Elucidation of Pathways: Bacterial and Mass Spectrometric Studies

途径阐明:细菌和质谱研究

基本信息

  • 批准号:
    RGPIN-2014-04536
  • 负责人:
  • 金额:
    $ 2.19万
  • 依托单位:
  • 依托单位国家:
    加拿大
  • 项目类别:
    Discovery Grants Program - Individual
  • 财政年份:
    2014
  • 资助国家:
    加拿大
  • 起止时间:
    2014-01-01 至 2015-12-31
  • 项目状态:
    已结题

项目摘要

Bacteria are intimately associated with the human body; beneficial bacteria support health and well-being by aiding digestion, protecting against infection, and stimulating the immune system. Substances produced by bacteria, known as metabolites, act as molecular signals defining the bacterium-host relationship. To potentially benefit the quality of life by revealing new directions for the treatment of disease, our approach is to thoroughly study Fusobacterium varium, a bacterium typically found in the intestines of animals that may contribute to the initiation of bowel disease. Our research program also focuses on chemical processes associated with mass spectrometry, a technique in which molecules are first charged and then broken into pieces upon input of energy. The specific pieces formed are diagnostic, providing a basis for the identification of drugs, environmental contaminants and explosives in various situations and allowing conclusions to be drawn that have broad implications (e.g., the use of banned substances in sports). To develop a deeper understanding of fundamentals behind these important applications, we choose substances that mimic the structures of current drugs and drug candidates, and can accommodate charge in more than one location, increasing their likelihood to break apart in two or more different ways (i.e., fragmentation pathways). With our interpretative developments, mass spectrometry will provide enriched and more reliable information, increasing its value as an essential tool for the characterization of drug metabolites and shortening the time needed to complete this essential step in the development of prospective new drugs. As a complement to genetic studies, our on-going chemical research has demonstrated metabolic diversity in the intestinal bacterium leading to the production of eight substances, of which one may have an unanticipated function as a molecular signal with implications in bowel disease. By identifying the pathways used to form these metabolites, unique metabolic processes in anaerobic bacteria can be evaluated as targets for selective metabolic inhibitors, a novel rational design strategy for the generation of lead compounds for novel antibiotics effective against pathogenic bacteria resistant to current antibiotic treatments. Also, three of the bacterial metabolites excreted have important practical applications as sustainable chemical feed stocks used, for example, in the manufacture of biodegradable polymers with biomedical applications. In this application, funding is requested to pursue two seemingly diverse research investigations. However, commonalities in the thought process of our mechanistic investigative approach to pathway elucidation and the nature of the substances studied provide significant overlap. For each, we design and synthesize probes to test pathway hypotheses, collect evidence using substances labelled with stable isotopes, and logically assimilate the evidence to provide a reliable description of each pathway. Overall, we tackle fundamental questions in the relationship between intestinal bacteria and human hosts, a complex and relatively unexplored area at the intersection of bacterium and human metabolism. Our research program in fundamental science will offer new insights for the interpretation and application of important sequential consecutive chemical processes, the implementation of sustainable fermentation methods, and potentially new avenues of drug research and discovery.
细菌与人体密切相关;有益的细菌通过帮助消化,防止感染和刺激免疫系统来支持健康和福祉。由细菌产生的物质,称为代谢物,作为分子信号定义细菌-宿主关系。为了通过揭示疾病治疗的新方向来潜在地有益于生活质量,我们的方法是彻底研究变异梭杆菌,这是一种通常在动物肠道中发现的细菌,可能导致肠道疾病的发生。 我们的研究项目还专注于与质谱相关的化学过程,质谱是一种分子首先被充电,然后在能量输入时被分解成碎片的技术。形成的特定碎片具有诊断性,为在各种情况下识别毒品、环境污染物和爆炸物提供了基础,并可得出具有广泛影响的结论(例如,在体育运动中使用违禁物质)。为了更深入地了解这些重要应用背后的基本原理,我们选择了模仿当前药物和候选药物结构的物质,并且可以在多个位置容纳电荷,增加它们以两种或更多种不同方式分解的可能性(即,碎片化途径)。随着我们的解释性发展,质谱将提供丰富和更可靠的信息,增加其作为药物代谢物表征的重要工具的价值,并缩短在开发有前景的新药中完成这一重要步骤所需的时间。 作为遗传学研究的补充,我们正在进行的化学研究已经证明了肠道细菌的代谢多样性,导致产生八种物质,其中一种可能具有意想不到的功能,作为一种分子信号,与肠道疾病有关。通过鉴定用于形成这些代谢物的途径,可以将厌氧菌中独特的代谢过程作为选择性代谢抑制剂的靶标进行评估,这是一种新的合理设计策略,用于产生有效对抗对当前抗生素治疗具有抗性的病原菌的新型抗生素的先导化合物。此外,排泄的三种细菌代谢物作为可持续的化学原料具有重要的实际应用,例如用于制造具有生物医学应用的生物可降解聚合物。 在这项申请中,要求资助进行两项看似不同的研究调查。然而,在我们的机械研究方法的路径阐明和研究的物质的性质的思想过程中的共性提供了显着的重叠。对于每一个,我们设计和合成探针来测试途径假设,使用稳定同位素标记的物质收集证据,并在逻辑上吸收证据,以提供每个途径的可靠描述。总的来说,我们解决了肠道细菌和人类宿主之间关系的基本问题,这是细菌和人类代谢交叉点上一个复杂且相对未开发的领域。我们的基础科学研究计划将为重要的连续连续化学过程的解释和应用,可持续发酵方法的实施以及药物研究和发现的潜在新途径提供新的见解。

项目成果

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White, Robert其他文献

Attachment-based psychosocial programme for under-privileged school children with adverse life experiences in Istanbul, Turkey.
  • DOI:
    10.1186/s40359-022-00938-x
  • 发表时间:
    2022-10-08
  • 期刊:
  • 影响因子:
    3.6
  • 作者:
    Warfa, Nasir;Bademci, Ozden;Karasar, Sahin;White, Robert
  • 通讯作者:
    White, Robert
Real world evidence (RWE) - a disruptive innovation or the quiet evolution of medical evidence generation?
  • DOI:
    10.12688/f1000research.13585.2
  • 发表时间:
    2018-01-01
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Khosla, Sajan;White, Robert;Leonard, Sandra
  • 通讯作者:
    Leonard, Sandra
A cis-regulatory map of the Drosophila genome.
  • DOI:
    10.1038/nature09990
  • 发表时间:
    2011-03-24
  • 期刊:
  • 影响因子:
    64.8
  • 作者:
    Negre, Nicolas;Brown, Christopher D.;Ma, Lijia;Bristow, Christopher Aaron;Miller, Steven W.;Wagner, Ulrich;Kheradpour, Pouya;Eaton, Matthew L.;Loriaux, Paul;Sealfon, Rachel;Li, Zirong;Ishii, Haruhiko;Spokony, Rebecca F.;Chen, Jia;Hwang, Lindsay;Cheng, Chao;Auburn, Richard P.;Davis, Melissa B.;Domanus, Marc;Shah, Parantu K.;Morrison, Carolyn A.;Zieba, Jennifer;Suchy, Sarah;Senderowicz, Lionel;Victorsen, Alec;Bild, Nicholas A.;Grundstad, A. Jason;Hanley, David;MacAlpine, David M.;Mannervik, Mattias;Venken, Koen;Bellen, Hugo;White, Robert;Gerstein, Mark;Russell, Steven;Grossman, Robert L.;Ren, Bing;Posakony, James W.;Kellis, Manolis;White, Kevin P.
  • 通讯作者:
    White, Kevin P.
Genome-Wide Analysis of the Binding of the Hox Protein Ultrabithorax and the Hox Cofactor Homothorax in Drosophila
  • DOI:
    10.1371/journal.pone.0014778
  • 发表时间:
    2011-04-05
  • 期刊:
  • 影响因子:
    3.7
  • 作者:
    Choo, Siew Woh;White, Robert;Russell, Steven
  • 通讯作者:
    Russell, Steven
A Longitudinal Linear Model of Patient Characteristics to Predict Failure to Attend an Inner-City Chronic Pain Clinic
  • DOI:
    10.1016/j.jpain.2014.03.004
  • 发表时间:
    2014-07-01
  • 期刊:
  • 影响因子:
    4
  • 作者:
    Shaparin, Naum;White, Robert;Kaufmann, Andrew
  • 通讯作者:
    Kaufmann, Andrew

White, Robert的其他文献

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{{ truncateString('White, Robert', 18)}}的其他基金

Elucidation of Pathways: Bacterial and Mass Spectrometric Studies
途径阐明:细菌和质谱研究
  • 批准号:
    RGPIN-2014-04536
  • 财政年份:
    2019
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Discovery Grants Program - Individual
Elucidation of Pathways: Bacterial and Mass Spectrometric Studies
途径阐明:细菌和质谱研究
  • 批准号:
    RGPIN-2014-04536
  • 财政年份:
    2017
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Discovery Grants Program - Individual
Elucidation of Pathways: Bacterial and Mass Spectrometric Studies
途径阐明:细菌和质谱研究
  • 批准号:
    RGPIN-2014-04536
  • 财政年份:
    2016
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Discovery Grants Program - Individual
Elucidation of Pathways: Bacterial and Mass Spectrometric Studies
途径阐明:细菌和质谱研究
  • 批准号:
    RGPIN-2014-04536
  • 财政年份:
    2015
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Discovery Grants Program - Individual
Elaboration of Differential Mobility Spectrometry using Isomeric Ions and Computational Chemistry
使用同分异构离子和计算化学详细阐述微分淌度谱测定法
  • 批准号:
    463703-2014
  • 财政年份:
    2014
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Engage Grants Program
Bioorganic chemistry
生物有机化学
  • 批准号:
    104262-2008
  • 财政年份:
    2012
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Discovery Grants Program - Individual
Bioorganic chemistry
生物有机化学
  • 批准号:
    104262-2008
  • 财政年份:
    2011
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Discovery Grants Program - Individual
Bioorganic chemistry
生物有机化学
  • 批准号:
    104262-2008
  • 财政年份:
    2010
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Discovery Grants Program - Individual
Bioorganic chemistry
生物有机化学
  • 批准号:
    104262-2008
  • 财政年份:
    2009
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Discovery Grants Program - Individual
Bioorganic chemistry
生物有机化学
  • 批准号:
    104262-2008
  • 财政年份:
    2008
  • 资助金额:
    $ 2.19万
  • 项目类别:
    Discovery Grants Program - Individual

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职业:剖析细胞通路和信号网络,协调植物防御反应及其与细菌毒力因子的相互作用
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Investigating essential pathways for the O-acetylation of the bacterial cell wall polymer peptidoglycan
研究细菌细胞壁聚合物肽聚糖 O-乙酰化的重要途径
  • 批准号:
    548044-2020
  • 财政年份:
    2022
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  • 批准号:
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细菌鞘脂 - 揭示宿主与微生物相互作用中关键参与者的隐藏生物合成途径。
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探索细菌细胞包膜的异质生物发生途径。
  • 批准号:
    2588441
  • 财政年份:
    2021
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  • 项目类别:
    Studentship
Structure and mechanism of bacterial DNA repair pathways
细菌DNA修复途径的结构和机制
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    2021
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  • 批准号:
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