Molecular Screening Shared Resouce
分子筛选共享资源
基本信息
- 批准号:7944609
- 负责人:
- 金额:$ 14.96万
- 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
- 起止时间:2009-04-02 至 2013-11-30
- 项目状态:已结题
- 来源:
- 关键词:Animal ModelAreaBiochemicalBiologicalBiological AssayBudgetsCaliforniaCancer CenterCancer Center Support GrantCell Culture TechniquesCellular biologyCharacteristicsCommunity Clinical Oncology ProgramConsultationsDevelopmentEquipmentFundingGene Expression RegulationGenitourinary systemHematopoietic NeoplasmsHumanIncubatorsIndividualInstitutesInstructionJonsson Comprehensive Cancer Center of University of California Los AngelesKnock-outLeadershipLettersLibrariesMolecularMolecular EpidemiologyMusProteinsRNA SequencesRNA libraryReaderRecording of previous eventsReportingResource SharingResourcesRoboticsRunningScienceScreening procedureSignal TransductionTechnologyTherapeuticThoracic OncologyUnited States National Institutes of HealthValidationYeastsZebrafishcancer cellcarcinogenesiscollegefollow-upgenome sequencinggenome wide association studygenome-widehigh throughput screeningmedical schoolsmeetingsmembernanosystemsprogramssmall moleculesmall molecule librariestumor immunology
项目摘要
The Molecular Screening Shared Resource (MSSR): Completion of the genome sequences of humans,
mice, zebrafish and a number of other model organisms has led to the tentative identification of all encoded
proteins in these species. The proliferation both of chemical libraries and of libraries of genome wide
inhibitory RNA sequences for a number of species has made it possible to conceive of looking for inhibitory
small molecules and inhibitory RNAs for all genetically encoded targets. The concomitant development of
High Throughput Screening (NTS) technologies has made it possible - with the right resources - to move
this from concept to practice. The UCLA JCCC Molecular Screening Shared Resource (MSSR) was
established in 2003 to meet this exciting scientific objective. The MSSR now has dedicated space in the
new California NanoSystems Institute, small molecule libraries containing over 70,000 compounds, genomewide
knockout libraries for yeast, and interfering RNA libraries for both murine and human targets. Excellent
academic and technical leadership has established a robust, accessible screening center that assists both in
developing reliable and robust enzymatic and cell culture HTS assays and in facilitating genome-wide
screens. The David Geffen School of Medicine, the California NanoSystems Institute (CNSI), the UCLA
College of Letters and Science, several individual departments and some private donors have joined the
JCCC to provide funding for the equipment and libraries (well over $1,000,000) and operating "start-up"
required to get the MSSR up and running. The Shared Resource has run (or is currently running) 65
screens, the great majority of which are for JCCC members. Members of the Gene Regulation, Signal
Transduction and Therapeutics, Tumor Immunology, Cancer Cell Biology, Hematopoietic Malignancies,
Developing Program in Molecular Epidemiology and Carcinogenesis, Thoracic Oncology and Genitourinary
Oncology Program Areas have already utilized this Shared Resource. The CCSG budget request for this
Shared Resource for the first year CCSG budget is for 13% of the estimated operating budget; support for
the shared resource also comes from the CNSI, an NIH Center for Radioprotectors, the UCLA Chancellor's
Biosciences Initiative, user recharges and philanthropy. (Please also see Section 6.2.3 on Shared
Resources in the History, Description, Essential Characteristics).
Eight Cancer Center members representing four Cancer Center Program Areas completed screens in
the Molecular Screening Shared Resource during the reporting period; many screens are ongoing.
This is a continuing shared resource.
分子筛选共享资源 (MSSR):完成人类基因组序列,
小鼠、斑马鱼和许多其他模式生物已导致所有编码的初步鉴定
这些物种中的蛋白质。化学文库和全基因组文库的增殖
许多物种的抑制性RNA序列使得寻找抑制性RNA成为可能
针对所有基因编码靶标的小分子和抑制性 RNA。随之而来的发展
高通量筛选 (NTS) 技术使得在适当的资源下移动成为可能
这是从概念到实践。加州大学洛杉矶分校 JCCC 分子筛选共享资源 (MSSR)
成立于 2003 年,旨在实现这一令人兴奋的科学目标。 MSSR 现在在
新的加州纳米系统研究所,包含超过 70,000 种全基因组化合物的小分子库
酵母的敲除文库,以及鼠类和人类靶标的干扰 RNA 文库。出色的
学术和技术领导层建立了一个强大的、易于使用的筛选中心,协助
开发可靠且强大的酶和细胞培养 HTS 测定并促进全基因组
屏幕。大卫格芬医学院、加州纳米系统研究所 (CNSI)、加州大学洛杉矶分校
文学与科学学院、几个单独的院系和一些私人捐助者已加入
JCCC 将为设备和图书馆提供资金(远超过 1,000,000 美元)和运营“启动”
启动并运行 MSSR 所需的。共享资源已运行(或当前正在运行) 65
屏幕,其中绝大多数是为 JCCC 会员提供的。基因调控、信号成员
转导和治疗、肿瘤免疫学、癌细胞生物学、造血系统恶性肿瘤、
分子流行病学和癌变、胸部肿瘤学和泌尿生殖学发展项目
肿瘤学计划领域已经利用了该共享资源。 CCSG 对此的预算请求
CCSG 第一年的共享资源预算占预计运营预算的 13%;支持
共享资源还来自 CNSI、NIH 辐射防护中心、加州大学洛杉矶分校校长的
生物科学倡议、用户充值和慈善事业。 (另请参阅第 6.2.3 节“共享”
历史、描述、基本特征中的资源)。
代表四个癌症中心项目领域的八名癌症中心成员完成了筛选
报告期内的分子筛选共享资源;许多屏幕正在进行中。
这是一个持续的共享资源。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Kenneth Alan Bradley其他文献
Kenneth Alan Bradley的其他文献
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{{ truncateString('Kenneth Alan Bradley', 18)}}的其他基金
Cellular Intoxication Pathway of Cytolethal Distending Toxin
细胞致死膨胀毒素的细胞中毒途径
- 批准号:
8322033 - 财政年份:2011
- 资助金额:
$ 14.96万 - 项目类别:
Cellular Intoxication Pathway of Cytolethal Distending Toxin
细胞致死膨胀毒素的细胞中毒途径
- 批准号:
8163122 - 财政年份:2011
- 资助金额:
$ 14.96万 - 项目类别:
Cellular Intoxication Pathway of Cytolethal Distending Toxin
细胞致死膨胀毒素的细胞中毒途径
- 批准号:
8730187 - 财政年份:2011
- 资助金额:
$ 14.96万 - 项目类别:
Cellular Intoxication Pathway of Cytolethal Distending Toxin
细胞致死膨胀毒素的细胞中毒途径
- 批准号:
8607690 - 财政年份:2011
- 资助金额:
$ 14.96万 - 项目类别:
Cellular Intoxication Pathway of Cytolethal Distending Toxin
细胞致死膨胀毒素的细胞中毒途径
- 批准号:
8536865 - 财政年份:2011
- 资助金额:
$ 14.96万 - 项目类别:
Retrocyclins: Cyclic mini-defensins that inactivate anthrax toxins
逆转录素:可灭活炭疽毒素的环状迷你防御素
- 批准号:
7463962 - 财政年份:2009
- 资助金额:
$ 14.96万 - 项目类别:
Genetics Modifiers of Anthrax Lethal Toxin Induced Pathophysiology
炭疽致死毒素诱导病理生理学的遗传学修饰
- 批准号:
7590997 - 财政年份:2009
- 资助金额:
$ 14.96万 - 项目类别:
Genetics Modifiers of Anthrax Lethal Toxin Induced Pathophysiology
炭疽致死毒素诱导病理生理学的遗传学修饰
- 批准号:
7895640 - 财政年份:2009
- 资助金额:
$ 14.96万 - 项目类别:
Retrocyclins: Cyclic mini-defensins that inactivate anthrax toxins
逆转录素:可灭活炭疽毒素的环状迷你防御素
- 批准号:
7897621 - 财政年份:2009
- 资助金额:
$ 14.96万 - 项目类别:
Genetics Modifiers of Anthrax Lethal Toxin Induced Pathophysiology
炭疽致死毒素诱导病理生理学的遗传学修饰
- 批准号:
7690580 - 财政年份:2008
- 资助金额:
$ 14.96万 - 项目类别:
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