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7TTW

50S ribosomal subunit from Staphylococcus aureus containing double mutation in uL3 imparting linezolid resistance

7TTW の概要
エントリーDOI10.2210/pdb7ttw/pdb
関連するPDBエントリー7TTU
EMDBエントリー26125
分子名称50S ribosomal protein L19, 50S ribosomal protein L28, 50S ribosomal protein L29, ... (27 entities in total)
機能のキーワード50s subunit, antibiotic resistance, linezolid, ribosome
由来する生物種Staphylococcus aureus
詳細
タンパク質・核酸の鎖数27
化学式量合計1307599.65
構造登録者
Belousoff, M.J.,Piper, S.,Johnson, R. (登録日: 2022-02-02, 公開日: 2022-07-06, 最終更新日: 2025-05-14)
主引用文献Perlaza-Jimenez, L.,Tan, K.S.,Piper, S.J.,Johnson, R.M.,Bamert, R.S.,Stubenrauch, C.J.,Wright, A.,Lupton, D.,Lithgow, T.,Belousoff, M.J.
A Structurally Characterized Staphylococcus aureus Evolutionary Escape Route from Treatment with the Antibiotic Linezolid.
Microbiol Spectr, 10:e0058322-e0058322, 2022
Cited by
PubMed Abstract: Methicillin-resistant Staphylococcus aureus (MRSA) is a bacterial pathogen that presents great health concerns. Treatment requires the use of last-line antibiotics, such as members of the oxazolidinone family, of which linezolid is the first member to see regular use in the clinic. Here, we report a short time scale selection experiment in which strains of MRSA were subjected to linezolid treatment. Clonal isolates which had evolved a linezolid-resistant phenotype were characterized by whole-genome sequencing. Linezolid-resistant mutants were identified which had accumulated mutations in the ribosomal protein uL3. Multiple clones which had two mutations in uL3 exhibited resistance to linezolid, 2-fold higher than the clinical breakpoint. Ribosomes from this strain were isolated and subjected to single-particle cryo-electron microscopic analysis and compared to the ribosomes from the parent strain. We found that the mutations in uL3 lead to a rearrangement of a loop that makes contact with Helix 90, propagating a structural change over 15 Å away. This distal change swings nucleotide U2504 into the binding site of the antibiotic, causing linezolid resistance. Antibiotic resistance poses a critical problem to human health and decreases the utility of these lifesaving drugs. Of particular concern is the "superbug" methicillin-resistant Staphylococcus aureus (MRSA), for which treatment of infection requires the use of last-line antibiotics, including linezolid. In this paper, we characterize the atomic rearrangements which the ribosome, the target of linezolid, undergoes during its evolutionary journey toward becoming drug resistant. Using cryo-electron microscopy, we describe a particular molecular mechanism which MRSA uses to become resistant to linezolid.
PubMed: 35736238
DOI: 10.1128/spectrum.00583-22
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (2.9 Å)
構造検証レポート
Validation report summary of 7ttw
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-04-15に公開中

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