Aminoacyl esterase activity of the Tetrahymena ribozyme
- PMID: 1604316
- DOI: 10.1126/science.1604316
Aminoacyl esterase activity of the Tetrahymena ribozyme
Abstract
Several classes of ribozymes (catalytic RNA's) catalyze reactions at phosphorus centers, but apparently no reaction at a carbon center has been demonstrated. The active site of the Tetrahymena ribozyme was engineered to bind an oligonucleotide derived from the 3' end of N-formyl-methionyl-tRNA(fMet). This ribozyme catalyzes the hydrolysis of the aminoacyl ester bond to a modest extent, 5 to 15 times greater than the uncatalyzed rate. Catalysis involves binding of the oligonucleotide to the internal guide sequence of the ribozyme and requires Mg2+ and sequence elements of the catalytic core. The ability of RNA to catalyze reactions with aminoacyl esters expands the catalytic versatility of RNA and suggests that the first aminoacyl tRNA synthetase could have been an RNA molecule.
Comment in
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Finding RNA makes proteins gives 'RNA world' a big boost.Science. 1992 Jun 5;256(5062):1396-7. doi: 10.1126/science.1376495. Science. 1992. PMID: 1376495 No abstract available.
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New horizons for RNA catalysis.Science. 1992 Jun 5;256(5062):1402-3. doi: 10.1126/science.1376496. Science. 1992. PMID: 1376496 No abstract available.
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