Institute of Organic Chemistry and Center for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, Innrain 80/82, 6020, Innsbruck, Austria.
Bachem Americas, Inc., 3132 Kashiwa Street, Torrance, CA 90505, USA.
Angew Chem Int Ed Engl. 2016 Sep 19;55(39):12008-12. doi: 10.1002/anie.201605870. Epub 2016 Aug 17.
In this work an improved stable isotope labeling protocol for nucleic acids is introduced. The novel building blocks eliminate/minimize homonuclear (13) C and (1) H scalar couplings thus allowing proton relaxation dispersion (RD) experiments to report accurately on the chemical exchange of nucleic acids. Using site-specific (2) H and (13) C labeling, spin topologies are introduced into DNA and RNA that make (1) H relaxation dispersion experiments applicable in a straightforward manner. The novel RNA/DNA building blocks were successfully incorporated into two nucleic acids. The A-site RNA was previously shown to undergo a two site exchange process in the micro- to millisecond time regime. Using proton relaxation dispersion experiments the exchange parameters determined earlier could be recapitulated, thus validating the proposed approach. We further investigated the dynamics of the cTAR DNA, a DNA transcript that is involved in the viral replication cycle of HIV-1. Again, an exchange process could be characterized and quantified. This shows the general applicablility of the novel labeling scheme for (1) H RD experiments of nucleic acids.
在这项工作中,我们引入了一种改进的稳定同位素标记核酸的方法。该新方法中的砌块可以消除/最小化同核 (13) C 和 (1) H 标量偶合,从而使质子弛豫分散 (RD) 实验能够准确地报告核酸的化学交换。通过对 DNA 和 RNA 的定点 (2) H 和 (13) C 标记,我们在 DNA 和 RNA 中引入了自旋拓扑结构,使得 (1) H 弛豫分散实验可以直接应用。新型 RNA/DNA 砌块已成功地被引入到两种核酸中。之前的研究表明,A 位 RNA 在微秒至毫秒的时间范围内经历双位点交换过程。使用质子弛豫分散实验,我们可以重现之前确定的交换参数,从而验证了所提出的方法。我们进一步研究了 cTAR DNA 的动力学,cTAR DNA 是一种参与 HIV-1 病毒复制周期的 DNA 转录本。同样,我们可以对其交换过程进行表征和定量。这表明,该新型标记方案可广泛应用于核酸的 (1) H RD 实验。