A Novel Computational Package for DNA Enzyme Design
A Novel Computational Package for DNA Enzyme Design
批准号:
7799782
负责人:
Jingdong Tian
金额:
$19.31万
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:
2009-04-03 至 2011-06-30
关键词:
Activities of Daily LivingAddressAlgorithmsAmino AcidsAreaArtsBackBiologicalBiological ModelsBiomedical ComputingBiotechnologyCatalogingCatalogsCleaved cellClinicalCodon NucleotidesComplexComputer softwareCustomDNADNA PackagingDNA Restriction EnzymesDNA SequenceDNA-Protein InteractionDatabasesDeoxyribonuclease IDevelopmentEngineeringEnzyme InteractionEnzymesExhibitsFutureGenerationsGenomeGoalsHuman GenomeImageryInvestigationLibrariesLifeMaintenanceMolecular ConformationMolecular ModelsMutationNucleic AcidsNucleotidesOrganismOutcomePartner in relationshipPerformancePositioning AttributeProcessRecombinantsResearchRetrievalSchemeScreening procedureSideSiteSite-Directed MutagenesisSpecificityStructural ModelsStructureSugar PhosphatesTechnologyTherapeuticTimeTranslatingTranslational ResearchValidationVertebral columnbasecomputerized toolscostdesignendonucleaseengineering designgene synthesisimprovedinnovationinsightinterestinterfacialmolecular modelingnanomedicinenovelprotein expressionrestriction enzymescaffoldstructural biologytoolweb-enabled
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): In the area of enzyme design and engineering, DNA restriction endonucleases (REs) are of particular interest and present compelling challenges. Restriction enzymes recognize short defined DNA sequences and cleave the DNA sugar-phosphate backbone with considerable efficiency. These enzymes have been studied for over half a century and have given rise to the era of recombinant biotechnology in the past few decades. Yet, their structural features and propensities that lend their functional ability to recognize short DNA sequences in the genome have yet to be understood at predictive proficiency. The general goal of this research is to develop a computational tool to enable study and reengineering of DNA restriction enzymes. The package will include the following components: 1) nucleic acid recognition site perturbation tools, which will allow sequence recognition, structural modeling and visualization of the nucleic acid recognition site; 2) a biological focusing algorithm which will enumerate and focus on those scaffolds and interfacial pockets (IPs) that have potential for design, as demonstrated by evolutionarily favorable features; and 3) a DNA endonuclease library integration and querying interface which will streamline the cataloging, retrieval, use, and dissemination of analyses performed using the above tools and algorithm. These computational tools, once developed, will help launch systemic research into the fundamentals of structural biology and engineering of restriction endonucleases. The development of such innovative biomedical computing technologies will be facilitated by the research group's strength in high-performance molecular modeling and optimization as well as high-throughput gene synthesis, protein expression, and screening technologies. This research will eventually translate into custom-designed endonucleases for sequence-specific biomolecular probes or clinical therapeutic in further investigations or treatments.
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Automated long DNA synthesis technology
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批准号:8268351
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项目类别:
-
资助金额:$38.27万
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财政年份:2011
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负责人:Jingdong Tian
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依托单位:
Automated long DNA synthesis technology
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批准号:8451452
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项目类别:
-
资助金额:$36.51万
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财政年份:2011
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负责人:Jingdong Tian
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依托单位:
Automated long DNA synthesis technology
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批准号:8051453
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项目类别:
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资助金额:$38.31万
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财政年份:2011
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负责人:Jingdong Tian
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依托单位:
A Novel Computational Package for DNA Enzyme Design
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批准号:7661170
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项目类别:
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资助金额:$23.4万
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财政年份:2009
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负责人:Jingdong Tian
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依托单位:
海外基金