Laboratoire Structure et Activité des Biomolécules Normales et Pathologiques, Université d'Evry-Val-d'Essonne and INSERM U829, Evry, France.
Langmuir. 2010 Nov 16;26(22):17552-7. doi: 10.1021/la103066c. Epub 2010 Oct 7.
Introduction of nucleic acids into cells is an important biotechnology research field which also holds great promise for therapeutic applications. One of the key steps in the gene delivery process is compaction of DNA into nanometric particles. The study of DNA condensing properties of three linear cationic triblock copolymers poly(ethylenimine-b-propylene glycol-b-ethylenimine), namely, LPEI(50)-PPG(36)-LPEI(50), LPEI(19)-PPG(36)-LPEI(19), and LPEI(14)-PPG(68)-LPEI(14), indicates that proper DNA condensation is driven by both the charge and the size of the respective cationic hydrophilic linear polyethylenimine (LPEI) and neutral hydrophobic poly(propylene glycol) (PPG) parts. Atomic force microscopy was used to investigate the interactions of the triblock copolymers with plasmid DNA at the single molecule level and to enlighten the mechanism involved in DNA condensation.
核酸导入细胞是生物技术研究的重要领域,在治疗应用方面也具有巨大的潜力。基因传递过程中的关键步骤之一是将 DNA 压缩成纳米级颗粒。三种线性阳离子三嵌段共聚物聚(乙二胺-b-丙二醇-b-乙二胺),即 LPEI(50)-PPG(36)-LPEI(50)、LPEI(19)-PPG(36)-LPEI(19)和 LPEI(14)-PPG(68)-LPEI(14)的 DNA 凝聚特性研究表明,适当的 DNA 凝聚是由各自的阳离子亲水线性聚乙烯亚胺(LPEI)和中性疏水性聚(丙二醇)(PPG)部分的电荷和大小共同驱动的。原子力显微镜用于在单分子水平上研究三嵌段共聚物与质粒 DNA 的相互作用,并阐明 DNA 凝聚所涉及的机制。