Confined crowded polymers near attractive surfaces

被引:4
|
作者
Tripathi, Kamal [1 ,2 ]
Menon, Gautam I. [1 ,2 ,3 ]
Vemparala, Satyavani [1 ,2 ]
机构
[1] Inst Math Sci, CIT Campus, Chennai 600113, Tamil Nadu, India
[2] Homi Bhabha Natl Inst, Training Sch Complex, Mumbai 400094, Maharashtra, India
[3] Ashoka Univ, Dept Phys, Plot 2, Natl Capital Region 131029, Sonepat, India
来源
JOURNAL OF CHEMICAL PHYSICS | 2019年 / 151卷 / 24期
关键词
SPATIAL-ORGANIZATION; CELLULAR ENVIRONMENTS; DEPLETION POTENTIALS; PROTEIN; MODELS; STABILITY; COSOLUTES; COLLAPSE; COATINGS; ENTROPY;
D O I
10.1063/1.5115284
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present results from molecular dynamics simulations of a spherically confined neutral polymer in the presence of crowding particles, studying polymer shapes and conformations as a function of the strength of the attraction to the confining wall, solvent quality, and the density of crowders. The conformations of the polymer under good solvent conditions are weakly dependent on crowder particle density, even when the polymer is strongly confined. In contrast, under poor solvent conditions, when the polymer assumes a collapsed conformation when unconfined, it can exhibit transitions to two different adsorbed phases, when either the interaction with the wall or the density of crowder particles is changed. One such transition involves a desorbed collapsed phase change to an adsorbed extended phase as the attraction of the polymer towards the confining wall is increased. Such an adsorbed extended phase can exhibit a second transition to an ordered adsorbed collapsed phase as the crowder particle density is increased. The ordered adsorbed collapsed phase of the polymer differs significantly in its structure from the desorbed collapsed phase. We revisit the earlier understanding of the adsorption of confined polymers on attractive surfaces in light of our results.
引用
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页数:10
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