Journal of the American Chemical Society · 1997 · 95 citations · 16 references
PharmacyChemistryMolecular BiologyBioisosterismBioorthogonal ChemistryNucleic Acid ChemistryEnzyme InhibitionLigand BindingNucleic Acid SynthesisOligonucleotide ChemistryChemical Modification Of OligonucleotidesOligonucleotide Coupling ReactionsOligonucleotide Synthesis
Prebiotic syntheses of chiral monomers always yield racemic mixtures. Living systems, however, utilize L-amino acids and D-nucleotides in their biopolymers. The generation of optical asymmetry by selection and amplification in an autocatalytic process is, therefore, an important element in many theories of the origin of life. Replication of polynucleotides in template-directed syntheses is an obvious candidate for such an amplification step in a pre-'RNA world'. A serious objection to this suggestion is the observation that the efficiency of template-directed syntheses of RNA is limited by enantiomeric cross-inhibition. Peptide Nucleic Acids (PNAs), amide-linked, nonchiral analogues of RNA, have been 'copied' into RNA and constitute an alternative to chiral polynucleotides as an informational replicating system. Here, we use PNA as model for a hypothetical, nonchiral precursor of RNA in experiments re-examining enantiomeric cross-inhibition. We find that enantiomeric cross-inhibition is as serious in the polymerization of nucleotides on a PNA template as it is on a conventional RNA or DNA template.
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PNA hybridizes to complementary oligonucleotides obeying the Watson–Crick hydrogen-bonding rules
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