Context-specific action of antibiotics targeting the catalytic center of the bacterial ribosome

针对细菌核糖体催化中心的抗生素的特定作用

基本信息

  • 批准号:
    9332339
  • 负责人:
  • 金额:
    $ 39.98万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2016
  • 资助国家:
    美国
  • 起止时间:
    2016-08-15 至 2020-07-31
  • 项目状态:
    已结题

项目摘要

Antibiotics that inhibit cell growth by interfering with protein synthesis have been among the most clinically successful antibacterials. In spite of the importance of these inhibitors, there are significant gaps in our understanding of the most fundamental principles of their action. Many of the protein synthesis inhibitors, from the classic chloramphenicol (CHL) to the newer linezolid (LZD), bind at the catalytic peptidyl transferase center (PTC) of the ribosome, where they clash with the placement of aminoacyl-tRNA. Because of the location of their binding site, it is commonly assumed that they inhibit translation by interfering with formation of every peptide bond, either at the start codon or at any of the internal codons of a gene. However, our preliminary data show that this view is principally incorrect. Instead of indiscriminately inhibiting peptide bond formation, CHL and LZD stall elongation of translation only at specific mRNA sites. The nature of the nascent peptide chain appears to play the major role in specifying the sites of translation arrest, but the general rules that define the sites of stalling and the molecular mechanisms that underlie this effect remain unknown. Therefore, the main goal of this project is to gain a detailed understanding of the context specific action of PTC-targeting antibiotics. The study will primarily focus on LZD and CHL. LZD is the first and most broadly medically used oxazolidinone. CHL is one of the oldest known ribosomal antibiotics. In spite of its reduced medical importance, inclusion of CHL in the study is crucial, not only because of the vast amount of information available for this inhibitor, but also to contrast its context specific action with that of LZD and correlate the effects with individual structural properties of the drugs. In Specific Aim 1, whole-cell ribosome profiling and quantitative biochemical testing will be used to identify the detailed requirements for the sequence context that defines the preferred sites of inhibition of translation by LZD or CHL. In Specific Aim 2, an array of biochemical, structural and genetic approaches will be employed to understand the molecular mechanisms that account for the context-specific action of the PTC- targeting inhibitors. The use of innovative techniques, such as single molecule FRET or an engineered tethered ribosome, are expected to provide principally new insights into the most fundamental aspects of action of the inhibitors of the ribosomal catalytic center. Specific Aim 3 will address a conceptually important and medically-relevant question, whether context specificity of drug action results into protein-specific inhibition of translation by the PTC-targeting antibiotics. The anticipated findings should significantly expand the understanding of the general mode of action of clinically-important antibacterials that act upon the catalytic center of the ribosome and may open new venues for rational development of protein synthesis inhibitors with superior antibiotic properties.
通过干扰蛋白质合成来抑制细胞生长的抗生素一直是最常用的抗生素之一。 临床上成功的抗菌药物。尽管这些抑制剂很重要,但在 我们对他们行动的最基本原则的理解。许多蛋白质合成抑制剂, 从经典的氯霉素(CHL)到较新的利奈唑胺(LZD),在催化肽基转移酶处结合 中心(PTC)的核糖体,在那里他们与氨酰-tRNA的位置冲突。因为 由于其结合位点的位置,通常认为它们通过干扰蛋白质的形成来抑制翻译。 每一个肽键,无论是在起始密码子还是在基因的任何内部密码子。但我们的 初步资料表明,这种看法基本上是不正确的。而不是不加选择地抑制肽键 形成,CHL和LZD仅在特定的mRNA位点停止翻译延伸。新生的本质 肽链似乎在指定翻译停滞位点方面起主要作用,但一般规则 确定失速位置的分子机制和这种效应的基础仍然是未知的。 因此,本项目的主要目标是详细了解特定于上下文的操作 PTC靶向抗生素。该研究将主要关注LZD和CHL。LZD是第一个也是最广泛的 医用恶唑烷酮。CHL是已知最古老的核糖体抗生素之一。尽管其减少 医学上的重要性,将CHL纳入研究至关重要,不仅是因为大量的信息 可用于这种抑制剂,而且还将其背景特异性作用与LZD的作用进行对比,并将LZD的作用与LZD的作用相关联。 影响药物的个体结构特性。 在具体目标1中,将使用全细胞核糖体分析和定量生化检测, 确定序列背景的详细要求,该序列背景定义了以下抑制的优选位点: LZD或CHL翻译。在具体目标2中,一系列生物化学,结构和遗传方法将 被用来理解的分子机制,占特定的背景行动的PTC- 靶向抑制剂。使用创新技术,如单分子FRET或工程化的 系留核糖体,预计将提供主要的新见解,最基本的方面, 核糖体催化中心抑制剂的作用。具体目标3将解决一个概念上重要的问题, 和医学相关的问题,药物作用的背景特异性是否导致蛋白质特异性抑制 的翻译。 预期的研究结果应大大扩大对一般作用模式的理解, 作用于核糖体催化中心并可能打开新途径的临床重要抗菌药物 用于合理开发具有上级抗生素特性的蛋白质合成抑制剂。

项目成果

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ALEXANDER S MANKIN其他文献

ALEXANDER S MANKIN的其他文献

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{{ truncateString('ALEXANDER S MANKIN', 18)}}的其他基金

Advancing ribosome-targeting antibacterial peptides with a unique mechanism of action
以独特的作用机制推进核糖体靶向抗菌肽
  • 批准号:
    10443921
  • 财政年份:
    2022
  • 资助金额:
    $ 39.98万
  • 项目类别:
Advancing ribosome-targeting antibacterial peptides with a unique mechanism of action
以独特的作用机制推进核糖体靶向抗菌肽
  • 批准号:
    10569098
  • 财政年份:
    2022
  • 资助金额:
    $ 39.98万
  • 项目类别:
Advancing ribosome-targeting antibacterial peptides with a unique mechanism of action
以独特的作用机制推进核糖体靶向抗菌肽
  • 批准号:
    10436039
  • 财政年份:
    2021
  • 资助金额:
    $ 39.98万
  • 项目类别:
Equipment Supplement Request for Purchasing Amersham Typhoon RGB Phosphorimager (for R35GM127134)
购买 Amersham Typhoon RGB 荧光成像仪(适用于 R35GM127134)的设备补充申请
  • 批准号:
    10386084
  • 财政年份:
    2018
  • 资助金额:
    $ 39.98万
  • 项目类别:
Exploiting antibiotics to understand the ribosome and translation
利用抗生素来了解核糖体和翻译
  • 批准号:
    10366000
  • 财政年份:
    2018
  • 资助金额:
    $ 39.98万
  • 项目类别:
Exploiting antibiotics to understand the ribosome and translation
利用抗生素来了解核糖体和翻译
  • 批准号:
    9897557
  • 财政年份:
    2018
  • 资助金额:
    $ 39.98万
  • 项目类别:
Context-specific action of antibiotics targeting the catalytic center of the bacterial ribosome
针对细菌核糖体催化中心的抗生素的特定作用
  • 批准号:
    9158354
  • 财政年份:
    2016
  • 资助金额:
    $ 39.98万
  • 项目类别:
Molecular mechanisms of action of macrolide antibiotics
大环内酯类抗生素的分子作用机制
  • 批准号:
    8482422
  • 财政年份:
    2013
  • 资助金额:
    $ 39.98万
  • 项目类别:
Molecular mechanisms of action of macrolide antibiotics
大环内酯类抗生素的分子作用机制
  • 批准号:
    8640960
  • 财政年份:
    2013
  • 资助金额:
    $ 39.98万
  • 项目类别:
Programmed translation arrest controlled by nascent peptides and antibiotics
由新生肽和抗生素控制的程序化翻译停滞
  • 批准号:
    8917273
  • 财政年份:
    2012
  • 资助金额:
    $ 39.98万
  • 项目类别:

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