Russell Rick, Zhuang Xiaowei, Babcock Hazen P, Millett Ian S, Doniach Sebastian, Chu Steven, Herschlag Daniel
Department of Biochemistry, Stanford University, Stanford, CA 94305, USA.
Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):155-60. doi: 10.1073/pnas.221593598. Epub 2001 Dec 26.
Structured RNAs achieve their active states by traversing complex, multidimensional energetic landscapes. Here we probe the folding landscape of the Tetrahymena ribozyme by using a powerful approach: the folding of single ribozyme molecules is followed beginning from distinct regions of the folding landscape. The experiments, combined with small-angle x-ray scattering results, show that the landscape contains discrete folding pathways. These pathways are separated by large free-energy barriers that prevent interconversion between them, indicating that the pathways lie in deep channels in the folding landscape. Chemical protection and mutagenesis experiments are then used to elucidate the structural features that determine which folding pathway is followed. Strikingly, a specific long-range tertiary contact can either help folding or hinder folding, depending on when it is formed during the process. Together these results provide an unprecedented view of the topology of an RNA folding landscape and the RNA structural features that underlie this multidimensional landscape.
结构化RNA通过穿越复杂的多维能量景观来达到其活性状态。在这里,我们使用一种强大的方法来探究嗜热四膜虫核酶的折叠景观:从折叠景观的不同区域开始追踪单个核酶分子的折叠过程。这些实验与小角X射线散射结果相结合,表明该景观包含离散的折叠途径。这些途径被巨大的自由能屏障隔开,阻止它们之间的相互转换,这表明这些途径位于折叠景观的深通道中。然后利用化学保护和诱变实验来阐明决定遵循哪种折叠途径的结构特征。令人惊讶的是,一种特定的长程三级接触根据其在过程中形成的时间不同,既可以帮助折叠,也可以阻碍折叠。这些结果共同提供了关于RNA折叠景观拓扑结构以及构成这种多维景观基础的RNA结构特征的前所未有的视角。