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The toxin colicin E3 targets the 30S subunit of bacterial ribosomes and cleaves a phosphodiester bond in the decoding center. We present the crystal structure of the 70S ribosome in complex with the cytotoxic domain of colicin E3 (E3-rRNase). The structure reveals how the rRNase domain of colicin binds to the A site of the decoding center in the 70S ribosome and cleaves the 16S ribosomal RNA (rRNA) between A1493 and G1494. The cleavage mechanism involves the concerted action of conserved residues Glu62 and His58 of the cytotoxic domain of colicin E3. These residues activate the 16S rRNA for 2' OH-induced hydrolysis. Conformational changes observed for E3-rRNase, 16S rRNA and helix 69 of 23S rRNA suggest that a dynamic binding platform is required for colicin E3 binding and function.

Original publication

DOI

10.1038/nsmb.1896

Type

Journal article

Journal

Nat Struct Mol Biol

Publication Date

10/2010

Volume

17

Pages

1241 - 1246

Keywords

Amino Acid Sequence, Catalysis, Colicins, Conserved Sequence, Crystallography, X-Ray, Escherichia coli, Macromolecular Substances, Models, Molecular, Molecular Sequence Data, Nucleic Acid Conformation, Protein Conformation, Protein Structure, Tertiary, RNA, Messenger, RNA, Ribosomal, 16S, RNA, Ribosomal, 23S, RNA, Transfer, Met, Ribosomes, Sequence Alignment, Sequence Homology, Amino Acid, Structure-Activity Relationship, Thermus thermophilus