Vineeth Kumar T V, Sanil George
Molecular Ecology Laboratory, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, Kerala. India.
Molecular Ecology Laboratory, Rajiv Gandhi Centre for Biotechnology, Thycaud P.O. Thiruvanathapuram- 695014. India.
Curr Protein Pept Sci. 2017;18(12):1263-1272. doi: 10.2174/1389203718666170710114932.
Research interests on amphibian antimicrobial peptides (AMPs) are currently increasing because of their capability to combat microorganisms from both terrestrial and aquatic environments, which are the warehouses of human pathogens. The most remarkable feature of AMPs are their mechanism of action, primarily targeted to anionic membranes. Researchers have postulated many models to describe peptide- membrane interaction, which leads to membrane permeation/intracellular targeting. Despite these models information regarding the relationship between membrane curvature and peptidemembrane interaction is scarce. This relationship could be clearly depicted using the two-state model and interfacial activity model. In the review, we discuss in detail the two state and interfacial activity models and explain the influence of membrane curvature on peptide binding and the membrane interaction of curvature-sensitive peptides. In addition, the models proposed to explain the mechanism of action of membrane lytic and non-lytic AMPs are also reviewed.
由于两栖类抗菌肽(AMPs)能够对抗来自陆地和水生环境中的微生物(而这些环境是人类病原体的储存库),目前对其的研究兴趣正在增加。AMPs最显著的特征是其作用机制,主要针对阴离子膜。研究人员提出了许多模型来描述肽与膜的相互作用,这种相互作用会导致膜渗透/细胞内靶向。尽管有这些模型,但关于膜曲率与肽-膜相互作用之间关系的信息却很少。使用双态模型和界面活性模型可以清楚地描述这种关系。在这篇综述中,我们详细讨论了双态模型和界面活性模型,并解释了膜曲率对肽结合以及曲率敏感肽的膜相互作用的影响。此外,还综述了为解释膜溶解型和非溶解型AMPs作用机制而提出的模型。