A pulling force was applied to the first monomer.
  • An opposing force was applied within the pore.

Main Results:

  • Translocation is slower in the double-force arrangement compared to a single pulling force.
  • The scaling of translocation time with chain length (tau ~ N^2) remains unchanged.
  • Waiting times for monomer exit increase with bead number, indicating controlled velocity.

Conclusions:

  • The double-force arrangement allows for better dynamical control of polymer translocation.
  • This method shows promise for precise biopolymer sequencing.
  • Understanding translocation dynamics is key to minimizing sequencing errors.