Huang Wei, Emani Prashant S, Varani Gabriele, Drobny Gary P
Department of Chemistry, University of Washington , Box 351700, Seattle 98195, United States.
J Phys Chem B. 2017 Jan 12;121(1):110-117. doi: 10.1021/acs.jpcb.6b11041. Epub 2016 Dec 21.
Intrinsic motions may allow HIV-1 transactivation response (TAR) RNA to change its conformation to form a functional complex with the Tat protein, which is essential for viral replication. Understanding the dynamic properties of TAR necessitates determining motion on the intermediate nanosecond-to-microsecond time scale. To this end, we performed solid-state deuterium NMR line-shape and T relaxation-time experiments to measure intermediate motions for two uridine residues, U40 and U42, within the lower helix of TAR. We infer global motions at rates of ∼10 s in the lower helix, which are much slower than those in the upper helix (∼10 s), indicating that the two helical domains reorient independently of one another in the solid-state sample. These results contribute to the aim of fully describing the properties of functional motions in TAR RNA.
内在运动可能使HIV-1反式激活应答(TAR)RNA改变其构象,以形成与Tat蛋白的功能复合物,这对病毒复制至关重要。了解TAR的动态特性需要确定纳秒至微秒中间时间尺度上的运动。为此,我们进行了固态氘核磁共振线形和T弛豫时间实验,以测量TAR下螺旋内两个尿苷残基U40和U42的中间运动。我们推断下螺旋中全局运动的速率约为10 s,这比上螺旋中的速率(约10 s)慢得多,表明在固态样品中两个螺旋结构域彼此独立地重新定向。这些结果有助于实现全面描述TAR RNA中功能运动特性的目标。