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磷脂酰乙醇胺对抗菌肽 PGLa 诱导的孔形成的影响。

Effect of Phosphatidylethanolamine on Pore Formation Induced by the Antimicrobial Peptide PGLa.

机构信息

Integrated Bioscience Section, Graduate School of Science and Technology, Shizuoka University, Shizuoka 422-8529, Japan.

Nanomaterials Research Division, Research Institute of Electronics, Shizuoka University, Shizuoka 422-8529, Japan.

出版信息

J Phys Chem B. 2024 Mar 21;128(11):2684-2696. doi: 10.1021/acs.jpcb.3c08098. Epub 2024 Mar 7.

DOI:10.1021/acs.jpcb.3c08098
PMID:38450565
Abstract

Most antimicrobial peptides (AMPs) induce pore formation and a burst of lipid bilayers and plasma membranes. This causes severe leakage of the internal contents and cell death. The AMP PGLa forms nanopores in giant unilamellar vesicles (GUVs) comprising dioleoylphosphatidylcholine (DOPC) and dioleoylphosphatidylglycerol (DOPG). We here elucidated the effect of the line tension of a prepore rim on PGLa-induced nanopore formation by investigating the interaction of PGLa with single GUVs comprising dioleoylphosphatidylethanolamine (DOPE)/DOPG (6:4) in buffer using the single GUV method. We found that PGLa forms nanopores in the GUV membrane, which evolved into a local burst and burst of GUVs. The rate of pore formation in DOPE/DOPG-GUVs was smaller than that in DOPC/DOPG-GUVs. PGLa is located only in the outer leaflet of a GUV bilayer just before a fluorescent probe AF647 leakage from the inside, indicating that this asymmetric distribution induces nanopore formation. PGLa-induced local burst and burst of GUVs were observed at 10 ms-time resolution. After nanopore formation started, dense particles and small vesicles appeared in the GUVs, followed by a decrease in the GUV diameter. The GUV was finally converted into smaller GUV or lipid membrane aggregates. We discuss the mechanisms of PGLa-induced nanopore formation and its direct evolution to a GUV burst.

摘要

大多数抗菌肽 (AMPs) 诱导孔形成和脂质双层和质膜的爆裂。这会导致内部内容物的严重泄漏和细胞死亡。AMP PGLa 在由二油酰基磷脂酰胆碱 (DOPC) 和二油酰基磷脂酰甘油 (DOPG) 组成的巨大单层囊泡 (GUV) 中形成纳米孔。我们在这里通过使用单 GUV 方法研究 PGLa 与包含二油酰基磷脂酰乙醇胺 (DOPE)/DOPG(6:4) 的单个 GUV 相互作用,阐明了 prepore 边缘线张力对 PGLa 诱导的纳米孔形成的影响。我们发现 PGLa 在 GUV 膜中形成纳米孔,这些纳米孔演变成局部爆裂和 GUV 的爆裂。DOPE/DOPG-GUV 中的孔形成速率小于 DOPC/DOPG-GUV。PGLa 仅位于 GUV 双层的外叶,就在荧光探针 AF647 从内部泄漏之前,表明这种不对称分布诱导纳米孔形成。以 10ms 的时间分辨率观察到 PGLa 诱导的 GUV 局部爆裂和爆裂。在纳米孔形成开始后,在 GUV 中出现密集颗粒和小泡,随后 GUV 直径减小。GUV 最终转化为较小的 GUV 或脂质膜聚集体。我们讨论了 PGLa 诱导的纳米孔形成及其直接演变为 GUV 爆裂的机制。

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