Development of new tools for Single Cell Analysis

开发单细胞分析新工具

• 批准号: 8197062
• 负责人: DAVID R. WALT
• 金额: $ 33.89万
• 依托单位: TUFTS UNIVERSITY MEDFORD
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-11-18 至 2013-10-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8197062
• 关键词: Address; Age; Age Factors; Aging; Alleles; Area; Bacterial Antibiotic Resistance; Bacterial Infections; Behavior; Biochemistry; Biological Assay; Biology; Biomedical Engineering; Cells; Cellular biology; Chemistry; Chromosome Mapping; Clinical; Complex; Cytolysis; DNA; Data Set; Detection; Development; Diagnostic; Disease; Enzymes; Escherichia coli; Exhibits; Fiber Optics; Frequencies; Genetic; Genetic Crosses; Genetic Population Study; Genetic Recombination; Genetic Variation; Genome; Genomics; Genotype; Goals; Heterogeneity; Individual; Investigational Therapies; Lead; Malignant Neoplasms; Maps; Masks; Measurement; Messenger RNA; Methods; Modeling; Molecular Biology; Molecular Structure; Monitor; Neoplasm Metastasis; Normal Cell; Outcome; Phenotype; Population; Population Genetics; Principal Investigator; Proteins; Regimen; Regulator Genes; Relative (related person); Research Personnel; Resolution; SNP genotyping; Sampling; Somatic Mutation; Surface; System; Technology; Therapeutic; Tissues; Variant; base; biological research; cell type; cost; graduate student; human male; improved; interest; neoplastic cell; new technology; novel; public health relevance; response; single cell analysis; single molecule; sperm cell; statistics; success; tool; tumor progression

DESCRIPTION (provided by applicant): Single cell analysis is becoming increasingly important as it is clear that ensemble measurements mask the diversity of the biology in cell populations. Single cell genotyping and phenotyping are necessary to define functional heterogeneity in varying cell types including diseased vs. normal cells. The overall goal of this project is to develop new bioanalytical tools for performing high resolution single cell analysis. This interdisciplinary project involves Chemistry, Molecular Biology, Biochemistry, Genetics, and Bioengineering and will be conducted by a team including a senior Principal Investigator, one postdoctoral associate, and two graduate students. Specific Aim 1-Develop a high fidelity single DNA molecule genotyping approach for analyzing thousands of molecules simultaneously and with the ability to interrogate multiple SNPs. We plan to employ fiber optic microwell arrays to develop a robust, efficient, fast, and affordable method of simultaneously genotyping single DNA molecules from thousands of individual cells. Specific Aim 2-Develop an approach to isolating single cells, capturing genomic DNA, and genotyping the captured DNA. In this Aim, we will apply the methods developed in Specific Aim 1 to whole cells. Thousands of single E. coli cells will be captured in individual wells, lysed, genomic DNA fragmented, the DNA captured on the surface of the individual wells, and then genotyped. Specific Aim 3-Develop a high resolution single molecule analysis method for analyzing the contents of single cells. We will develop methods for performing high resolution single molecule counting of the contents of individual cells. Single cells will be isolated, lysed, and their contents will be captured in microwell arrays such that individual mRNA and protein molecules are isolated. We will then use a variety of methods that enable us to count the individual molecules. Success of these aims will provide a powerful new technology broadly applicable to multiple areas of biological research. For biologists, it provides the ability to describe the complex genetics of cell populations, providing clinicians with improved opportunities for diagnostics, and relating population genetics with responses to therapy and clinical outcomes. For experimentalists, it provides new ways to study phenomena such as tumor progression and responses to experimental therapies. For researchers on aging, it provides the ability to monitor changes in somatic genetics with age and the factors influencing them. For geneticists, it provides a low cost ability to construct genetic maps, to identify trans-acting elements controlling recombination, and to monitor the molecular structure of recombination products with high resolution. Our long term goal is to apply the developed technology to a variety of cell types to study fundamental cell biology and to understand how cell-to-cell and cell population differences may lead to different cell fates and may define disease. PUBLIC HEALTH RELEVANCE: Individual cells in a population, such as are present in bacterial infections, as well as diseased tissues such as cancer, exhibit random behaviors such that different cells may behave quite differently relative to the average behavior of the population and can lead to such conditions as bacterial antibiotic resistance and cancer metastasis. The goal of this project is to develop new tools for analyzing single cells to characterize and understand the differences between cells in a population.

描述（由申请人提供）：单细胞分析变得越来越重要，因为很明显，整体测量掩盖了细胞群体中生物学的多样性。单细胞基因分型和表型分析对于定义不同细胞类型（包括患病细胞与正常细胞）的功能异质性是必要的。该项目的总体目标是开发新的生物分析工具来进行高分辨率单细胞分析。这个跨学科项目涉及化学、分子生物学、生物化学、遗传学和生物工程，将由包括一名高级首席研究员、一名博士后助理和两名研究生在内的团队进行。具体目标 1 - 开发一种高保真度单 DNA 分子基因分型方法，用于同时分析数千个分子，并具有询问多个 SNP 的能力。我们计划利用光纤微孔阵列开发一种稳健、高效、快速且经济实惠的方法，同时对数千个单个细胞中的单个 DNA 分子进行基因分型。具体目标 2 - 开发一种分离单细胞、捕获基因组 DNA 并对捕获的 DNA 进行基因分型的方法。在此目标中，我们将在特定目标 1 中开发的方法应用于整个细胞。将在各个孔中捕获数千个单个大肠杆菌细胞，将其裂解，将基因组 DNA 片段化，将 DNA 捕获在各个孔的表面上，然后进行基因分型。具体目标3-开发用于分析单细胞内容物的高分辨率单分子分析方法。我们将开发对单个细胞的内容物进行高分辨率单分子计数的方法。单细胞将被分离、裂解，其内容物将被捕获在微孔阵列中，从而分离出单个 mRNA 和蛋白质分子。然后我们将使用各种方法来计算单个分子的数量。这些目标的成功将提供一种广泛适用于生物研究多个领域的强大新技术。对于生物学家来说，它提供了描述细胞群复杂遗传学的能力，为临床医生提供了更好的诊断机会，并将群体遗传学与治疗反应和临床结果联系起来。对于实验学家来说，它提供了研究肿瘤进展和对实验疗法的反应等现象的新方法。对于衰老研究人员来说，它提供了监测体细胞遗传学随年龄变化及其影响因素的能力。对于遗传学家来说，它提供了构建遗传图谱、识别控制重组的反式作用元件以及以高分辨率监测重组产物的分子结构的低成本能力。我们的长期目标是将开发的技术应用于各种细胞类型，以研究基础细胞生物学，并了解细胞间和细胞群的差异如何导致不同的细胞命运并定义疾病。 公共卫生相关性：群体中的单个细胞（例如细菌感染中存在的细胞）以及患病组织（例如癌症）表现出随机行为，因此不同细胞的行为可能与群体的平均行为截然不同，并可能导致细菌抗生素耐药性和癌症转移等情况。该项目的目标是开发用于分析单细胞的新工具，以表征和理解群体中细胞之间的差异。