Semiflexible Macromolecules In Quasi-One-Dimensional Confinement: Discrete Versus Continuous Bond Angles
Abstract
The conformations of semiflexible polymers in two dimensions confined in a strip of width D are studied by computer simulations, investigating two different models for the mechanism by which chain stiffness is realized. One model (studied by molecular dynamics) is a bead-spring model in the continuum, where stiffness is controlled by a bond angle potential allowing for arbitrary bond angles. The other model (studied by Monte Carlo) is a self-avoiding walk chain on the square lattice, where only discrete bond angles (0° and ±90°) are possible, and the bond angle potential then controls the density of kinks along the chain contour. The first model is a crude description of DNA-like biopolymers, while the second model (roughly) describes synthetic polymers like alkane chains. It is first demonstrated that in the bulk the crossover from rods to self-avoiding walks for both models is very similar, when one studies average chain linear dimensions, transverse fluctuations, etc., despite their differences in local conformations. However, in quasi-one-dimensional confinement two significant differences between both models occur: (i) The persistence length (extracted from the average cosine of the bond angle) gets renormalized for the lattice model when D gets less than the bulk persistence length, while in the continuum model it stays unchanged. (ii) The monomer density near the repulsive walls for semiflexible polymers is compatible with a power law predicted for the Kratky-Porod model in the case of the bead-spring model, while for the lattice case it tends to a nonzero constant across the strip. However, for the density of chain ends, such a constant behavior seems to occur for both models, unlike the power law observed for flexible polymers. In the regime where the bulk persistence length ℓp is comparable to D, hairpin conformations are detected, and the chain linear dimensions are discussed in terms of a crossover from the Daoud/De Gennes "string of blobs"-picture to the flexible rod picture when D decreases and/or the chain stiffness increases. Introducing a suitable further coarse-graining of the chain contours of the continuum model, direct estimates for the deflection length and its distribution could be obtained.
Publication Date
12-28-2015
Publication Title
Journal of Chemical Physics
Volume
143
Issue
24
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1063/1.4929600
Copyright Status
Unknown
Socpus ID
84940511073 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/84940511073
STARS Citation
Huang, Aiqun; Hsu, Hsiao Ping; Bhattacharya, Aniket; and Binder, Kurt, "Semiflexible Macromolecules In Quasi-One-Dimensional Confinement: Discrete Versus Continuous Bond Angles" (2015). Scopus Export 2015-2019. 46.
https://stars.library.ucf.edu/scopus2015/46