内体
阳离子聚合
化学
基因传递
生物物理学
脂质双层融合
细胞生物学
融合
转染
动力学
小泡
亚稳态
膜
阳离子脂质体
内吞作用
基因转移
药物输送
体外
细胞
遗传增强
纳米颗粒
生物化学
基因表达
脂质体
细胞膜
体内
融合基因
作者
Anurag Sharma,Khushika Khushika,Monika Chaudhary,Pritam Kumar Jana,Nagma Parveen
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2025-12-05
卷期号:18 (3): 1420-1432
摘要
Lipid nanoparticles (LNPs) have gained significant attention because of the clinical success of the Onpattro drug and mRNA vaccines. Two major challenges remain: (i) designing LNPs for gene therapy targeting non-liver tissues and (ii) overcoming inefficient endosomal escape of conventional LNPs. Cationic LNPs have been reported to shift the organ tropism, but their endosomal escape is yet to be evaluated. Here, we investigated the fusion dynamics of cationic LNPs with model membranes at the single-particle level. We found that the membrane fusion occurs through a unique mass transfer pathway, involving a one-step transition that forms a metastable intermediate that fully coalesces with the target membrane. A moderately high concentration (31 mol%) of the cationic lipid (DOTAP), combined with either DOPE or DSPC + cholesterol helper lipids, accelerates the fusion kinetics by reducing the lag time. The enhanced fusogenicity of these compositions aligns with the bulk-phase lipid mixing results. Endosomal localization and eGFP expression upon gene delivery in a range of mammalian cell lines confirm effective endosomal escape of DOPE- or DSPC + cholesterol-rich cationic LNPs. Overall, these findings represent a step toward designing optimal cationic LNP candidates for efficient gene delivery to organs beyond the liver.
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