Department of Physical Biochemistry, Max Planck Institute for Biophysical Chemistry, Goettingen, Germany.
Bioanalytical Mass Spectrometry Group, Max Planck Institute for Biophysical Chemistry, Goettingen, Germany.
Nat Commun. 2021 Mar 23;12(1):1830. doi: 10.1038/s41467-021-21942-6.
Aminoglycoside antibiotics target the ribosome and induce mistranslation, yet which translation errors induce bacterial cell death is unclear. The analysis of cellular proteins by quantitative mass spectrometry shows that bactericidal aminoglycosides induce not only single translation errors, but also clusters of errors in full-length proteins in vivo with as many as four amino acid substitutions in a row. The downstream errors in a cluster are up to 10,000-fold more frequent than the first error and independent of the intracellular aminoglycoside concentration. The prevalence, length, and composition of error clusters depends not only on the misreading propensity of a given aminoglycoside, but also on its ability to inhibit ribosome translocation along the mRNA. Error clusters constitute a distinct class of misreading events in vivo that may provide the predominant source of proteotoxic stress at low aminoglycoside concentration, which is particularly important for the autocatalytic uptake of the drugs.
氨基糖苷类抗生素以核糖体为靶点并诱导翻译错误,但哪种翻译错误会导致细菌细胞死亡尚不清楚。通过定量质谱分析细胞蛋白表明,杀菌性氨基糖苷类抗生素不仅诱导单个翻译错误,而且还在体内全长蛋白质中诱导多达四个氨基酸连续取代的错误簇。簇中的下游错误比第一个错误频繁 10000 倍以上,并且与细胞内氨基糖苷类浓度无关。错误簇的普遍性、长度和组成不仅取决于给定氨基糖苷的误读倾向,还取决于其抑制核糖体沿 mRNA 易位的能力。错误簇构成了体内一种独特的误读事件类别,它可能是低浓度氨基糖苷类药物引起蛋白毒性应激的主要来源,这对于药物的自动摄取尤其重要。