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现在位置:首页 > 科研进展 > 最新重要论文(影响因子PNAS及以上)
The Molecular Architecture for RNA-Guided RNA Cleavage by Cas13a, Cell, Volume 170, Issue 4, p714–726.e10, 10 August 2017
2017-07-28 | 【     】【打印】【关闭

Cell, Volume 170, Issue 4, p714–726.e10, 10 August 2017 ,DOI: http://dx.doi.org/10.1016/j.cell.2017.06.050

The Molecular Architecture for RNA-Guided RNA Cleavage by Cas13a

Liang Liu, Xueyan Li,Jun Ma,Zongqiang Li,Lilan You,Jiuyu Wang,Min Wang,Xinzheng Zhang,Yanli Wang

Summary
Cas13a, a type VI-A CRISPR-Cas RNA-guided RNA ribonuclease, degrades invasive RNAs targeted by CRISPR RNA (crRNA) and has potential applications in RNA technology. To understand how Cas13a is activated to cleave RNA, we have determined the crystal structure of Leptotrichia buccalis (Lbu) Cas13a bound to crRNA and its target RNA, as well as the cryo-EM structure of the LbuCas13a-crRNA complex. The crRNA-target RNA duplex binds in a positively charged central channel of the nuclease (NUC) lobe, and Cas13a protein and crRNA undergo a significant conformational change upon target RNA binding. The guide-target RNA duplex formation triggers HEPN1 domain to move toward HEPN2 domain, activating the HEPN catalytic site of Cas13a protein, which subsequently cleaves both single-stranded target and collateral RNAs in a non-specific manner. These findings reveal how Cas13a of type VI CRISPR-Cas systems defend against RNA phages and set the stage for its development as a tool for RNA manipulation.

相关报道:http://www.ibp.cas.cn/kyjz/zxdt/201707/t20170728_4837620.html

文章链接:http://www.cell.com/cell/fulltext/S0092-8674(17)30769-9

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