Structure and engineering of Brevibacillus laterosporus Cas9

被引:0
|
作者
Nakane, Toshihiro [1 ]
Nakagawa, Ryoya [1 ]
Ishiguro, Soh [2 ,3 ]
Okazaki, Sae [4 ]
Mori, Hideto [5 ,6 ,7 ]
Shuto, Yutaro [1 ]
Yamashita, Keitaro [4 ]
Yachie, Nozomu [2 ,3 ,7 ,8 ]
Nishimasu, Hiroshi [4 ,9 ,10 ]
Nureki, Osamu [1 ]
机构
[1] Univ Tokyo, Grad Sch Sci, Dept Biol Sci, 7-3-1 Hongo,Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ British Columbia, Sch Biomed Engn, Fac Sci Appl, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Fac Med, Vancouver, BC V6S 0L4, Canada
[4] Univ Tokyo, Res Ctr Adv Sci & Technol, Struct Biol Div, 4-6-1 Komaba,Meguro ku, Tokyo 1538904, Japan
[5] Keio Univ, Inst Adv Biosci, Yamagata 9970035, Japan
[6] Keio Univ, Grad Sch Media & Governance, Fujisawa, Kanagawa 2520882, Japan
[7] Osaka Univ, Premium Res Inst Human Metaverse Med WPI PRIMe, Suita, Osaka 5650871, Japan
[8] Univ Tokyo, Res Ctr Adv Sci & Technol, Synthet Biol Div, Tokyo 1538904, Japan
[9] Univ Tokyo, Grad Sch Engn, Dept Chem & Biotechnol, 7-3-1 Hongo,Bunkyo-ku, Tokyo 1138656, Japan
[10] Inamori Res Inst Sci, 620 Suiginya Cho,Shimogyo Ku, Kyoto 6008411, Japan
关键词
CRYSTAL-STRUCTURE; RNA; CRISPR-CAS9; INTEGRATION; COMPLEX;
D O I
10.1038/s42003-024-06422-z
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The RNA-guided DNA endonuclease Cas9 cleaves double-stranded DNA targets complementary to an RNA guide, and is widely used as a powerful genome-editing tool. Here, we report the crystal structure of Brevibacillus laterosporus Cas9 (BlCas9, also known as BlatCas9), in complex with a guide RNA and its target DNA at 2.4-& Aring; resolution. The structure reveals that the BlCas9 guide RNA adopts an unexpected architecture containing a triple-helix, which is specifically recognized by BlCas9, and that BlCas9 recognizes a unique N4CNDN protospacer adjacent motif through base-specific interactions on both the target and non-target DNA strands. Based on the structure, we rationally engineered a BlCas9 variant that exhibits enhanced genome- and base-editing activities with an expanded target scope in human cells. This approach may further improve the performance of the enhanced BlCas9 variant to generate useful genome-editing tools that require only a single C PAM nucleotide and can be packaged into a single AAV vector for in vivo gene therapy.
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收藏
页数:10
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