Purchase of an Echo 650 acoustic liquid handler with Access workstation
购买带有 Access 工作站的 Echo 650 声学液体处理机
基本信息
- 批准号:10176267
- 负责人:
- 金额:$ 56.67万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-07-01 至 2022-06-30
- 项目状态:已结题
- 来源:
- 关键词:Academic supportAcousticsAgingBiochemicalBiological AssayCancer Center Support GrantCellsDataDecision MakingDevelopmentDrug IndustryGrantGrant ReviewInfrastructureLiquid substanceMiniaturizationMinorMolecularPhiladelphiaPrincipal InvestigatorResearchResearch PersonnelSourceStructure-Activity RelationshipTechnologyThe Wistar InstituteUnited States National Institutes of Healthbasecostdrug discoveryexperiencehigh throughput screeningimprovedinstrumentminiaturizenanolitrenovelprotein expressionrecruitscreeningsmall moleculesound
项目摘要
PROJECT SUMMARY
Support is requested for the purchase of an Echo 650 acoustic liquid handler with Access workstation
to replace the Janus NanoHead, the existing and aging low volume liquid handler purchased in 2008 within the
Molecular Screening and Protein Expression Facility at The Wistar Institute in Philadelphia. This instrument
upgrade is critical for the Facility to continue to provide state-of-the-art support for the development of robust,
high-throughput biochemical and cell-based assays required for drug discovery. Indeed, Wistar has made a
commitment to academic drug discovery by recruiting its first medicinal chemist, Dr. Joseph M. Salvino, who is
the Principal Investigator of this application. Dr. Salvino and nine other major and minor users who hold a
combined 17 unique NIH grants (R01/R35/R61/P01/UM1/U54/DP2) have requested the Echo 650 with Access
workstation to develop improved biochemical and cell-based assays that generate better data which will enable
more informed decision making regarding novel structure-activity relationships. There are currently no similar
instruments that are accessible to Wistar investigators.
The Echo 650 is a highly accurate, low volume, non-contact liquid handler that moves nanoliter
volumes of liquid from one microplate to another using sound waves. Using direct dilution, it can determine the
potencies of small molecules with better precision as opposed to traditional serial dilution. The miniaturization
of such assays also reduces research costs. The Access workstation is the stacker unit integrated with the
Echo 650 which allows for automated plate handling necessary for high-throughput screening and hit picking of
active compounds. Because there is no contact between source plates, this technology eliminates compound
carry-over and protects the integrity of existing compounds in storage plates. The preliminary data described
in this application demonstrate that the Echo 650 is a superior technology to our existing Janus Nanohead. In
addition, we also show that we have the necessary infrastructure to miniaturize our assays to 1536-well format.
This instrument will significantly upgrade our capabilities regarding assay miniaturization while simultaneously
increasing the quality of our data.
The unit will be housed in the Molecular Screening and Protein Expression Facility, overseen by Dr.
Salvino and managed by Mr. Joel Cassel. Both Dr. Salvino and Mr. Cassel have over 40 years aggregate
experience in the pharmaceutical industry. The facility is well regarded and cumulatively ranked with a score
of “Exceptional” at the 2018 NIH/NCI Cancer Center support Grant (CCSG) review. We are seeking to
upgrade our existing low volume liquid handling technology to a superior state of the art, non-contact nanoliter
liquid handling technology in the Echo 650 with Access workstation in order to optimally support the academic
drug discovery initiatives of The Wistar Institute.
项目总结
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Thorectidiol A Isolated from the Marine Sponge Dactylospongia elegans Disrupts Interactions of the SARS-CoV-2 Spike Receptor Binding Domain with the Host ACE2 Receptor.
从海洋海绵 Dactylospongia elegans 中分离出来的 Thorectidiol A 可破坏 SARS-CoV-2 刺突受体结合域与宿主 ACE2 受体的相互作用。
- DOI:10.1021/acs.jnatprod.2c01030
- 发表时间:2023
- 期刊:
- 影响因子:5.1
- 作者:Williams,DavidE;Cassel,Joel;Zhu,Jin-Lin;Yang,Jian-Xiong;deVoogd,NicoleJ;Matainaho,Teatulohi;Salvino,JosephM;Wang,YanAlexander;Montaner,LuisJ;Tietjen,Ian;Andersen,RaymondJ
- 通讯作者:Andersen,RaymondJ
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Joseph M Salvino其他文献
Joseph M Salvino的其他文献
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{{ truncateString('Joseph M Salvino', 18)}}的其他基金
In Vivo Study of of Chemokine Antagonists for Cancer
癌症趋化因子拮抗剂的体内研究
- 批准号:
8690420 - 财政年份:2014
- 资助金额:
$ 56.67万 - 项目类别:
In Vivo Study of of Chemokine Antagonists for Cancer
癌症趋化因子拮抗剂的体内研究
- 批准号:
8829202 - 财政年份:2014
- 资助金额:
$ 56.67万 - 项目类别:
A NOVEL SMALL MOLECULE CX3CR1 ANTAGONIST HALTS METASTASIS
一种新型小分子 CX3CR1 拮抗剂可阻止转移
- 批准号:
9340341 - 财政年份:2014
- 资助金额:
$ 56.67万 - 项目类别:
Molecular Screening and Protein Expression Shared Resource
分子筛选和蛋白质表达共享资源
- 批准号:
10570944 - 财政年份:1997
- 资助金额:
$ 56.67万 - 项目类别:
Molecular Screening and Protein Expression Shared Resource
分子筛选和蛋白质表达共享资源
- 批准号:
10360641 - 财政年份:1997
- 资助金额:
$ 56.67万 - 项目类别:
Molecular Screening and Protein Expression Shared Resource
分子筛选和蛋白质表达共享资源
- 批准号:
9917711 - 财政年份:
- 资助金额:
$ 56.67万 - 项目类别:
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