BINDING-SITES OF THE ANTIBIOTICS PACTAMYCIN AND CELESTICETIN ON RIBOSOMAL-RNAS

被引:33
作者
EGEBJERG, J
GARRETT, RA
机构
[1] UNIV COPENHAGEN,INST BIOL CHEM B,SOLVGADE 83,DK-1307 COPENHAGEN K,DENMARK
[2] AARHUS UNIV,INST CHEM,DK-8000 AARHUS,DENMARK
关键词
PACTAMYCIN; CELESTICETIN; RIBOSOMAL RNA; RIBOSOME FUNCTION;
D O I
10.1016/0300-9084(91)90158-W
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The binding sites of the antibiotics pactamycin and celesticetin on the rRNAs of Escherichia coli ribosomes were investigated by a chemical footprinting procedure. Pactamycin protected residues G-693 and C-795 in 16S RNA which are located in an important functional region of the 30S subunit participating in initiation complex formation and ribosomal subunit interaction. Celesticetin altered the reactivities of 5 residues A-2058, A-2059, A-2062, A-2451 and G-2505 within the central loop of domain V of 23S RNA which has been implicated in peptidyltransferase activity. Inferences are drawn concerning the mode of action of the antibiotics.
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页码:1145 / 1149
页数:5
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