Liquid Array Protein Assay Platform
Liquid Array Protein Assay Platform
批准号:
8045388
负责人:
DAVID M ROTHWARF
金额:
$63.12万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-03-01 至 2013-02-28
关键词:
AntibodiesAptamer TechnologyBasic ScienceBindingBinding ProteinsBiologicalBiological AssayChemistryClinicalCodeCommunicable DiseasesData AnalysesDetectionDevelopmentDiagnosisDiseaseEquipmentGenomicsHIVHealthHeart DiseasesHumanImageryIndustryKidney DiseasesLabelLiquid substanceLiver diseasesMagnetismMalignant NeoplasmsMethodsModelingMolecular ProfilingNucleic AcidsPerformancePhasePreparationProcessProtein Array AnalysisProtein BindingProteinsProteomeProteomicsProtocols documentationReagentReproducibilityRheumatoid ArthritisSamplingSerumShapesSignal TransductionSurfaceSystemTechniquesTechnologyTestingallergic responseaptamerbasecomputerized data processingcostcost effectivedesignflexibilityimprovedmanufacturing processmeetingsnoveloutcome forecastparticleprotein expressionprotein profilingprototyperesearch studysoftware developmenttool
中文摘要
该项目的目的是开发和优化我们的新型基于颗粒的微阵列平台ArrayableESP,
用于人血清样品的高度多重(50- 2000-plex)蛋白质组学分析。静电除尘器
光学编码的微加工粒子,可以使用磁力操纵。他们是
采用高效、稳健的技术,在市售的可再生能源设备上制造
从半导体行业借来的。它们在成本吞吐量、可扩展性
和灵活性。我们将使用适体,而不是抗体,
我们的平台,这将消除对样品预标记/预处理的需要,并允许并行
蛋白结合后的均相检测方法。结合ArrayableESP平台
与适体的结合有望提高分析的准确性并导致简化的工作流程。这些属性,
结合ArrayableESP平台提供的几乎无限的多路复用潜力,
多重产物具有显著优于目前可用的蛋白质组学分析技术的优点。ESP
技术具有广泛的适用性,应该是诊断,预后,
表征各种疾病状态,包括癌症、心脏病、关节炎和炎症
疾病、肾病、肝病、过敏反应和感染性疾病(例如HIV)。
英文摘要
The aim of this project is to develop and optimize our novel particle-based microarray platform, ArrayableESP,
for application to high multiplex (50- to 2000-plex) proteomic analysis of human serum samples. ESPs are
optically-encoded microfabricated particles that can be manipulated using magnetic force. They are
manufactured on commercially available photolithographic equipment using efficient and robust techniques
borrowed from the semi-conductor industry. They have significant advantages in cost throughput, scalability,
and flexibility over existing bead-based liquid array platforms. We will use aptamers, instead of antibodies, on
our platform, which will eliminate the need for sample pre-labeling/pre-processing and allow for a parallel
method of homogeneous detection following protein binding. The combination of the ArrayableESP platform
with aptamers is expected to increase accuracy of analysis and result in a simplified workflow. Such attributes,
in combination with the nearly unlimited multiplex potential offered by the ArrayableESP platform, will provide a
multiplex product with significant advantages over currently available technologies for proteomic analysis. ESP
technology has broad applicability and should be a valuable tool in the diagnosis, prognosis, and
characterization of a variety of disease states, including cancer, heart disease, arthritis and inflammatory
diseases, kidney disease, liver disease, allergic responses, and infectious diseases (e.g. HIV).
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批准号:7611293
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项目类别:
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资助金额:$10.0万
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财政年份:2009
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负责人:DAVID M ROTHWARF
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依托单位:
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项目类别:
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资助金额:$3.41万
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财政年份:1998
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依托单位:
MECHANISM OF REGULATION OF NV-KB
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项目类别:
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资助金额:$2.96万
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财政年份:1998
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负责人:DAVID M ROTHWARF
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依托单位:
MECHANISM OF REGULATION OF NV-KB
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项目类别:
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财政年份:1998
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依托单位:
海外基金