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7SA4

Damaged 70S ribosome with PrfH bound

This is a non-PDB format compatible entry.
Summary for 7SA4
Entry DOI10.2210/pdb7sa4/pdb
EMDB information24944
Descriptor23S ribosomal RNA, 50S ribosomal protein L5, 50S ribosomal protein L6, ... (60 entities in total)
Functional Keywordsprfh, damaged ribosome, ribotoxin, ribosome
Biological sourceEscherichia coli
More
Total number of polymer chains58
Total formula weight2261985.96
Authors
Tian, Y.,Zeng, F.,Raybarman, A.,Carruthers, A.,Li, Q.,Fatma, S.,Huang, R.H. (deposition date: 2021-09-22, release date: 2022-08-03, Last modification date: 2025-03-19)
Primary citationTian, Y.,Zeng, F.,Raybarman, A.,Fatma, S.,Carruthers, A.,Li, Q.,Huang, R.H.
Sequential rescue and repair of stalled and damaged ribosome by bacterial PrfH and RtcB.
Proc.Natl.Acad.Sci.USA, 119:e2202464119-e2202464119, 2022
Cited by
PubMed Abstract: RtcB is involved in transfer RNA (tRNA) splicing in archaeal and eukaryotic organisms. However, most RtcBs are found in bacteria, whose tRNAs have no introns. Because tRNAs are the substrates of archaeal and eukaryotic RtcB, it is assumed that bacterial RtcBs are for repair of damaged tRNAs. Here, we show that a subset of bacterial RtcB, denoted RtcB2 herein, specifically repair ribosomal damage in the decoding center. To access the damage site for repair, however, the damaged 70S ribosome needs to be dismantled first, and this is accomplished by bacterial PrfH. Peptide-release assays revealed that PrfH is only active with the damaged 70S ribosome but not with the intact one. A 2.55-Å cryo-electron microscopy structure of PrfH in complex with the damaged 70S ribosome provides molecular insight into PrfH discriminating between the damaged and the intact ribosomes via specific recognition of the cleaved 3'-terminal nucleotide. RNA repair assays demonstrated that RtcB2 efficiently repairs the damaged 30S ribosomal subunit but not the damaged tRNAs. Cell-based assays showed that the RtcB2-PrfH pair reverse the damage inflicted by ribosome-specific ribotoxins in vivo. Thus, our combined biochemical, structural, and cell-based studies have uncovered a bacterial defense system specifically evolved to reverse the lethal ribosomal damage in the decoding center for cell survival.
PubMed: 35858322
DOI: 10.1073/pnas.2202464119
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.55 Å)
Structure validation

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