Nanosystem Research Institute, National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki 305-8562, Japan.
Langmuir. 2012 Feb 28;28(8):3887-95. doi: 10.1021/la204717c. Epub 2012 Feb 13.
Nanoparticles taken into biological systems can have biological impacts through their interactions with cell membranes, accompanied by protein adsorption onto the nanoparticle surfaces, forming a so-called protein corona. Our current research aims to demonstrate that nanoscale protein aggregates behave like such nanoparticles with regard to the interaction with lipid membranes. In this study, the adsorption and disruption of the lipid membranes by protein aggregates were investigated using amyloid fibrils and nanoscale thermal aggregates of lysozyme. Both types of protein aggregates had disruptive effects on the negatively charged liposomes, similar to polycationic nanoparticles. Interestingly, adsorption of liposomes on the amyloid fibrils preceding disruption occurred even if the net charge of the liposome was zero, suggesting the importance of hydrophobic interactions in addition to electrostatic interactions. The results of the present study provide new insights into the biological impacts of nanoparticles in vivo.
纳米颗粒进入生物系统后,可以通过与细胞膜的相互作用产生生物影响,同时蛋白质会吸附在纳米颗粒表面,形成所谓的蛋白质冠。我们目前的研究旨在证明纳米级蛋白质聚集体在与脂质膜相互作用方面的行为类似于这些纳米颗粒。在这项研究中,使用淀粉样纤维和溶菌酶的纳米级热聚集体研究了蛋白质聚集体对脂质膜的吸附和破坏。这两种类型的蛋白质聚集体对带负电荷的脂质体都有破坏作用,类似于阳离子纳米颗粒。有趣的是,即使脂质体的净电荷为零,脂质体在破坏前吸附在淀粉样纤维上的现象也会发生,这表明除了静电相互作用外,疏水性相互作用也很重要。本研究的结果为体内纳米颗粒的生物影响提供了新的见解。