Zarrinkar P P, Williamson J R
Department of Chemistry, Massachusetts Institute of Technology, Cambridge 02139, USA.
Nat Struct Biol. 1996 May;3(5):432-8. doi: 10.1038/nsb0596-432.
We have probed the nature of the individual kinetic steps in the folding of the Tetrahymena ribozyme by studying the folding kinetics of mutant ribozymes. After rapid formation of the first structural subdomain, a slow step precedes stable formation of the second subdomain. The two central helices of the second subdomain form in an interdependent manner, and this structural subunit therefore also constitutes a kinetic folding unit. The slow folding step includes formation of tertiary interactions in a triple-helical scaffold that orients the two subdomains of the RNA. The rapid and early formation of short range secondary structure, the hierarchical formation of kinetic folding units corresponding to structural subdomains, and the formation of tertiary interactions between subdomains late during the folding process appear to be common features of the folding mechanism for both RNA and proteins.
我们通过研究突变型核酶的折叠动力学,探究了嗜热四膜虫核酶折叠过程中各个动力学步骤的本质。在第一个结构亚结构域快速形成后,一个缓慢步骤先于第二个亚结构域的稳定形成。第二个亚结构域的两个中心螺旋以相互依赖的方式形成,因此这个结构亚基也构成一个动力学折叠单元。缓慢的折叠步骤包括在一个三螺旋支架中形成三级相互作用,该支架使RNA的两个亚结构域定向。短程二级结构的快速早期形成、与结构亚结构域相对应的动力学折叠单元的分级形成,以及在折叠过程后期亚结构域之间三级相互作用的形成,似乎是RNA和蛋白质折叠机制的共同特征。