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从大量随机序列中分离新的核酶[见评论]

Isolation of new ribozymes from a large pool of random sequences [see comment].

作者信息

Bartel D P, Szostak J W

机构信息

Department of Molecular Biology, Massachusetts General Hospital, Boston 02114.

出版信息

Science. 1993 Sep 10;261(5127):1411-8. doi: 10.1126/science.7690155.

Abstract

An iterative in vitro selection procedure was used to isolate a new class of catalytic RNAs (ribozymes) from a large pool of random-sequence RNA molecules. These ribozymes ligate two RNA molecules that are aligned on a template by catalyzing the attack of a 3'-hydroxyl on an adjacent 5'-triphosphate--a reaction similar to that employed by the familiar protein enzymes that synthesize RNA. The corresponding uncatalyzed reaction also yields a 3',5'-phosphodiester bond. In vitro evolution of the population of new ribozymes led to improvement of the average ligation activity and the emergence of ribozymes with reaction rates 7 million times faster than the uncatalyzed reaction rate.

摘要

一种迭代体外筛选程序被用于从大量随机序列RNA分子中分离出一类新的催化RNA(核酶)。这些核酶通过催化3'-羟基对相邻5'-三磷酸的攻击,将两个在模板上对齐的RNA分子连接起来——这一反应类似于熟悉的合成RNA的蛋白质酶所采用的反应。相应的非催化反应也会产生3',5'-磷酸二酯键。新核酶群体的体外进化导致平均连接活性得到改善,并出现了反应速率比非催化反应速率快700万倍的核酶。

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