An Efficient Cyclic Di-AMP Based Artificial Metalloribozyme for Enantioselective Diels-Alder Reactions

被引:6
作者
Qi, Qianqian [1 ]
Lv, Shuting [1 ]
Hao, Min [1 ]
Dong, Xingchen [1 ]
Gu, Youkun [1 ]
Wu, Peizhe [1 ]
Zhang, Wenyue [1 ]
Chen, Yashao [1 ]
Wang, Changhao [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Minist Educ, Key Lab Appl Surface & Colloid Chem, 620 West Changan Ave, Xian 710119, Peoples R China
基金
中国国家自然科学基金;
关键词
Metalloribozyme; C-di-AMP; Enantioselective catalysis; Diels-Alder reaction; Primordial chemistry; ASYMMETRIC CATALYSIS; MICHAEL ADDITION; DNA; GMP; NUCLEOTIDE; COMPLEXES; SCAFFOLD; RNA;
D O I
10.1002/ejoc.202000652
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The diverse structures of nucleic acids as scaffolds have brought the significant advancement for DNA-based enantioselective catalysis, yet RNA-based enantioselective catalysis is lacking investigation. Herein, we report a small, natural RNA of cyclic di-AMP (c-di-AMP) and Cu2+ ions assemble into an artificial metalloribozyme (c-di-AMP center dot Cu2+), that could effectively catalyze the enantioselective Diels-Alder reactions with up to 80 % ee. The enantioselective catalytic performance of c-di-AMP center dot Cu2+ has been studied by thorough investigations of different metal cofactors, c-di-AMP/Cu2+ molar ratios, additives, buffers and c-di-AMP analogues. In addition, the assembly of c-di-AMP center dot Cu2+ gives rise to 300-fold and 5-fold rate acceleration compared to the uncatalyzed reaction and Cu2+ ions, respectively. This work provides a simple and efficient strategy to construct the RNA-based catalysts that would expand the current nucleic acids-based catalysis and might hint the possible catalytic RNA in primordial chemistry.
引用
收藏
页码:4417 / 4424
页数:8
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