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

被引:158
作者
Serganov, A
Keiper, S
Malinina, L
Tereshko, V
Skripkin, E
Höbartner, C
Polonskaia, A
Phan, AT
Wombacher, R
Micura, R
Dauter, Z
Jäschke, A
Patel, DJ
机构
[1] Heidelberg Univ, Inst Pharm & Mol Biotechnol, D-69120 Heidelberg, Germany
[2] Mem Sloan Kettering Canc Ctr, Struct Biol Program, New York, NY 10021 USA
[3] Leopold Franzens Univ, Inst Organ Chem, Ctr Mol Biosci, A-6020 Innsbruck, Austria
[4] Brookhaven Natl Lab, Synchrotron Radiat Res Sect, NCI, Upton, NY 11973 USA
关键词
D O I
10.1038/nsmb906
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 -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.
引用
收藏
页码:218 / 224
页数:7
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