Department of Chemistry , University of Basel , Mattenstrasse 24a, BPR 1096 , 4058 Basel , Switzerland.
BioEM Lab, Biozentrum , University of Basel , Mattenstrasse 26 , 4058 Basel , Switzerland.
Biomacromolecules. 2020 Feb 10;21(2):701-715. doi: 10.1021/acs.biomac.9b01416. Epub 2020 Jan 8.
Pore-forming peptides are of high biological relevance particularly as cytotoxic agents, but their properties are also applicable for the permeabilization of lipid membranes for biotechnological applications, which can then be translated to the more stable and versatile polymeric membranes. However, their interactions with synthetic membranes leading to pore formation are still poorly understood, hampering the development of peptide-based nanotechnological applications, such as biosensors or catalytic compartments. To elucidate these interactions, we chose the model peptide melittin, the main component of bee venom. Here, we present our systematic investigation on how melittin interacts with and inserts into synthetic membranes, based on amphiphilic block copolymers, to induce pore formation in three different setups (planar membranes and micrometric and nanometric vesicles). By varying selected molecular properties of block copolymers and resulting membranes (e.g., hydrophilic to hydrophobic block ratio, membrane thickness, surface roughness, and membrane curvature) and the stage of melittin addition to the synthetic membranes, we gained a deeper understanding of melittin insertion requirements. In the case of solid-supported planar membranes, melittin interaction was favored by membrane roughness and thickness, but its insertion and pore formation were hindered when the membrane was excessively thick. The additional property provided by micrometric vesicles, curvature, increased the functional insertion of melittin, which was evidenced by the even more curved nanometric vesicles. Using nanometric vesicles allowed us to estimate the pore size and density, and by changing the stage of melittin addition, we overcame the limitations of peptide-polymer membrane interaction. Mirroring the functionality assay of planar membranes, we produced glucose-sensing vesicles. The design of synthetic membranes permeabilized with melittin opens a new path toward the development of biosensors and catalytic compartments based on pore-forming peptides functionally inserted in synthetic planar or three-dimensional membranes.
孔形成肽具有很高的生物学相关性,特别是作为细胞毒性剂,但它们的性质也适用于生物技术应用中脂质膜的通透性,然后可以转化为更稳定和通用的聚合物膜。然而,它们与导致孔形成的合成膜的相互作用仍然知之甚少,这阻碍了基于肽的纳米技术应用的发展,例如生物传感器或催化隔室。为了阐明这些相互作用,我们选择了模型肽蜂毒素,它是蜜蜂毒液的主要成分。在这里,我们展示了我们对蜂毒素如何与合成膜相互作用并插入合成膜的系统研究,基于两亲性嵌段共聚物,以在三种不同设置(平面膜和微米和纳米囊泡)中诱导孔形成。通过改变嵌段共聚物和所得膜的选定分子性质(例如,亲水性到疏水性嵌段比、膜厚度、表面粗糙度和膜曲率)以及向合成膜添加蜂毒素的阶段,我们对蜂毒素插入的要求有了更深入的了解。在固支平面膜的情况下,膜粗糙度和厚度有利于蜂毒素的相互作用,但当膜过厚时,其插入和孔形成受到阻碍。微米囊泡提供的额外特性,曲率,增加了蜂毒素的功能插入,这一点通过甚至更弯曲的纳米囊泡得到了证明。使用纳米囊泡使我们能够估计孔径和密度,并且通过改变蜂毒素添加的阶段,我们克服了肽-聚合物膜相互作用的限制。我们模仿平面膜的功能测定,制作了葡萄糖感应囊泡。用蜂毒素通透性合成膜的设计为基于功能插入合成平面或三维膜的孔形成肽的生物传感器和催化隔室的开发开辟了新途径。