8P6P

Mycoplasma pneumoniae small ribosomal subunit in chloramphenicol-treated cells

8P6P の概要

• エントリーDOI: 10.2210/pdb8p6p/pdb
• EMDBエントリー: 17133
• 分子名称: 23S ribosomal RNA, 30S ribosomal protein S7, 30S ribosomal protein S8, ... (32 entities in total)
• 機能のキーワード: in situ, ribosome, chloramphenicol, cryo-et, translation
• 由来する生物種: Mycoplasmoides pneumoniae M129; 詳細
• タンパク質・核酸の鎖数: 26
• 化学式量合計: 1820423.88

構造登録者

Schacherl, M.,Xue, L.,Spahn, C.M.T.,Mahamid, J. (登録日: 2023-05-27, 公開日: 2024-11-20, 最終更新日: 2025-02-26)

主引用文献

Xue, L.,Spahn, C.M.T.,Schacherl, M.,Mahamid, J.
Structural insights into context-dependent inhibitory mechanisms of chloramphenicol in cells.
Nat.Struct.Mol.Biol., 32:257-267, 2025

PubMed Abstract: Ribosome-targeting antibiotics represent an important class of antimicrobial drugs. Chloramphenicol (Cm) is a well-studied ribosomal peptidyl transferase center (PTC) binder and growing evidence suggests that its inhibitory action depends on the sequence of the nascent peptide. How such selective inhibition on the molecular scale manifests on the cellular level remains unclear. Here, we use cryo-electron tomography to analyze the impact of Cm inside the bacterium Mycoplasma pneumoniae. By resolving the Cm-bound ribosomes to 3.0 Å, we elucidate Cm's coordination with natural nascent peptides and transfer RNAs in the PTC. We find that Cm leads to the accumulation of a number of translation elongation states, indicating ongoing futile accommodation cycles, and to extensive ribosome collisions. We, thus, suggest that, beyond its direct inhibition of protein synthesis, the action of Cm may involve the activation of cellular stress responses. This work exemplifies how in-cell structural biology can expand the understanding of mechanisms of action for extensively studied antibiotics.

PubMed: 39668257
DOI: 10.1038/s41594-024-01441-0

実験手法

ELECTRON MICROSCOPY (3.2 Å)