Zhang Qi, Throolin Rachel, Pitt Stephen W, Serganov Alexander, Al-Hashimi Hashim M
Department of Chemistry and Biophysics Research Division, University of Michigan, Ann Arbor, MI 48109, USA.
J Am Chem Soc. 2003 Sep 3;125(35):10530-1. doi: 10.1021/ja0363056.
Approaches developed thus for extracting structural and dynamical information from RDCs have rested on the assumption that motions do not affect molecular alignment. However, it is well established that molecular alignment in ordered media is dependent on conformation, and slowly interconverting conformational substates may exhibit different alignment properties. Neglecting these correlation effects can lead to aberrations in the structural and dynamical analysis of RDCs and diminish the utility of RDCs in probing motions between domains having similar alignment propensities. Here, we introduce a new approach based on measurement of magnetic field induced residual dipolar couplings in nucleic acids which can explicitly take into account such correlations and demonstrate measurements of motions between two "magnetically equivalent" domains in the transactivation response element (TAR) RNA.
因此,为从残余偶极耦合(RDCs)中提取结构和动力学信息而开发的方法一直基于这样一种假设,即分子运动不会影响分子排列。然而,众所周知,有序介质中的分子排列取决于构象,并且缓慢相互转化的构象亚态可能表现出不同的排列特性。忽略这些相关效应会导致RDCs结构和动力学分析中的偏差,并降低RDCs在探测具有相似排列倾向的结构域之间运动时的效用。在这里,我们引入了一种基于测量核酸中磁场诱导的残余偶极耦合的新方法,该方法可以明确考虑此类相关性,并展示了对反式激活应答元件(TAR)RNA中两个“磁等价”结构域之间运动的测量。