Abstract
We describe the allosteric control of Diels-Alder reactions by a small organic effector, theophylline. This is achieved by converting a Diels-Alder ribozyme into an allosterically regulated system. In contrast to other published systems, we have a bond-forming reaction with two small-molecule substrates and multiple turnover. This system could be very attractive for the development of assays for a variety of analytes and can be regarded as a prototype of fully synthetic signaling cascades.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Anthracenes / chemistry*
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Base Sequence
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Biotin / chemistry
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Catalysis
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DNA-Directed RNA Polymerases / chemistry
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Kinetics
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Maleimides / chemistry*
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Molecular Sequence Data
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Nucleic Acid Conformation
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Nucleotides / chemistry
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RNA / chemistry*
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RNA, Catalytic / chemistry*
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RNA, Catalytic / metabolism
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Theophylline / chemistry
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Viral Proteins / chemistry
Substances
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Anthracenes
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Maleimides
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Nucleotides
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RNA, Catalytic
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Viral Proteins
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RNA
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Biotin
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Theophylline
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bacteriophage T7 RNA polymerase
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DNA-Directed RNA Polymerases
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anthracene