Effects of molecular model, ionic strength, divalent ions, and hydrophobic interaction on human neurofilament conformation.

Autor: Lee, Joonseong, Kim, Seonghoon, Chang, Rakwoo, Jayanthi, Lakshmi, Gebremichael, Yeshitila
Předmět:
Zdroj: Journal of Chemical Physics; 1/7/2013, Vol. 138 Issue 1, p015103-015103-15, 1p, 4 Diagrams, 1 Chart, 8 Graphs
Abstrakt: The present study examines the effects of the model dependence, ionic strength, divalent ions, and hydrophobic interaction on the structural organization of the human neurofilament (NF) brush, using canonical ensemble Monte Carlo (MC) simulations of a coarse-grained model with the amino-acid resolution. The model simplifies the interactions between the NF core and the sidearm or between the sidearms by the sum of excluded volume, electrostatic, and hydrophobic interactions, where both monovalent salt ions and solvents are implicitly incorporated into the electrostatic interaction potential. Several important observations are made from the MC simulations of the coarse-grained model NF systems. First, the mean-field type description of monovalent salt ions works reasonably well in the NF system. Second, the manner by which the NF sidearms are arranged on the surface of the NF backbone core has little influence on the lateral extension of NF sidearms. Third, the lateral extension of the NF sidearms is highly affected by the ionic strength of the system: at low ionic strength, NF-M is most extended but at high ionic strength, NF-H is more stretched out because of the effective screening of the electrostatic interaction. Fourth, the presence of Ca2 + ions induces the attraction between negatively charged residues, which leads to the contraction of the overall NF extension. Finally, the introduction of hydrophobic interaction does not change the general structural organization of the NF sidearms except that the overall extension is contracted. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index