信使核糖核酸
合理设计
纳米颗粒
计算生物学
化学
纳米技术
细胞生物学
计算机科学
生物
材料科学
生物化学
基因
作者
Seo‐Hyeon Bae,Hosam Choi,Jisun Lee,Min‐Ho Kang,Seong‐Ho Ahn,Yu‐Sun Lee,Huijeong Choi,Sohee Jo,Yeeun Lee,Hyo‐Jung Park,Seonghyun Lee,Subin Yoon,Gahyun Roh,Seongje Cho,Youngran Cho,Dahyeon Ha,Soo‐Yeon Lee,Eun‐Jin Choi,Ayoung Oh,Jungmin Kim
出处
期刊:Small
[Wiley]
日期:2024-09-12
卷期号:21 (8): e2405618-e2405618
被引量:27
标识
DOI:10.1002/smll.202405618
摘要
Abstract Since the coronavirus pandemic, mRNA vaccines have revolutionized the field of vaccinology. Lipid nanoparticles (LNPs) are proposed to enhance mRNA delivery efficiency; however, their design is suboptimal. Here, a rational method for designing LNPs is explored, focusing on the ionizable lipid composition and structural optimization using machine learning (ML) techniques. A total of 213 LNPs are analyzed using random forest regression models trained with 314 features to predict the mRNA expression efficiency. The models, which predict mRNA expression levels post‐administration of intradermal injection in mice, identify phenol as the dominant substructure affecting mRNA encapsulation and expression. The specific phospholipids used as components of the LNPs, as well as the N/P ratio and mass ratio, are found to affect the efficacy of mRNA delivery. Structural analysis highlights the impact of the carbon chain length on the encapsulation efficiency and LNP stability. This integrated approach offers a framework for designing advanced LNPs and has the potential to unlock the full potential of mRNA therapeutics.
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