课题基金 / 基金详情

PROTEIN-NO INTERACTIONS PROBED BY CONVENTIONAL AND TIME-RESOLVED X-RAY CRYSTA

PROTEIN-NO INTERACTIONS PROBED BY CONVENTIONAL AND TIME-RESOLVED X-RAY CRYSTA
通过传统和时间分辨 X 射线晶体探测蛋白质-无相互作用
批准号:
7956815
负责人:
MARIUS SCHMIDT
金额:
$0.47万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-08-01 至 2010-07-31

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中文摘要
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英文摘要
This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Since the late 80s nitric oxide has been recognized to have many important physiological roles. For example, NO has important signaling functions, and is a potent antimicrobial agent active against a wide range of bacteria, viruses, fungi and even parasites. Nitric oxide?s physiological functions almost invariably involve specific interactions with proteins; much progress has been made in identifying the mechanisms of such protein-NO interactions, but many questions remain. Herein we propose to develop broadly applicable methodologies for photochemically generating free NO within a protein crystal, so that subsequent interactions of NO with the protein can be monitored in real time using time-resolved protein X-ray crystallography. Such methodologies will be invaluable tools for studying the detailed mechanisms of NO signaling and antimicrobial phenomena. The project will be divided into 2 phases. In phase 1 various methods for NO photogeneration will be tested on crystals of bovine liver catalase and superoxide dismutase (SOD) from Propionibacterium shermanii. Both are readily available proteins whose crystal structures are known, and that interact strongly with NO. In the second phase of the project the best NO photogenerating systems will be used to investigate NO interaction with oxygenated HbN from M. tuberculosis. HbN is a protein that is thought to protect M. tuberculosis from the body?s defenses, and allow TB to persist for years in a latent state. The aim of this phase will be to show that our method can be applied to a system of considerable importance in medicine and public health.
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5-D CRYSTALLOGRAPHY SPACE TIME AND TEMPERATURE
  • 批准号:
    8363671
  • 项目类别:
  • 资助金额:
    $8.52万
  • 财政年份:
    2011
  • 负责人:
    MARIUS SCHMIDT
  • 依托单位:
PROTEIN-NO INTERACTIONS PROBED BY CONVENTIONAL AND TIME-RESOLVED X-RAY CRYSTA
  • 批准号:
    8363698
  • 项目类别:
  • 资助金额:
    $3.65万
  • 财政年份:
    2011
  • 负责人:
    MARIUS SCHMIDT
  • 依托单位:
5-D CRYSTALLOGRAPHY, SPACE, TIME AND TEMPERATURE
  • 批准号:
    8171971
  • 项目类别:
  • 资助金额:
    $0.73万
  • 财政年份:
    2010
  • 负责人:
    MARIUS SCHMIDT
  • 依托单位:
PROTEIN-NO INTERACTIONS PROBED BY CONVENTIONAL AND TIME-RESOLVED X-RAY CRYSTA
  • 批准号:
    8171972
  • 项目类别:
  • 资助金额:
    $2.8万
  • 财政年份:
    2010
  • 负责人:
    MARIUS SCHMIDT
  • 依托单位:
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