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源自随机RNA序列的结构复杂且活性高的RNA连接酶。

Structurally complex and highly active RNA ligases derived from random RNA sequences.

作者信息

Ekland E H, Szostak J W, Bartel D P

机构信息

Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.

出版信息

Science. 1995 Jul 21;269(5222):364-70. doi: 10.1126/science.7618102.

Abstract

Seven families of RNA ligases, previously isolated from random RNA sequences, fall into three classes on the basis of secondary structure and regiospecificity of ligation. Two of the three classes of ribozymes have been engineered to act as true enzymes, catalyzing the multiple-turnover transformation of substrates into products. The most complex of these ribozymes has a minimal catalytic domain of 93 nucleotides. An optimized version of this ribozyme has a kcat exceeding one per second, a value far greater than that of most natural RNA catalysts and approaching that of comparable protein enzymes. The fact that such a large and complex ligase emerged from a very limited sampling of sequence space implies the existence of a large number of distinct RNA structures of equivalent complexity and activity.

摘要

先前从随机RNA序列中分离出的七类RNA连接酶,根据连接的二级结构和区域特异性可分为三类。三类核酶中的两类已被设计成真正的酶,催化底物向产物的多轮转化。这些核酶中最复杂的一种具有93个核苷酸的最小催化结构域。这种核酶的优化版本的催化常数超过每秒一次,该值远大于大多数天然RNA催化剂,接近同类蛋白质酶的催化常数。如此大且复杂的连接酶从非常有限的序列空间采样中出现,这一事实意味着存在大量具有同等复杂性和活性的不同RNA结构。

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