He Su-Zhen, Merlitz Holger, Sommer Jens-Uwe, Wu Chen-Xu
School of Mechanical and Electrical Engineering, Putian University, 351100, Putian, P.R. China.
Department of Physics and ITPA, Xiamen University, 361005, Xiamen, P.R. China.
Eur Phys J E Soft Matter. 2015 Sep;38(9):101. doi: 10.1140/epje/i2015-15101-9. Epub 2015 Sep 21.
We present molecular dynamics simulations of the interaction of fullerene-like, inhomogeneously charged proteins with polyelectrolyte brushes. A motivation of this work is the experimental observation that proteins, carrying an integral charge, may enter like-charged polymer brushes. Simulations of varying charge distributions on the protein surfaces are performed to unravel the physical mechanism of the adsorption. Our results prove that an overall neutral protein can be strongly driven into polyelectrolyte brush whenever the protein features patches of positive and negative charge. The findings reported here give further evidence that the strong adsorption of proteins is also driven by entropic forces due to counterion release, since charged patches on the surface of the proteins can act as multivalent counterions of the oppositely charged polyelectrolyte chains. A corresponding number of mobile co- and counterions is released from the brush and the vicinity of the proteins so that the entropy of the total system increases.
我们展示了类富勒烯的、电荷分布不均匀的蛋白质与聚电解质刷相互作用的分子动力学模拟。这项工作的一个动机是实验观察到,携带整数电荷的蛋白质可能会进入带相同电荷的聚合物刷。对蛋白质表面不同电荷分布进行模拟,以揭示吸附的物理机制。我们的结果证明,只要蛋白质具有正电荷和负电荷斑块,总体呈中性的蛋白质就能被强烈地驱动进入聚电解质刷。此处报道的研究结果进一步证明,蛋白质的强吸附也是由反离子释放引起的熵力驱动的,因为蛋白质表面的带电斑块可以作为带相反电荷的聚电解质链的多价反离子。相应数量的可移动共离子和反离子从刷以及蛋白质附近释放出来,从而使整个系统的熵增加。