Development of high-dose time-resolved X-ray footprinting technologies to enable detailed structural and kinetics information to be obtained for challenging biological problems
Development of high-dose time-resolved X-ray footprinting technologies to enable detailed structural and kinetics information to be obtained for challenging biological problems
批准号:
10630950
负责人:
CORIE Y RALSTON
金额:
$42.45万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
未结题
起止时间:
2018-01-01 至 2026-05-31
关键词:
AntibodiesAwardBindingBiologicalBiomedical ResearchBlood capillariesCellsCollectionCommunitiesComplexCountryDataData CollectionDevelopmentDoseDose RateDrynessEnvironmentExclusionExposure toFingerprintFluorescenceFluorescence SpectroscopyFundingGoalsGrantHybridsInjectionsInvestigationKineticsLightLiquid substanceLocationMapsMass Spectrum AnalysisMeasurementMembrane ProteinsMethodologyMethodsMicrofluidicsMolecular ConformationProtein DynamicsProteinsPumpRaman Spectrum AnalysisResearchResearch PersonnelResolutionRoentgen RaysSamplingSolventsSourceSpectrum AnalysisSpeedStructureSynchrotronsSystemTechnologyTimeTubeWaterX ray spectroscopybeamlinebiological systemsbiophysical techniquesbiophysical toolschromophoredata qualitydetectorexperimental studyflexibilityimprovedinsightinstrumentinstrumentationmacromolecular assemblymacromoleculenovelprotein complexprotein structuresmall moleculestructural biologysuccesstool
中文摘要
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英文摘要
Abstract
The overarching goal in this project, both in the funded award and in this renewal, is to advance the
structural biology method of X-ray footprinting mass spectrometry (XFMS) in capability and accessibility
such that it becomes a premiere biophysical tool for biomedical investigators around the country. XFMS
is a solution state method used to map solvent accessible regions in macromolecules on a timescale of
microseconds, yielding information on conformation, protein-protein dynamics, and bound water
location and dynamics. It has been used to obtain useful structural information on a diverse range
biological systems, from small proteins to large complexes, as well as membrane proteins, and for
mapping interaction regions in antibody-target complexes. As part of the original award, we made
substantial progress towards our main goal by developing a unique high-throughput and automated
XFMS instrument, enabling use of the method to researchers nationwide. In this proposed renewal, we
plan to build on this success to implement new capabilities in keeping with the original goal of the grant.
Specifically, we plan to integrate fluorescence and Raman spectroscopies, fast mixing with jet delivery
capability, and size exclusion directly inline with the XFMS instrument. The integration of these
technologies into the XFMS instrument will enable even more challenging biological systems to be
studied using the method. While the new specific aims are ambitious, they build naturally from our
proven track record in developing complex instrumentation and the successful research team we built
during the first grant period. Proof of principle for these technologies is presented, along with
preliminary data, and the proposal outlines the significant technical challenges involved and how they
will be overcome. The resulting technologies will be a significant gain to the biomedical research
community and will be used to meet the increasing demand for access to the XFMS method.
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CcmK3 和 CcmK4 形成的异六聚体增加了 Beta 羧基体壳的复杂性。
DOI:
10.1104/pp.18.01190
发表时间:
2019
期刊:
Plant physiology
影响因子:
7.4
作者:
[Sommer,Manuel, Sutter,Markus, Gupta,Sayan, Kirst,Henning, Turmo,Aiko, Lechno-Yossef,Sigal, Burton,RodneyL, Saechao,Christine, Sloan,NancyB, Cheng,Xiaolin, Chan,Leanne-JadeG, Petzold,ChristopherJ, Fuentes-Cabrera,Miguel, Ralston,CorieY, ]
通讯作者:
DOI:
10.1038/s41467-018-06034-2
发表时间:
2018-08-30
期刊:
Nature communications
影响因子:
16.6
作者:
[Huang W, Peng Y, Kiselar J, Zhao X, Albaqami A, Mendez D, Chen Y, Chakravarthy S, Gupta S, Ralston C, Kao HY, Chance MR, Yang S]
通讯作者:
Yang S
DOI:
10.1038/s42003-022-03775-1
发表时间:
2022-08-25
期刊:
Communications biology
影响因子:
5.9
作者:
[]
通讯作者:
DOI:
10.1038/s41598-020-72383-y
发表时间:
2020-09-23
期刊:
Scientific reports
影响因子:
4.6
作者:
[Dominguez-Martin MA, Hammel M, Gupta S, Lechno-Yossef S, Sutter M, Rosenberg DJ, Chen Y, Petzold CJ, Ralston CY, Polívka T, Kerfeld CA]
通讯作者:
Kerfeld CA
DOI:
10.1016/j.bbapap.2020.140562
发表时间:
2021-03
期刊:
Biochimica et biophysica acta. Proteins and proteomics
影响因子:
--
作者:
[Sevillano N, Bohn MF, Zimanyi M, Chen Y, Petzold C, Gupta S, Ralston CY, Craik CS]
通讯作者:
Craik CS
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STRUCTURE OF TWO NIFE CLUSTERS IN CODH FROM CLOSTRIDIUM THERMOACETICUM
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财政年份:--
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负责人:CORIE Y RALSTON
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依托单位:--
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