A Spatially coarse-grained, rule-based frame work for modeling large molecular
A Spatially coarse-grained, rule-based frame work for modeling large molecular
批准号:
8892207
负责人:
Jeremy S Edwards
金额:
$31.19万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-07-05 至 2018-04-30
关键词:
AddressAntigensCell membraneCellsCerealsComplexCytosolDataDevelopmentEpidermal Growth Factor ReceptorExplosionFc epsilon RIIgEMethodologyMicroscopicModelingMolecularNatureRelative (related person)Signal TransductionSystemVascular Endothelial Growth Factor ReceptorWorkbasecombinatorialcrosslinkexperiencenetwork modelsreceptorsimulationspatial neglecttool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The development of mathematical tools to simulate signaling dynamics is extremely important. Based on our previous experimental data and simulation results, we are convinced that to accurately and appropriately model signaling networks, we cannot neglect the spatial organization of the cell membrane (and ultimately the cytosol as well). We have extensive experience in developing spatially realistic simulations of the cell membrane and studied the initiation of signaling. However, while these simulations are extremely computationally intense, crucial aspects of cell signaling can only be correctly represented in the context of the entire cell membrane, or at least a significant portion of it. Th Fc¿RI system presents an additional challenge relative to other commonly studied receptor systems (i.e. EGFR, VEGFR), in that the Fc¿RI/IgE complex essentially behaves as a bivalent receptor, while the antigens are typically multivalent (valency from 3 to ¿24). As a result, arbitrarily large aggregates may emerge through the multivalent cross-linking of FceRI/IgE complexes by the antigen. Due to the combinatorial explosion of the number of possible aggregate types, this problem is eminently suited for the rule-based approach to bio-molecular network modeling. Thus, the nature of the FceRI/IgE system requires the integration of the rule-based approach with a spatial modeling framework. We will develop a coarse grained methodology for integration of detailed (microscopic) and cell-level (mesoscopic) simulations and experimental results. This framework will help address both challenges described above, namely (a) integrate detailed, microscopic simulations and experimental data into a mesoscopic model that captures a significant portion of the cell membrane and (b) provide a mechanism to include spatial mobility and steric constraints for large molecular aggregates in a rule-based, stochastic model of the Fc epsilon RI system.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
Analytical solution of steady-state equations for chemical reaction networks with bilinear rate laws.
具有双线性速率定律的化学反应网络稳态方程的解析解。
DOI:
10.1109/tcbb.2013.41
发表时间:
2013
期刊:
IEEE/ACM transactions on computational biology and bioinformatics
影响因子:
--
作者:
[Halász,AdámM, Lai,Hong-Jian, McCabePryor,Meghan, Radhakrishnan,Krishnan, Edwards,JeremyS]
通讯作者:
Edwards,JeremyS
Knowledge Management Center for Illuminating the Druggable Genome
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批准号:10598542
-
项目类别:
-
资助金额:$94.01万
-
财政年份:2018
-
负责人:Jeremy S Edwards
-
依托单位:
Haplotype Resolved Sequencing Technology
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批准号:8728983
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项目类别:
-
资助金额:$44.1万
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财政年份:2013
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负责人:Jeremy S Edwards
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依托单位:
Haplotype Resolved Sequencing Technology
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批准号:8568163
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项目类别:
-
资助金额:$45.0万
-
财政年份:2013
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负责人:Jeremy S Edwards
-
依托单位:
A Spatially coarse-grained, rule-based frame work for modeling large molecular
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批准号:8446651
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项目类别:
-
资助金额:$33.79万
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财政年份:2012
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负责人:Jeremy S Edwards
-
依托单位:
A Spatially coarse-grained, rule-based frame work for modeling large molecular
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批准号:8503615
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项目类别:
-
资助金额:$32.54万
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财政年份:2012
-
负责人:Jeremy S Edwards
-
依托单位:
A Spatially coarse-grained, rule-based frame work for modeling large molecular
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批准号:8656139
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项目类别:
-
资助金额:$33.46万
-
财政年份:2012
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负责人:Jeremy S Edwards
-
依托单位:
Polony Sequencing and the $1000 Genome
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批准号:7976897
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项目类别:
-
资助金额:$104.78万
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财政年份:2010
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负责人:Jeremy S Edwards
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依托单位:
Polony Sequencing and the $1000 Genome
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批准号:8324730
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项目类别:
-
资助金额:$84.32万
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财政年份:2010
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负责人:Jeremy S Edwards
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依托单位:
Polony Sequencing and the $1000 Genome
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批准号:8134450
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项目类别:
-
资助金额:$83.92万
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财政年份:2010
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负责人:Jeremy S Edwards
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依托单位:
UNM MODELING
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批准号:7905561
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项目类别:
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资助金额:$16.35万
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财政年份:2009
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负责人:Jeremy S Edwards
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依托单位:
Modeling and Bioinformatics Core
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批准号:8919395
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项目类别:
-
资助金额:$44.34万
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财政年份:2009
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负责人:Jeremy S Edwards
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依托单位:
Modeling and Bioinformatics Core
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批准号:8873025
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项目类别:
-
资助金额:$52.54万
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财政年份:2009
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负责人:Jeremy S Edwards
-
依托单位:
Sequencing Chr. 6 in Melanoma Patients
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批准号:7501225
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项目类别:
-
资助金额:$20.25万
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财政年份:2008
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负责人:Jeremy S Edwards
-
依托单位:
Sequencing Chr. 6 in Melanoma Patients
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批准号:7683895
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项目类别:
-
资助金额:$16.88万
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财政年份:2008
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负责人:Jeremy S Edwards
-
依托单位:
Polony Sequencing the Human Genome
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批准号:7477273
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项目类别:
-
资助金额:$30.0万
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财政年份:2007
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负责人:Jeremy S Edwards
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依托单位:
Polony Sequencing the Human Genome
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批准号:7320995
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项目类别:
-
资助金额:$30.0万
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财政年份:2007
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负责人:Jeremy S Edwards
-
依托单位:
Polony Sequencing the Human Genome
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批准号:7665566
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项目类别:
-
资助金额:$30.0万
-
财政年份:2007
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负责人:Jeremy S Edwards
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依托单位:
COBRE:UDE CHEM ENG: ASSAYS & MODELING PROTEIN SEQUENCE
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批准号:7170349
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项目类别:
-
资助金额:$15.81万
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财政年份:2005
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负责人:Jeremy S Edwards
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依托单位:
COBRE:UDE CHEM ENG: ASSAYS & MODELING TO ID PROTEIN
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批准号:7011794
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项目类别:
-
资助金额:$19.16万
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财政年份:2004
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负责人:Jeremy S Edwards
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依托单位:
UNM MODELING
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批准号:8309118
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项目类别:
-
资助金额:$15.07万
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财政年份:--
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负责人:Jeremy S Edwards
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依托单位:
国内基金
海外基金
Neo-antigens暴露对肾移植术后体液性排斥反应的影响及其机制研究
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批准号:2022J011295
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项目类别:省市级项目
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资助金额:10.0万元
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批准年份:2022
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负责人:王亚伟
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依托单位:
结核分枝杆菌持续感染期抗原(latency antigens)的重组BCG疫苗研究
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批准号:30801055
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项目类别:青年科学基金项目
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资助金额:19.0万元
-
批准年份:2008
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负责人:王丽梅
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依托单位: