两亲性
凝聚
核糖核酸
核酸
摩尔质量
聚合物
阳离子聚合
高分子
共聚物
化学
生物物理学
合理设计
寡核苷酸
纳米颗粒
胶束
基因传递
自组装
纳米技术
材料科学
动态光散射
肺表面活性物质
脂质双层
药物输送
小角中子散射
高分子化学
形态学(生物学)
化学工程
中子散射
组合化学
水溶液
纳米棒
聚电解质
膜
作者
Paul J. Hurst,Yuan Jia,Summer Ramsay-Burrough,Rebecca L. McClellan,Joshua T. Arens,Samuel R. Khasnavis,Trevor J. Del Castillo,Mahmoud M. AbdElwakil,Michael Lueckheide,Vivek M. Prabhu,Robert M. Waymouth
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-11-06
卷期号:19 (45): 38954-38969
标识
DOI:10.1021/acsnano.5c07147
摘要
Advances in nucleic acid delivery have inspired efforts to mimic the function of natural viruses through the development of self-assemblies capable of gene delivery. RNA assemblies based on amphiphilic polymers are emerging as alternatives to lipid nanoparticles, but the factors that govern the self-assembly of RNA with polymeric amphiphiles are poorly understood. Here, we describe the structure of coacervate nanoparticle assemblies derived from RNA and synthetic cationic polymer amphiphiles based on Charge Altering Releasable Transporters (CARTs). CARTs are effective gene delivery agents derived from block copolymer amphiphiles. Cryogenic electron microscopy and tomography (CryoEM, CryoET), small-angle neutron scattering (SANS) and small-angle X-ray scattering (SAXS) reveal that the self-assembly of RNA with low molar mass (≤10,000 g/mol) CART amphiphiles generates nanoparticles with disordered bicontinuous internal morphologies composed of interpenetrating lipid and aqueous coacervate domains. Systematic variation of the cationic and lipophilic blocks in low molar mass CART amphiphiles demonstrates that both the internal domain spacings (6 to 8 nm) and the order of the resulting bicontinuous CART-RNA assemblies depend on the CART chemical structure and the oligonucleotide cargo (mRNA vs siRNA). Notably, the presence of RNA drives the formation of bicontinuous morphologies. In contrast, CART/RNA assemblies with higher molar mass (≥28,000 g/mol) CART amphiphiles fail to generate bicontinuous assemblies, instead yielding aggregates composed of particles approximately 10 to 20 nm in diameter. This work illuminates the internal morphologies of RNA assemblies with synthetic block copolymer amphiphiles, with implications for the rational design of polymer-based RNA delivery systems.
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