Scott W G, Finch J T, Klug A
Medical Research Council, Laboratory of Molecular Biology, Cambridge, England.
Cell. 1995 Jun 30;81(7):991-1002. doi: 10.1016/s0092-8674(05)80004-2.
We have solved the crystal structure of an all-RNA hammerhead ribozyme having a single 2'-O-methyl cytosine incorporated at the active site to prevent cleavage. The conditions used differ from those in another recent solution in four significant ways: first, it is an all-RNA ribozyme rather than a DNA-RNA hybrid; second, the connectivity of the ribozyme backbone strands is different; third, the crystals were grown in the presence of a much lower concentration of salt; and fourth, the crystal packing scheme is very different. Nevertheless, the three-dimensional structure of the all-RNA hammerhead ribozyme is similar to the previous structure. Five potential Mg(II)-binding sites are identified, including one positioned near the ribozyme catalytic pocket. Upon this basis, as well as upon comparisons with the metal-binding sites in the structurally homologous uridine turn of tRNAPhe, we propose a mechanism for RNA catalytic cleavage.
我们解析了一种全RNA锤头状核酶的晶体结构,该核酶在活性位点掺入了单个2'-O-甲基胞嘧啶以防止切割。所采用的条件在四个重要方面与最近的另一种解决方案不同:第一,它是全RNA核酶而非DNA-RNA杂交体;第二,核酶主链链的连接方式不同;第三,晶体在盐浓度低得多的情况下生长;第四,晶体堆积方式非常不同。尽管如此,全RNA锤头状核酶的三维结构与先前的结构相似。鉴定出五个潜在的Mg(II)结合位点,其中一个位于核酶催化口袋附近。基于此以及与苯丙氨酸tRNA结构同源的尿苷转角中的金属结合位点的比较,我们提出了RNA催化切割的机制。