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Revisiting the bacterial cell wall as a target for new antibiotics

Revisiting the bacterial cell wall as a target for new antibiotics
重新审视细菌细胞壁作为新抗生素的靶标
批准号:
8146696
负责人:
DOUGLAS Benjamin WEIBEL
金额:
$225.75万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-30 至 2016-06-30

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DESCRIPTION (Provided by the applicant) Abstract: Bacteria use the cell wall to control the organization of many sub-cellular components in space and time. The cell wall functions as the 'cytoskeleton' in bacteria and protects cells from mechanical stress. The enormous osmotic pressure across the cell wall (>1 atm) requires that cell growth be tightly regulated, as small defects in the cell wall are catastrophic. A molecular understanding of the assembly, properties, and mechanisms for localizing essential proteins to the cell wall will provide fundamental insight into the inner working of this essential structure. The identification of proteins that are localized to the cell wall and regulate and remodel it will open the door to a new chapter in antibiotic development by rebooting an interest in this cellular material as a drug target. My laboratory will use a multidisciplinary approach to study the bacterial cell wall by drawing on our experience in chemical biology, biochemistry, biophysics, and materials science and engineering. Our focus centers upon two aims: 1. We will develop a high-throughput, materials science-based technique for measuring the mechanical properties of bacterial cell walls. Using this capability we will analyze the entire genome-wide collection of Escherichia coli single gene mutants to identify proteins that modulate its physical properties. 2. We will develop a suite of materials science-based approaches for controlling cell wall curvature in bacteria and will study how the shape of the cell wall regulates the formation of lipid microdomains, which in turn participates in the intracellular localization of cytoplasmic proteins. We will develop small molecules that target the proteins identified in these aims and will use them to study the function of these molecules in vivo using a chemical biological approach. The results of these studies will shed new light on essential processes in bacterial cells and will uncover mechanisms for regulating bacterial physiology. These mechanisms and molecules will stimulate the development of potent classes of antibiotics that have applications in preventing and treating human infections. Public Health Relevance: This research will identify new proteins and mechanisms that regulate the structure and organization of the bacterial cell wall. The results will lead to the development of new classes of antibiotics against pathogenic bacteria.
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DETERMINING THE DISSOCIATION CONSTANT OF A22 TO THE BACTERIAL CYTOSKELETON MREB
  • 批准号:
    8168942
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2010
  • 负责人:
    DOUGLAS Benjamin WEIBEL
  • 依托单位:
TRAINING IN THE USE OF BRUKER AND VARIAN SPECTROMETERS AND NMR
  • 批准号:
    8168954
  • 项目类别:
  • 资助金额:
    $0.01万
  • 财政年份:
    2010
  • 负责人:
    DOUGLAS Benjamin WEIBEL
  • 依托单位:
DETERMINING THE DISSOCIATION CONSTANT OF A22 TO THE BACTERIAL CYTOSKELETON MREB
  • 批准号:
    7954615
  • 项目类别:
  • 资助金额:
    $0.59万
  • 财政年份:
    2009
  • 负责人:
    DOUGLAS Benjamin WEIBEL
  • 依托单位:
TRAINING IN THE USE OF BRUKER AND VARIAN SPECTROMETERS AND NMR
  • 批准号:
    7954640
  • 项目类别:
  • 资助金额:
    $0.01万
  • 财政年份:
    2009
  • 负责人:
    DOUGLAS Benjamin WEIBEL
  • 依托单位:
国内基金
海外基金
Segmented Filamentous Bacteria激活宿主免疫系统抑制其拮抗菌 Enterobacteriaceae维持菌群平衡及其机制研究
  • 批准号:
    81971557
  • 项目类别:
    面上项目
  • 资助金额:
    65.0万元
  • 批准年份:
    2019
  • 负责人:
    毛开睿
  • 依托单位:
电缆细菌(Cable bacteria)对水体沉积物有机污染的响应与调控机制