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Structural basis for Diels-Alder ribozyme-catalyzed carbon-carbon bond formation

机译:Diels-Alder核酶催化的碳-碳键形成的结构基础

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摘要

The majority of structural efforts addressing RNA’s catalytic function have focused on natural ribozymes, which catalyze phosphodiester transfer reactions. By contrast, little is known about how RNA catalyzes other types of chemical reactions. We report here the crystal structures of a ribozyme that catalyzes enantioselective carbon-carbon bond formation by the Diels-Alder reaction in the unbound state and in complex with a reaction product. The RNA adopts a λ-shaped nested pseudoknot architecture whose preformed hydrophobic pocket is precisely complementary in shape to the reaction product. RNA folding and product binding are dictated by extensive stacking and hydrogen bonding, whereas stereoselection is governed by the shape of the catalytic pocket. Catalysis is apparently achieved by a combination of proximity, complementarity and electronic effects. We observe structural parallels in the independently evolved catalytic pocket architectures for ribozyme- and antibody-catalyzed Diels-Alder carbon-carbon bond-forming reactions.
机译:解决RNA催化功能的大部分结构努力都集中在天然核酶上,该酶催化磷酸二酯转移反应。相比之下,人们对RNA如何催化其他类型的化学反应了解甚少。我们在这里报告了核酶的晶体结构,该酶通过未结合状态并与反应产物复合的Diels-Alder反应催化对映选择性碳-碳键形成。 RNA采用λ形嵌套假结结构,其预先形成的疏水袋在形状上与反应产物精确互补。 RNA折叠和产物结合取决于广泛的堆积和氢键,而立体选择则取决于催化袋的形状。催化作用显然是通过邻近性,互补性和电子效应的组合来实现的。我们观察到核酶和抗体催化的Diels-Alder碳-碳键形成反应的独立进化的催化口袋结构中的结构相似性。

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