抗菌肽
化学
膜
膜透性
分子动力学
生物物理学
计算生物学
纳米技术
膜完整性
膜生物物理学
膜蛋白
功能多样性
小分子
脂质双层
结构完整性
药物发现
分子模型
细胞膜
生物化学
补语(音乐)
细胞生物学
作者
Sofia Cresca,Jure Borišek,Alessandra Magistrato,Igor Križaj
标识
DOI:10.1021/acs.jcim.5c02731
摘要
Biological membranes are crucial for cellular integrity and function, but their selective permeability can be compromised by various peptides and proteins, such as antimicrobial peptides (AMPs) and pore-forming proteins/toxins (PFPs/PFTs). These molecules induce membrane permeabilization through diverse mechanisms, ranging from the formation of well-defined pores to more nuanced disruptions of the lipid bilayer. Understanding molecular mechanisms underlying membrane integrity disruption is vital for developing novel tools to be applied in medicine, biotechnology, and agriculture. However, due to their transient and dynamic nature, characterizing membrane-disrupting mechanisms is a significant experimental challenge. In silico methods, particularly all-atom and coarse-grained molecular dynamics (MD) simulations, are an indispensable tool to complement and enrich experimental studies, and can offer detailed insights into peptide/protein–membrane interactions, insertion, oligomerization, and pore formation. This review provides a comprehensive overview of the structural and mechanistic diversity of AMPs and PFPs, highlighting representative case studies and discussing key challenges emerging from MD simulations.
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