Structural and functional characterization of the Thermotoga maritima Cmr complex
Structural and functional characterization of the Thermotoga maritima Cmr complex
批准号:
8709849
负责人:
Michael Anthony Estrella
金额:
$4.27万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-04-01 至 2016-03-31
关键词:
AddressAntimicrobial ResistanceArchitectureBacteriaBindingBiochemicalBiochemistryBiological AssayCatalytic DomainCleaved cellClustered Regularly Interspaced Short Palindromic RepeatsCodeComplexCrystallographyDNADataData SetDevelopmentGenetic MaterialsGenomeGoalsGuide RNAHealthHorizontal Gene TransferHumanImmuneImmune systemImmunityIn VitroIncubatedIndividualKineticsKnowledgeLengthMapsMethodsModelingMolecularMolecular Sieve ChromatographyMutation AnalysisNamesNucleic AcidsNucleotidesOrganismPathway interactionsPlasmidsProkaryotic CellsPropertyProtein SubunitsProteinsPublic Health Applications ResearchPublishingPyrococcus furiosusRNARNA InterferenceRNA-Induced Silencing ComplexRNA-Protein InteractionReactionReadingRecombinantsResistanceResolutionRoleRouteSet proteinSmall RNAStructural ModelsStructureSystemTechniquesTestingThermotoga maritimaThermus thermophilusTimeTranscriptUnited States National Institutes of HealthVirusbacterial resistancebasebiological systemsdisorder controlelectron densityexpectationgenetic elementimprovedin vivointerestnew technologynovelnucleaseprotein complexpublic health relevancereconstitutionresistance factorsstructural biology
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): In prokaryotes, clustered regularly interspaced short palindromic repeat (CRISPR) loci encode small CRISPR RNAs (crRNA) that protect against invasive genetic elements. These crRNAs are used as guides by various CRISPR associated (Cas) proteins to target foreign genetic elements and are the bases of a prokaryotic defense system that preserves the host genome. The Cas module RAMP (Cmr) proteins form a complex that is unique amongst the CRISPR/Cas systems for its ability to target and cleave RNA, whereas the other systems target DNA. The Cmr complex is composed of 6 protein subunits, named Cmr1-6, and a crRNA. Our goal is to understand the roles of the individual Cmr subunits and their interactions in the complex using biochemical and structural approaches. It is important to understand these fundamental properties of CRISPR/Cas complexes because of their central role in prokaryotic immunity and our lack of knowledge in this important pathway. Upon better understanding, we hope that manipulation of this natural pathway may be used to impair the spread of antimicrobial resistance factors. It has been demonstrated that the CRISPR/Cas system is able to limit horizontal gene transfer, which is the main route for bacteria to acquire resistance, by targeting the degradation of conjugative plasmids. A role can be conceived whereby specifically Cmr can be used silence RNA transcripts that may code for proteins that facilitate HGT. Such developments may have considerable public health applications and would be consistent with the NIH goals of advancing our understanding of biological systems, controlling disease and improving human health.
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Structural and functional characterization of the Thermotoga maritima Cmr complex
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批准号:8459153
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项目类别:
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资助金额:$4.22万
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财政年份:2013
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负责人:Michael Anthony Estrella
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依托单位:
Structural and functional characterization of the Thermotoga maritima Cmr complex
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批准号:8821632
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项目类别:
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资助金额:$4.31万
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财政年份:2013
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负责人:Michael Anthony Estrella
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依托单位:
海外基金