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Acquisition of a Pulse Electron Paramagnetic Resonance Spectrometer

Acquisition of a Pulse Electron Paramagnetic Resonance Spectrometer
脉冲电子顺磁共振波谱仪的采集
批准号:
7840304
负责人:
Peter Z Qin
金额:
$103.99万
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:
2009-12-07 至 2011-12-06

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The bio-molecular research community in the Los Angeles area is requesting NIH funding to purchase a state-of-art pulse electron paramagnetic resonance (EPR) spectrometer, the EleXsys FT-EPR system from Bruker Corporation. Pulse EPR spectroscopy is a powerful tool for analyzing conformations and metal ion cofactors of biological systems. The proposed pulse EPR spectrometer simultaneously will provide two capabilities that are central to the participating users. One is Double Electron Electron Resonance (DEER) spectroscopy, which selectively measures electron spin dipolar interactions to yield inter-spin distances up to 80 ¿ in bio-molecules. The measured distances provide direct structural constraints for mapping global structures and monitoring conformational changes of complex bio-molecular systems. User projects that require DEER span many important public health related areas, including viral replication and infection (X. Chen, Goodman, Qin), protein trafficking (Shan), transcription regulation (L. Chen), and human chromosomal translocation (Lieber). The second type of pulse EPR measurement is Electron Nuclear Double Resonance (ENDOR) and Electron Spin Echo Envelope Modulation (ESEEM), which measure interactions between the electron spin and the surrounding nuclei. This will be used to study ligand identity and coordination geometry of metal co-factors in nitrogenase (Rees, McKenna), DNA polymerase (McKenna, Crans, Goodman), and amoyloid formation in Alzheimer's disease (Zhou). Pulse EPR capabilities are grossly inadequate at the participating institutions. Funding of the proposed instrument will significantly benefit on-going research in the group of users, which are currently supported by 23 NIH grants. It will also support the broader regional research community, training of minorities, and educational missions. The award will immediately impact approximately 500 jobs in American, thus stimulating the economy.
期刊论文(6)
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会议论文
CRISPR-Cas9 Mediated DNA Unwinding Detected Using Site-Directed Spin Labeling.
使用定点自旋标记检测 CRISPR-Cas9 介导的 DNA 解旋。
DOI: 10.1021/acschembio.6b01137
发表时间: 2017
期刊: ACS chemical biology
影响因子: 4
作者: [Tangprasertchai,NarinS, DiFelice,Rosa, Zhang,Xiaojun, Slaymaker,IanM, VazquezReyes,Carolina, Jiang,Wei, Rohs,Remo, Qin,PeterZ]
通讯作者: Qin,PeterZ
Posttranscriptional site-directed spin labeling of large RNAs with an unnatural base pair system under non-denaturing conditions.
非变性条件下使用非天然碱基对系统对大 RNA 进行转录后定点自旋标记
DOI: 10.1039/d0sc01717e
发表时间: 2020-09-21
期刊: Chemical science
影响因子: 8.4
作者: [Wang Y, Kathiresan V, Chen Y, Hu Y, Jiang W, Bai G, Liu G, Qin PZ, Fang X]
通讯作者: Fang X
DOI: 10.1039/c3cc49575b
发表时间: 2014-03
期刊: Chemical communications
影响因子: 4.9
作者: [Sean P. Culver;V. Stepanov;Matthew Mecklenburg;Susumu Takahashi;R. Brutchey]
通讯作者: Sean P. Culver;V. Stepanov;Matthew Mecklenburg;Susumu Takahashi;R. Brutchey
DOI: 10.1021/acs.biochem.5b01189
发表时间: 2016-01-19
期刊: Biochemistry
影响因子: 2.9
作者: [Zhang X, Xu CX, Di Felice R, Sponer J, Islam B, Stadlbauer P, Ding Y, Mao L, Mao ZW, Qin PZ]
通讯作者: Qin PZ
Elucidating the Role of DNA Shape in CRISPR Target Discrimination
Elucidating the Role of DNA Shape in CRISPR Target Discrimination
Investigating mechanisms of DNA unwinding and recognition by a CRISPR-Cas nuclease
Supplement: Acquisition of a Multi-Mode Microplate Reader
国内基金
海外基金
新型F-18标记香豆素衍生物PET探针的研制及靶向Alzheimer's Disease 斑块显像研究
  • 批准号:
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  • 项目类别:
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  • 资助金额:
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  • 批准年份:
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  • 负责人:
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  • 依托单位:
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  • 项目类别:
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  • 资助金额:
    26.0万元
  • 批准年份:
    2010
  • 负责人:
    郭亚芬
  • 依托单位:
跨膜转运蛋白21(TMP21)对引起阿尔茨海默病(Alzheimer'S Disease)的γ分泌酶的作用研究