Rohr Katja, Vogel Stefan
Nucleic Acid Center, Department of Chemistry, University of Southern Denmark, Campusvej 55, 5230 Odense, Denmark.
Chembiochem. 2006 Mar;7(3):463-70. doi: 10.1002/cbic.200500392.
The synthesis of amphiphilic polyaza crown ether monomers X (benzyl-substituted), Y (palmityl-substituted) and Z (cholesteryl-substituted) and their incorporation into oligonucleotides are described. Their effects on thermal duplex stability were investigated by UV melting curve analysis in different alkaline metal buffer solutions. Thermal-denaturation experiments showed remarkable stabilization of dsDNA by polyaza crown ether monomers when incorporated in opposite positions. The series of polyaza crown ether monomers (X, Y and Z) with different overall lipophilicities showed a trend of increased stability of the corresponding dsDNA with increasing lipophilicity of the polyaza crown ether monomer. Multiple incorporations of benzyl-substituted polyaza crown ether monomer X as dangling ends on both sides of dsDNA resulted in strongly increased stability of the corresponding duplex.
本文描述了两亲性聚氮杂冠醚单体X(苄基取代)、Y(棕榈酰基取代)和Z(胆固醇基取代)的合成及其与寡核苷酸的结合。通过在不同碱金属缓冲溶液中进行紫外熔解曲线分析,研究了它们对热双链稳定性的影响。热变性实验表明,当聚氮杂冠醚单体以相反位置掺入时,双链DNA会显著稳定。一系列具有不同整体亲脂性的聚氮杂冠醚单体(X、Y和Z)显示出,随着聚氮杂冠醚单体亲脂性的增加,相应双链DNA的稳定性呈增加趋势。将苄基取代的聚氮杂冠醚单体X作为双链DNA两侧的悬垂端进行多次掺入,导致相应双链体的稳定性大幅提高。