Puromycin reaction of the A-site bound peptidyl-tRNA
AcPhe 2-tRNA Phe which appears in ribosomes after consecutive binding of AcPhe-tRNA Phe at the P sites and EF-Tu-directed binding of Phe-tRNA Phe at the A sites is able to react quantitatively with puromycin in the absence of EF-G. One could readily explain this fact to be the consequence of spontan...
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Veröffentlicht in: | Biochimie 1992-05, Vol.74 (5), p.411-417 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | AcPhe
2-tRNA
Phe which appears in ribosomes after consecutive binding of AcPhe-tRNA
Phe at the P sites and EF-Tu-directed binding of Phe-tRNA
Phe at the A sites is able to react quantitatively with puromycin in the absence of EF-G. One could readily explain this fact to be the consequence of spontaneous translocation. However, a detailed study of kinetics of puromycin reaction carried out with the use of viomycin (inhibitor of translocation) and the P-site test revealed that, apart from spontaneous translocation, this peptidyl-tRNA could react with puromycin being located at the A site. This leads to the conclusion that the transpeptidation reaction triggers conformational changes in the A-site ribosomal complex bringing the 3′-end of a newly synthesized peptidyl-tRNA nearer to the peptidyl site of peptidyltransferase center. This is detected functionally as a highly pronounced ability of such a peptidyl-tRNA to react with puromycin. |
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ISSN: | 0300-9084 1638-6183 |
DOI: | 10.1016/0300-9084(92)90080-X |