Liu Bo, Yu Peng, Alluri Prasanna G, Kodadek Thomas
Department of Internal Medicine and the Division for Translational Research, University of Texas Southwestern Medical Center, Dallas, TX 75390-8573, USA.
Mol Biosyst. 2005 Oct;1(4):307-17. doi: 10.1039/b511514k. Epub 2005 Sep 19.
Hairpin poly(amide)s (HPs) are sequence specific DNA-binding compounds that have engendered considerable interest as potential pharmacological agents to manipulate the expression of specific genes. However, recent reports have indicated that the ability of HP conjugates to pass through cell membranes is sensitive to the cell type employed and the nature of the conjugate. Furthermore, while binding of HPs to DNA sequences in vitro is relatively well understood, packing of DNA into chromatin in living cells makes predicting the efficiency with which a given poly(amide) will bind its cognate site less certain. Previous methods to evaluate HP permeability and binding in vivo, while effective, are somewhat tedious and qualitative. We report here two related reporter gene-based assays that provide a more convenient and quantitative measure of poly(amide) permeability and DNA binding activity in living cells. We anticipate that these methods will complement existing tools and facilitate the development of HP conjugates with the desired biological activity.
发夹型聚酰胺(HPs)是序列特异性DNA结合化合物,作为操纵特定基因表达的潜在药物制剂引起了广泛关注。然而,最近的报告表明,HP缀合物穿过细胞膜的能力对所使用的细胞类型和缀合物的性质敏感。此外,虽然HPs与体外DNA序列的结合相对容易理解,但在活细胞中将DNA包装成染色质使得预测给定聚酰胺与其同源位点结合的效率变得不太确定。以前评估HP体内通透性和结合的方法虽然有效,但有些繁琐且定性。我们在此报告两种基于报告基因的相关检测方法,它们能更方便、定量地测量活细胞中聚酰胺的通透性和DNA结合活性。我们预计这些方法将补充现有工具,并促进具有所需生物活性的HP缀合物的开发。