Hybrid nanochannel arrays for single molecule linear, genome analysis
Hybrid nanochannel arrays for single molecule linear, genome analysis
批准号:
7291658
负责人:
Han Cao
金额:
$18.53万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-26 至 2009-03-16
关键词:
ArchitectureBiologicalBiological MarkersCaliberCellsCopy Number PolymorphismCytogeneticsDNADataDetectionDevelopmentDevicesEnvironmentExonsFutureGenesGeneticGenetic PolymorphismGenomeGenomic InstabilityGenomicsGoldHereditary DiseaseHybridsImageryIndividualIndustryIntronsLightMalignant NeoplasmsMarker DiscoveryMethodsMicrofluidicsMicroscopyNanomanufacturingNaturePatient CarePatternPharmacogenomicsPhasePlasticsPreparationPrincipal InvestigatorProcessProtocols documentationReaderRelative (related person)ResolutionSamplingSemiconductorsSignal TransductionSiliconSiteSolutionsStandards of Weights and MeasuresStatistically SignificantStructureTechnologyTransistorsbasebiochipcommercializationcostdesigndrug discoveryimprovedleukemiamalignant breast neoplasmnanochannelnanofluidicnanoimprint lithographynanoscaleprogramssingle moleculesizesubmicrontime useuser-friendly
中文摘要
描述(由申请人提供):本提案的长期目标是开发一种完全集成的芯片和阅读器,能够对线性化的原生状态基因组物质进行单分子分析。预期的实施例将允许直接可视化和分析直接从样品(可能是单个细胞)提取的DNA的百万碱基片段,分辨率优于400bp。此外,该芯片将适应以高通量方式对单个DNA分子进行大规模并行分析,从而及时提供统计相关数据。我们的方法将集中在纳米通道阵列的开发上,这是我们之前展示过的一种以大规模并行方式线性化DNA单分子的设备。该装置依赖于直径小于100纳米的通道阵列。当DNA流经这些通道时,它受到物理约束,被迫展开,从而允许使用荧光显微镜进行线性审讯。这样的分析可以大大提高我们对与癌症和其他遗传疾病有关的基因组不稳定性的理解。该器件商业化的关键考虑因素是纳米通道的设计和制造以及支持芯片架构。目前,该器件由硅组成,并使用纳米压印光刻(NIL)进行图案化。NIL是一种低成本、高通量的纳米制造工艺,是为半导体工业开发的一种进一步缩小传统集成电路中晶体管尺寸的手段。我们利用这项技术制造生物芯片。虽然这种方法非常适合于制造纳米级的特征,但还需要进一步发展,以适应直接从生物学家的移液管中提取的样品。我们假设理想的装置将需要一个从宏观溶液环境到纳米级通道的过渡区域。此外,我们预计,依靠传统的、基于塑料的微流体制造技术来实现微米级特征,以及基于硅的方法来实现亚微米级过渡,从而实现通道本身,这种转变是最经济的。这两种制造体制的整合至关重要。该项目的完成将产生一个单一的集成生物芯片设备,能够提供具有统计学意义的单分子分析,分辨率为400 bp。这种设备对单细胞、单分子分析的未来至关重要首席研究员/项目主任(最后、第一、中):Cao, Han Narrative长基因组DNA的单分子分析将通过提供有关遗传多态性本质的背景信息,使人们能够更好地理解和改进遗传疾病,特别是癌症的治疗。基于平行纳米通道的标准化平台可以作为未来患者护理中一致的高通量基因组分析的基础。
英文摘要
DESCRIPTION (provided by applicant): The long term objective of this proposal is to develop a fully integrated chip and reader capable of single molecule analysis of linearized, native state genomic material. The anticipated embodiment will permit direct visualization and analysis of megabase fragments of DNA extracted directly from a sample (possibly a single cell) with resolution better than 400 bp. Furthermore, the chip will accommodate massively parallel analyses of individual DNA molecules in a high-throughput manner thus providing statistically relevant data in a timely fashion. Our approach will focus on development of the nanochannel array, a device previously demonstrated by us to linearize single molecules of DNA in a massively parallel fashion. The device relies upon an array of channels with diameters less than 100 nm. As DNA is flowed through such channels, it becomes physically constrained and is forced to uncoil, thus permitting linear interrogation using fluorescent microscopy. Such analyses could serve to greatly enhance our understanding of genomic instabilities related to cancer and other genetic diseases. A critical consideration for the commercialization of this device is the design and manufacture of the nanochannels and supporting chip architecture. Currently the device is composed of silicon and patterned using nanoimprint lithography (NIL). NIL is a low cost, high throughput nanomanufacturing process developed for the semiconductor industry as a means of further reducing the size of transistors in traditional integrated circuits. We have leveraged this technology for the manufacture of bio chips. Though well-suited for creating nanoscale features, further development of the process is required to accommodate a sample derived directly from the biologist's pipette. We hypothesize that the ideal device will require a transitional region from a macroscopic solution environment to the nanoscale channels. Furthermore, we expect that this transition is most economically developed by relying on conventional, plastic-based microfluidic manufacturing technologies for micron-scale features and silicon based approaches for the sub-micron transition leading to the channels themselves. Integration of these two manufacturing regimes is of critical importance. Completion of this project will result in a single, integrated biochip device capable of providing statistically significant, single molecule analysis of megabase DNA with 400 bp resolution. Such a device will be crucial to the future of single cell, single molecule analyses Principal Investigator/Program Director (Last, First, Middle): Cao, Han Narrative Single molecule analysis of long, genomic DNA will enable greater understanding and improved treatment of genetic diseases, especially cancer, by providing contextual information as to the nature of genetic polymorphisms. A standardized platform based on parallel nanochannels could serve as a basis for consistent, high-throughput genomic analyses in future patient care.
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会议论文
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资助金额:$10.0万
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批准号:7224766
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资助金额:$13.2万
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项目类别:
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资助金额:$13.2万
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负责人:Han Cao
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依托单位:
海外基金