Department of Chemistry, Institute for Biophysical Dynamics and James Franck Institute, University of Chicago, Illinois 60637, USA.
Biomacromolecules. 2012 Sep 10;13(9):2616-23. doi: 10.1021/bm300847x. Epub 2012 Aug 3.
PEO-PPO-PEO triblock copolymers have opposing effects on lipid membrane integrity: they can behave either as membrane sealants or as membrane permeabilizers. To gain insights into their biomembrane activities, the fundamental interactions between a series of PEO-based polymers and phospholipid vesicles were investigated. Specifically, the effect of copolymer hydrophobicity on its ability to prevent liposomes from peroxidation was evaluated, and partitioning free energy and coefficient involved in the interactions were derived. Our results show that the high degree of hydrophilicity is a key feature of the copolymers that can effectively protect liposomes from peroxidation and the protective effect of the copolymers stems from their adsorption at the membrane surface without penetrating into the bilayer core. The origin of this protective effect induced by polymer absorption is attributed to the retardation of membrane hydration dynamics, which is further illustrated in the accompanying study on dynamic nuclear polarization (DNP)-derived hydration dynamics (Cheng, C.-Y.; Wang, J.-Y.; Kausik, R.; Lee, K. Y. C.; Han S. Biomacromolecules, 2012, DOI: 10.1021/bm300848c).
PEO-PPO-PEO 嵌段共聚物对脂膜完整性有相反的影响:它们可以作为膜密封剂或膜通透剂。为了深入了解它们在生物膜中的活性,研究了一系列基于 PEO 的聚合物与磷脂囊泡之间的基本相互作用。具体而言,评估了共聚物疏水性对其防止脂质体过氧化能力的影响,并推导了参与相互作用的自由能和系数。我们的结果表明,高亲水性是共聚物的关键特征,可有效保护脂质体免受过氧化,共聚物的保护作用源于其在膜表面的吸附,而不穿透双层核心。聚合物吸收引起这种保护作用的原因归因于膜水合动力学的延迟,这在伴随的基于动态核极化 (DNP) 的水合动力学研究中进一步说明了(Cheng, C.-Y.; Wang, J.-Y.; Kausik, R.; Lee, K. Y. C.; Han S. Biomacromolecules, 2012, DOI: 10.1021/bm300848c)。