Haley Jennifer, Kabiru Paul, Geng Yan
Department of Chemistry, University of Georgia, Athens, GA 30602, USA.
Mol Biosyst. 2010 Jan;6(1):249-55. doi: 10.1039/b908873c. Epub 2009 Sep 25.
DNA condensation in-vitro has been studied as a model system to reveal common principles underlying gene packaging in biology, and as the critical first step towards the development of non-viral gene delivery vectors. In this study, we use a bio-inspired approach, where small DNA-binding peptides are controllably clustered by an amphiphilic block copolymer scaffold, to reveal the effect of clustered peptide binding on the energetics, size, shape and physical properties of DNA condensation in-vitro. This provides insights into the general architectural effect of gene-binding proteins on DNA condensation process. Moreover, the versatility afforded by regulating the clustering density and composition of peptides may provide a novel design platform for gene delivery applications in the future.
体外DNA凝聚作为一种模型系统,已被用于揭示生物学中基因包装的共同原理,也是开发非病毒基因递送载体至关重要的第一步。在本研究中,我们采用了一种受生物启发的方法,即通过两亲性嵌段共聚物支架可控地聚集小DNA结合肽,以揭示聚集肽结合对体外DNA凝聚的能量学、大小、形状和物理性质的影响。这为深入了解基因结合蛋白对DNA凝聚过程的总体结构效应提供了思路。此外,通过调节肽的聚集密度和组成所提供的多功能性,可能为未来的基因递送应用提供一个新的设计平台。