Jeong Hyun Seok, Kang Sunwoo, Lee Jin Yong, Kim Byeang Hyean
Department of Chemistry, BK School of Molecular Science, Pohang 790-784, Korea.
Org Biomol Chem. 2009 Mar 7;7(5):921-5. doi: 10.1039/b816768k. Epub 2009 Jan 23.
Recently, RNA bulges, three-dimensional structural motifs that function as molecular handles in RNA, were identified in various sequences and have been proposed as the interaction site for RNA-binding drugs. However direct and sensitive monitoring methods specific to RNA bulges have not been well developed. We describe here pyrene-labeled uridine derivatives which were incorporated into HIV TAR RNA bulge sites resulting in greatly enhanced fluorescence, allowing the effective monitoring of base conformations in HIV TAR RNA. To clarify this fluorescence enhancement, Hartree-Fock calculations were performed for natural and pyrene-labeled HIV TAR RNA. The calculated results showed a considerable rotation of the pyrene moiety at U25 due to argininamide-induced conformational changes in the RNA bulge. This simple and efficient method can be used to elucidate conformational changes in specific bulge regions.
最近,RNA凸起作为RNA中的分子柄发挥作用的三维结构基序,在各种序列中被鉴定出来,并被提议作为RNA结合药物的相互作用位点。然而,针对RNA凸起的直接且灵敏的监测方法尚未得到很好的发展。我们在此描述了芘标记的尿苷衍生物,其被掺入HIV TAR RNA凸起位点,导致荧光大大增强,从而能够有效监测HIV TAR RNA中的碱基构象。为了阐明这种荧光增强现象,对天然的和芘标记的HIV TAR RNA进行了哈特里-福克计算。计算结果表明,由于精氨酰胺诱导的RNA凸起构象变化,芘部分在U25处发生了相当大的旋转。这种简单而有效的方法可用于阐明特定凸起区域的构象变化。