Oligonucleotide Analogues with Integrated Bases and Backbone. Part 17
作者:Anne Ritter、Daniel Egli、Bruno Bernet、Andrea Vasella
DOI:10.1002/hlca.200890071
日期:2008.4
The formation of cyclic duplexes (pairing) of known oxymethylene-linked self-complementary U*[o]A(*) dinucleosides contrasts with the absence of pairing of the ethylene-linked U*[ca]A(*) analogues. The origin of this difference, and the expected association of U*[x]A(*) and A*[x]U(*) dinucleosides with x=CH2, O, or S was analysed. According to this analysis, pairing occurs via constitutionally isomeric
已知甲醛联自身互补U *的环状双链(配对)的形成[O]甲( * )二核苷对比与不存在乙烯联U *的配对的并[c一一种( * )的类似物。分析了这种差异的起源,以及预期的U * [x] A ( * )和A * [x] U ( * )双核苷与x = CH 2,O或S的缔合。根据此分析,配对通过结构异构的Watson–Crick,反向Watson – Crick,Hoogsteen或反向发生Hoogsteen H键合线性双工。它们中的每一个可以产生三个非对映异构的环状双链体,并且它们中的每个可以采用三个主要的构象。分析了x = CH 2,O或S的所有构象异构体的相对稳定性。具有x = CH 2的U * [x] A ( * )二核苷不会形成稳定的环状双链体,具有x = O的二核苷可能会形成具有关于C(4')C(5')键的gg构象的环状双链体, x = S的二核苷可以形成关于该键具有gt-构象的环状双链体。