Highly sensitive proteomics method to probe cell heterogeneity at single cell resolution
Highly sensitive proteomics method to probe cell heterogeneity at single cell resolution
批准号:
10693198
负责人:
Yu Gao
金额:
$39.41万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-01 至 2024-06-30
关键词:
BacteriaCell LineCellsCellular StructuresChemicalsClassificationCoupledCreativenessDataDetectionDevelopmentDiagnosisDiseaseEventEvolutionFosteringGoalsHealthHeterogeneityIndividualInvestmentsKnowledgeLabelMammalian CellMeasuresMessenger RNAMethodsMissionMitochondriaNational Institute of General Medical SciencesNeoplasm MetastasisNeurodegenerative DisordersPeptidesPharmaceutical PreparationsPharmacotherapyPhosphorylationPost-Translational Protein ProcessingPreventionProteomeProteomicsPublic HealthResearchResearch PersonnelResearch SupportResolutionResourcesScientific Advances and AccomplishmentsSignal TransductionStatistical ModelsStrategic PlanningUnited States National Institutes of Healthdevelopmental neurobiologydriving forcehuman diseaseimprovedinformatics toolinnovationinsightionizationneuron developmentneuronal tumornew technologynovelprotein expressiontranscriptomicstumor
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary/Abstract:
As the single-cell transcriptomics analysis becomes more accessible, individual cells
can now be classified individually, allowing us to understand cell heterogeneity as one of the
key driving forces in neuron development and tumor evolution. However, the presence of
mRNA is not always coupled with protein expression, single-cell proteomics will provide a more
precise view of the cell components and signaling, including key post-translational modification
events such as phosphorylation.
Here we propose to combine several different strategies to develop a highly sensitive
proteomics method to probe cell heterogeneity at single cell resolution. Specifically, we will 1)
develop chemical labeling probes to enhance peptide ionization; 2) develop an isobaric
isotopologue labeling approach to quantify single mammalian cell from various cell lines; 3)
develop informatics tools and statistical models to resolve cell heterogeneity at single-cell
resolution with non-single-cell proteomics data. Each of these proposed methods alone, could
potentially enable us to measure the proteome of a single mammalian cell. When combined,
they will result in a highly sensitive platform that could potentially allow us to probe the
proteome at the level of a single mitochondria or bacteria.
The long-term goal of this project is to elucidate the fundamental mechanisms of the
origin and implications of cell heterogeneity. This proposed research is highly relevant to public
health in the fields of tumor evolution, cancer metastasis, developmental neurobiology and
neurodegenerative disease. Understanding cell heterogeneity will help us to develop more
effective drug treatments to many diseases. Therefore, the proposed research is relevant to
the part of NIH's mission that fosters “fundamental creative discoveries, innovative research
strategies, and their applications as a basis for ultimately protecting and improving health” and
that “supports research in the causes, diagnosis, prevention, and cure of human diseases.”
The proposed research is relevant to the NIGMS 2015-2020 strategic plan: “Objective 1-1:
Invest in and sustain a broad and diverse portfolio of highly meritorious research.”, “Objective
1-2: Promote the ability of investigators to pursue new research directions, novel scientific
insights and innovative ideas”, and “Objective 3-1: Support access to essential research
resources and the development of new technologies that enable novel scientific advances.”
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1021/acs.jproteome.2c00358
发表时间:
2023-02-03
期刊:
JOURNAL OF PROTEOME RESEARCH
影响因子:
4.4
作者:
[Shao, Xinhao, Grams, Christopher, Gao, Yu]
通讯作者:
Gao, Yu
DOI:
10.1021/acs.jproteome.2c00477
发表时间:
2023-01-06
期刊:
JOURNAL OF PROTEOME RESEARCH
影响因子:
4.4
作者:
[Zhang, Ziwei, Gao, Yu]
通讯作者:
Gao, Yu
DOI:
10.1093/nar/gkac1009
发表时间:
2023-01-06
期刊:
NUCLEIC ACIDS RESEARCH
影响因子:
14.9
作者:
[Shao, Xinhao, Gomez, Clarissa D., Kapoor, Nandini, Considine, James M., Grams, Christopher, Gao, Yu (Tom), Naba, Alexandra]
通讯作者:
Naba, Alexandra
Enhanced mass-spectrometry-based approaches for in-depth profiling of the cancer extracellular matrix
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批准号:10493806
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项目类别:
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资助金额:$21.11万
-
财政年份:2022
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负责人:Yu Gao
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依托单位:
Thinking outside the cell: Leveraging HuBMAP data to build the human ECM atlas
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批准号:10816692
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项目类别:
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资助金额:$15.0万
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财政年份:2022
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负责人:Yu Gao
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依托单位:
Thinking outside the cell: Leveraging HuBMAP data to build the human ECM atlas
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批准号:10649523
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项目类别:
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资助金额:$46.5万
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财政年份:2022
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负责人:Yu Gao
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依托单位:
Thinking outside the cell: Leveraging HuBMAP data to build the human ECM atlas
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批准号:10527519
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项目类别:
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资助金额:$46.5万
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财政年份:2022
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负责人:Yu Gao
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依托单位:
Enhanced mass-spectrometry-based approaches for in-depth profiling of the cancer extracellular matrix
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批准号:10704135
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项目类别:
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资助金额:$20.66万
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财政年份:2022
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负责人:Yu Gao
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依托单位:
Highly sensitive proteomics method to probe cell heterogeneity at single cell resolution
-
批准号:10225325
-
项目类别:
-
资助金额:$39.41万
-
财政年份:2019
-
负责人:Yu Gao
-
依托单位:
Highly sensitive proteomics method to probe cell heterogeneity at single cell resolution
-
批准号:9796389
-
项目类别:
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资助金额:$39.41万
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财政年份:2019
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负责人:Yu Gao
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依托单位:
Highly sensitive proteomics method to probe cell heterogeneity at single cell resolution
-
批准号:10449281
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项目类别:
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资助金额:$39.41万
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财政年份:2019
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负责人:Yu Gao
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依托单位:
Highly sensitive proteomics method to probe cell heterogeneity at single cell resolution
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批准号:10001554
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项目类别:
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资助金额:$39.41万
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财政年份:2019
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负责人:Yu Gao
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依托单位:
Neurobiological characteristics, parent-child relationships, and conduct problems in adolescence: A longitudinal multimodal neuroimaging study
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批准号:9924570
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项目类别:
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资助金额:$39.25万
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财政年份:2018
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负责人:Yu Gao
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依托单位:
A brain imaging study on conditioning deficits in antisocial youths
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批准号:9281086
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项目类别:
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财政年份:2016
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负责人:Yu Gao
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依托单位:
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批准号:8712529
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项目类别:
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资助金额:$15.26万
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财政年份:2012
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负责人:Yu Gao
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依托单位:
Biomarkers for conduct problems: Abnormal conditioning to punishments and rewards
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批准号:8339175
-
项目类别:
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资助金额:$15.7万
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财政年份:2012
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负责人:Yu Gao
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依托单位:
Biomarkers for conduct problems: Abnormal conditioning to punishments and rewards
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批准号:8541043
-
项目类别:
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资助金额:$14.9万
-
财政年份:2012
-
负责人:Yu Gao
-
依托单位:
海外基金