Amicoumacin A induces cancer cell death by targeting the eukaryotic ribosome

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作者
Irina V. Prokhorova
Kseniya A. Akulich
Desislava S. Makeeva
Ilya A. Osterman
Dmitry A. Skvortsov
Petr V. Sergiev
Olga A. Dontsova
Gulnara Yusupova
Marat M. Yusupov
Sergey E. Dmitriev
机构
[1] Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC),Department of Chemistry
[2] INSERM U964,Department of Biochemistry
[3] CNRS UMR7104,undefined
[4] Université de Strasbourg,undefined
[5] Belozersky Institute of Physico-Chemical Biology,undefined
[6] Lomonosov Moscow State University,undefined
[7] School of Bioengineering and Bioinformatics,undefined
[8] Lomonosov Moscow State University,undefined
[9] Lomonosov Moscow State University,undefined
[10] Engelhardt Institute of Molecular Biology,undefined
[11] Russian Academy of Sciences,undefined
[12] Biological Faculty,undefined
[13] Lomonosov Moscow State University,undefined
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摘要
Amicoumacin A is an antibiotic that was recently shown to target bacterial ribosomes. It affects translocation and provides an additional contact interface between the ribosomal RNA and mRNA. The binding site of amicoumacin A is formed by universally conserved nucleotides of rRNA. In this work, we showed that amicoumacin A inhibits translation in yeast and mammalian systems by affecting translation elongation. We determined the structure of the amicoumacin A complex with yeast ribosomes at a resolution of 3.1  Å. Toxicity measurement demonstrated that human cancer cell lines are more susceptible to the inhibition by this compound as compared to non-cancerous ones. This might be used as a starting point to develop amicoumacin A derivatives with clinical value.
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