Xu Yan, Ikeda Reiko, Sugiyama Hiroshi
Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University, Chiyoda, Tokyo 101-0062, Japan.
J Am Chem Soc. 2003 Nov 5;125(44):13519-24. doi: 10.1021/ja036233i.
Various modified guanine derivatives were synthesized and introduced into G(4) of d(CGCGCG)(2) to evaluate their capacity to stabilize Z-form DNA. It was found that the incorporation of 8-methylguanosine (m(8)rG) in oligonucleotides stabilizes the Z form more dramatically than does the incorporation of 8-methyl-2'-deoxyguanosine (m(8)G). This enhancement is ascribed to a reduction in the entropic penalty, which arises from the introduction of hydrophilic groups in solvent-exposed regions. The incorporation of m(8)rG into DNA sequences markedly stabilizes the Z form even in the absence of NaCl. The Z-DNA stabilizer allows oligonucleotides with a wide range of sequences to be converted to the Z form. It could be a powerful tool for examining the molecular basis of many types of Z-form-specific reactions at the molecular level under physiological salt conditions.
合成了各种修饰的鸟嘌呤衍生物,并将其引入到d(CGCGCG)(2)的G(4)中,以评估它们稳定Z型DNA的能力。研究发现,在寡核苷酸中掺入8-甲基鸟苷(m(8)rG)比掺入8-甲基-2'-脱氧鸟苷(m(8)G)更能显著稳定Z型。这种增强归因于熵罚的降低,这是由在溶剂暴露区域引入亲水基团引起的。即使在没有NaCl的情况下,将m(8)rG掺入DNA序列中也能显著稳定Z型。Z-DNA稳定剂能使具有广泛序列的寡核苷酸转化为Z型。它可能是在生理盐条件下在分子水平上研究许多类型Z型特异性反应的分子基础的有力工具。