Computational Design Engine for Accurate and Efficient Sequencing of DNA and RNA
Computational Design Engine for Accurate and Efficient Sequencing of DNA and RNA
批准号:
10621544
负责人:
MURUGAPPAN MUTHUKUMAR
金额:
$15.51万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-06-06 至 2023-05-31
关键词:
AddressAdoptionAlgorithmsChromosomesDNADNA sequencingDetectionElectrostaticsElementsEntropyEnzymesExperimental DesignsGenomeGoalsLawsLengthLocationMethodsMissionModificationNational Human Genome Research InstituteNoiseNucleic acid sequencingOutputPhysicsPolymersPositioning AttributeProteinsProtocols documentationRNAResearchSignal TransductionSodium ChlorideStructureTechniquesTechnologyTemperatureThermodynamicsTimeTranscriptViscosityalgorithm developmentaqueousbasecostdesignelectric fieldinnovationmulti-scale modelingnanofluidicnanoporenovelpressuresoundsuccesstechnology developmenttheoriestranscriptome sequencingvoltage
中文摘要
项目总结
英文摘要
PROJECT SUMMARY
The need to develop low-cost, rapid, and high-quality technologies for sequencing mammalian-
sized genomes has inspired many nanopore-based methods. All of these methods suffer from two
huge bottlenecks, which prohibit the required precision, and hence hinder the adoption of any of
these methods as a practical technology as of today. These bottlenecks are: (1) undesirable noise
levels for positioning DNA bases at read-out positions, and (2) difficulty in controlling capture
of large DNA molecules at the nanopore. By tackling these two critical challenges, we propose
to build a Computational Design Engine (CDE) to enable sequencing of DNA and RNA at the
maximum accuracy allowed by laws of physics.
The first aim is to reduce the positional noise of bases as DNA is being read. This goal will
be accomplished by innovative implementation of ideas based on stochastic resonance, ratchet
rectification, protein-assisted noise reduction, and non-enzymatic electrostatic traps. The proposed CDE will be able to design optimum features of AC fields, on top of ratcheting forces from enzymes and voltage gradients.
The second aim is to enhance capture of very large DNA and RNA molecules at the nanopore
for subsequent sequencing. The construction of the engine will incorporate all critical components
contributing to capture: entropic barriers, internal structures of RNA, entanglement effects of
DNA, electrostatics, electrohydrodynamics, and nanofluidics. The engine will design the best
experimental protocols, by optimum combinations of various contributing forces, to regulate the
capture efficiency of very large DNA and RNA.
For both aims, a broad suite of multi-scale modeling, and advanced theories of polymer physics
and non-equilibrium thermodynamics, will be used in innovative ways. The proposed CDE will put
theoretical bounds, based on sound laws of polymer physics, on sequencing accuracy in various
methods being pursued and how to attain their maximum capacities, and to designing better
alternative technologies.
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Translocation of an Incompressible Vesicle through a Pore.
不可压缩的囊泡通过孔隙的转移。
DOI:
10.1021/acs.jpcb.6b02079
发表时间:
2016-07-07
期刊:
The journal of physical chemistry. B
影响因子:
--
作者:
[Shojaei HR, Muthukumar M]
通讯作者:
Muthukumar M
DOI:
10.1021/nn3051677
发表时间:
2013-02-26
期刊:
ACS NANO
影响因子:
17.1
作者:
[Anderson, Brett N., Muthukumar, Murugappan, Meller, Amit]
通讯作者:
Meller, Amit
DOI:
10.1021/ma801799e
发表时间:
2009-02-24
期刊:
MACROMOLECULES
影响因子:
5.5
作者:
[Kumar, Rajeev, Kundagrami, Arindam, Muthukumar, M.]
通讯作者:
Muthukumar, M.
Boundaries of the Topologically Frustrated Dynamical State in Polymer Dynamics
聚合物动力学中拓扑受阻动力学状态的边界
DOI:
10.1021/acsmacrolett.2c00019
发表时间:
2022
期刊:
ACS Macro Letters
影响因子:
7.015
作者:
[Chen, Kuo, Li, Siao-Fong, Muthukumar, M.]
通讯作者:
Muthukumar, M.
Langevin dynamics simulation of DNA ejection from a phage.
噬菌体 DNA 喷射的 Langevin 动力学模拟。
DOI:
10.1007/s10867-013-9316-x
发表时间:
2013
期刊:
Journal of biological physics
影响因子:
1.8
作者:
[Mahalik,JP, Hildebrandt,B, Muthukumar,M]
通讯作者:
Muthukumar,M
共 33 条
Modeling Macromolecular Transport through Channels
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批准号:6753503
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项目类别:
-
资助金额:$26.83万
-
财政年份:2003
-
负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling macromolecular transport through protein and solid-state nanopores
-
批准号:8572936
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项目类别:
-
资助金额:$26.87万
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财政年份:2003
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负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling Macromolecular Transport for Sequencing Technologies
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批准号:8134463
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项目类别:
-
资助金额:$26.53万
-
财政年份:2003
-
负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling macromolecular transport through protein and solid-state nanopores
-
批准号:8728977
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项目类别:
-
资助金额:$26.29万
-
财政年份:2003
-
负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Computational Design Engine for Accurate and Efficient Sequencing of DNA and RNA
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批准号:10190987
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项目类别:
-
资助金额:$34.73万
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财政年份:2003
-
负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling Macromolecular Transport through Channels
-
批准号:6599363
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项目类别:
-
资助金额:$31.83万
-
财政年份:2003
-
负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling Macromolecular Transport for Sequencing Technologies
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批准号:8289501
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项目类别:
-
资助金额:$26.56万
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财政年份:2003
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负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling Macromolecular Transport through Protein Channels and Nanopores
-
批准号:7264179
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项目类别:
-
资助金额:$26.59万
-
财政年份:2003
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负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling Macromolecular Transport through Protein Channels and Nanopores
-
批准号:7619016
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项目类别:
-
资助金额:$26.08万
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财政年份:2003
-
负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling Macromolecular Transport for Sequencing Technologies
-
批准号:7978448
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项目类别:
-
资助金额:$26.76万
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财政年份:2003
-
负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling Macromolecular Transport through Channels
-
批准号:6897443
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项目类别:
-
资助金额:$26.83万
-
财政年份:2003
-
负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
Modeling Macromolecular Transport through Protein Channels and Nanopores
-
批准号:7418952
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项目类别:
-
资助金额:$26.08万
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财政年份:2003
-
负责人:MURUGAPPAN MUTHUKUMAR
-
依托单位:
海外基金