Abstract
3H-puromycin binds to bacterial ribosomes, in the presence of ethanol, under the experimental conditions of the fragment reaction assay. The binding is feeble, takes place at 0°C, is partially inhibited by chloramphenicol and lincomycin and totally by sparsomycin. 3H-puromycin binding is hardly affected by the 3′ aminonucleoside of puromycin, is well inhibited by the L-Phenylalanine and L-Leucine analogues of puromycin and totally blocked by L-Phenylalanyl-adenosine.
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Fernandez-Muñoz, R., Vazquez, D. Binding of puromycin to E. coli ribosomes. Effects of puromycin analogues and peptide bond formation inhibitors. Molecular Biology Reports 1, 27–32 (1973). https://doi.org/10.1007/BF00357402
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DOI: https://doi.org/10.1007/BF00357402