Végh Attila Gergely, Nagy Krisztina, Bálint Zoltán, Kerényi Adám, Rákhely Gábor, Váró György, Szegletes Zsolt
Institute of Biophysics, Biological Research Centre, Hungarian Academy of Sciences, P.O. Box 521, 6701 Szeged, Hungary.
J Biomed Biotechnol. 2011;2011:670589. doi: 10.1155/2011/670589. Epub 2011 Jun 22.
Indolicidin, a cationic antimicrobial tridecapeptide amide, is rich in proline and tryptophan residues. Its biological activity is intensively studied, but the details how indolicidin interacts with membranes are not fully understood yet. We report here an in situ atomic force microscopic study describing the effect of indolicidin on an artificial supported planar bilayer membrane of dipalmitoyl phosphatidylcholine (DPPC) and on purple membrane of Halobacterium salinarum. Concentration dependent interaction of the peptide and membranes was found in case of DPPC resulting the destruction of the membrane. Purple membrane was much more resistant against indolicidin, probably due to its high protein content. Indolicidin preferred the border of membrane disks, where the lipids are more accessible. These data suggest that the atomic force microscope is a powerful tool in the study of indolicidin-membrane interaction.
吲哚杀菌素是一种富含脯氨酸和色氨酸残基的阳离子抗菌十三肽酰胺。其生物活性已得到深入研究,但吲哚杀菌素与膜相互作用的具体细节尚未完全了解。我们在此报告一项原位原子力显微镜研究,描述了吲哚杀菌素对二棕榈酰磷脂酰胆碱(DPPC)人工支持平面双层膜以及盐生盐杆菌紫膜的影响。在DPPC的情况下,发现肽与膜的相互作用呈浓度依赖性,导致膜的破坏。紫膜对吲哚杀菌素的抗性更强,这可能是由于其蛋白质含量高。吲哚杀菌素更喜欢膜盘的边缘,那里的脂质更容易接近。这些数据表明,原子力显微镜是研究吲哚杀菌素与膜相互作用的有力工具。