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The Institute for Biomolecular Targeting

The Institute for Biomolecular Targeting
生物分子靶向研究所
批准号:
10647696
负责人:
DEAN R MADDEN
金额:
$246.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
未结题
起止时间:
2016-05-15 至 2026-05-31
关键词:
2019-nCoVAccelerationAddressAntibodiesAreaAutophagocytosisAwardAwarenessBindingBiologicalBusinessesCareer MobilityCenters of Research ExcellenceCommunitiesComplexConsultationsCore FacilityCryoelectron MicroscopyCystic FibrosisDedicationsDevelopmentDiabetes MellitusDiseaseDisparateDrug TargetingExtramural ActivitiesFacultyFaculty RecruitmentFinancial SupportFosteringFoundationsFundingFutureGenerationsGoalsGrantHomeImageImmunologicsInfectionInfrastructureInstitutionInvestigationInvestmentsIon ChannelMalignant NeoplasmsMass Spectrum AnalysisMembrane FusionMentorsMetabolic ControlMicroscopeMicroscopyModelingMolecularMolecular TargetNeoplasm MetastasisPathologyPhasePlayPostdoctoral FellowProductionProductivityProgram ReviewsProtein BiochemistryProteinsRecoveryResearchResearch InstituteResearch PersonnelResearch Project GrantsResourcesRespiratory Tract InfectionsRoleSchoolsScientistSeasonsSeriesServicesSignal TransductionSubgroupTargeted ResearchTeacher Professional DevelopmentTechnologyTestingTherapeuticTimeTranslationsVaccinesVirus DiseasesWorkcareerclinical practicecohortcommunity buildingcostdiversity and inclusiondrug developmentexperiencefaculty researchfaculty supportfascinateforgingfundamental researchinnovationinstrumentinstrumentationinterestknowledge translationmembermid-career facultymolecular imagingnew technologynovel therapeutic interventionoperationpre-clinicalpreclinical developmentprogramsprotein expressionrecruitsuccesssymposiumtherapeutic targettooltranslational goaltumor progression

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中文摘要
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英文摘要
The Dartmouth Institute for Biomolecular Targeting (bioMT) infuses mechanistic investigations with a sophisticated awareness of disease pathology and therapeutic need, enhancing the quality of even the most fundamental research. At the same time, it helps orient mechanistic investigations towards long-term translational goals for complex diseases such as cancer and infections. In phase I, our progress was strong. All six of our research project leaders (RPL) with more than two years’ support have received R01-equivalent funding. Our cores provide unique protein biochemistry resources and ‘navigators’ to access microscopes campus-wide. Our cores and seminars have created a vibrant and interdisciplinary community. Here, we propose to deploy phase II COBRE and institutional program enrichment funds to build on this foundation and fill key gaps to prepare bioMT for the transition to sustainable COBRE independence. Aim 1 is to increase our cohort of funded bioMT investigators to fill strategic roles in our research landscape. Our two most recent RPLs (3–15 months’ support) are continuing into phase II, joined by two outstanding new hires. Their projects explore basic signaling and immunological mechanisms with potential relevance to therapeutic targets ranging from respiratory infections to cancer progression and metastasis, interconnected by shared scientific and technical interests. All receive guidance from dedicated mentoring dyads to assist in career advancement and independent extramural funding, and all receive support from responsive scientific cores offering state-of-the- art technologies directly relevant to their bioMT research projects. With institutional support, we will also hire five new faculty members, aligned with our theme of discovering and exploiting molecular targets, and selected to enhance thematic subgroups. As starting RPLs graduate, we will recruit new hires and other potential candidates for EAC consideration as replacements. Aim 2 is to enhance our core facilities and prepare them for a transition to COBRE independence during phase III. The cores are fully staffed and have invested heavily in phase I instrumentation. We will partner to add key new technologies based on user input, including parallel protein expression, mass spectrometry, advanced microscopy, and cryoEM. Cost-recovery models will be developed for incremental deployment in phase III to enable core financial independence. Aim 3 continues enriching our community, including mini-symposia and pilot awards to foster new multi-PI and program-project applications, which will contribute to core sustainability. Overall, these aims will leverage proven COBRE strategies – junior faculty hiring, extramural and academic mentoring, excellent administrative and scientific core support, and interdisciplinary community building – to enhance bioMT’s scientific impact in targeted areas of need. This will prepare us for the transition to phase III funding and ultimate independence as an interdisciplinary and nationally visible research institute, spanning three schools and 10 departments at Dartmouth and deeply connected to local centers and regional IDeA partners.
期刊论文(91)
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DOI: 10.1128/mbio.01493-21
发表时间: 2021-06-29
期刊: mBio
影响因子: 6.4
作者: [Wang B, Zhou X, Gerber SA, Loros JJ, Dunlap JC]
通讯作者: Dunlap JC
DOI: 10.1016/j.jneumeth.2021.109437
发表时间: 2022-02-01
期刊: Journal of neuroscience methods
影响因子: 3
作者: [De La Torre AL, Smith C, Granger J, Anderson FL, Harned TC, Havrda MC, Chang CCY, Chang TY]
通讯作者: Chang TY
Influence of the Interdomain Interface on Structural and Redox Properties of Multiheme Proteins.
域间界面对多血红素蛋白结构和氧化还原性质的影响。
DOI: 10.1021/acs.inorgchem.2c03427
发表时间: 2022
期刊: Inorganic chemistry
影响因子: 4.6
作者: [Zhong,Fangfang, Albert,Therese, Moënne-Loccoz,Pierre, Pletneva,EkaterinaV]
通讯作者: Pletneva,EkaterinaV
Publisher Correction: An engineered human Fc domain that behaves like a pH-toggle switch for ultra-long circulation persistence.
出版商更正:一种工程化的人类 Fc 结构域,其行为类似于 pH 切换开关,可实现超长的循环持久性。
DOI: 10.1038/s41467-019-13458-x
发表时间: 2019
期刊: Nature communications
影响因子: 16.6
作者: [Lee,Chang-Han, Kang,TaeHyun, Godon,Ophélie, Watanabe,Makiko, Delidakis,George, Gillis,CaitlinM, Sterlin,Delphine, Hardy,David, Cogné,Michel, Macdonald,LynnE, Murphy,AndrewJ, Tu,Naxin, Lee,Jiwon, McDaniel,JonathanR, Makowski,Emily, Tess]
通讯作者: Tess
55
    DartCF: The Dartmouth Cystic Fibrosis Research Center
    • 批准号:
      10686303
    • 项目类别:
    • 资助金额:
      $120.82万
    • 财政年份:
      2018
    • 负责人:
      DEAN R MADDEN
    • 依托单位:
    Enrichment and Research Administration Core
    • 批准号:
      10686304
    • 项目类别:
    • 资助金额:
      $21.04万
    • 财政年份:
      2018
    • 负责人:
      DEAN R MADDEN
    • 依托单位:
    DartCF: The Dartmouth Cystic Fibrosis Research Center
    • 批准号:
      10895149
    • 项目类别:
    • 资助金额:
      $47.11万
    • 财政年份:
      2018
    • 负责人:
      DEAN R MADDEN
    • 依托单位:
    DartCF: The Dartmouth Cystic Fibrosis Research Center
    • 批准号:
      10001759
    • 项目类别:
    • 资助金额:
      $122.42万
    • 财政年份:
      2018
    • 负责人:
      DEAN R MADDEN
    • 依托单位:
    海外基金