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Computational Design Engine for Accurate and Efficient Sequencing of DNA and RNA

Computational Design Engine for Accurate and Efficient Sequencing of DNA and RNA
用于准确、高效 DNA 和 RNA 测序的计算设计引擎
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

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中文摘要
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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.
期刊论文(68)
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会议论文
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.
33
    Modeling Macromolecular Transport through Channels
    Modeling macromolecular transport through protein and solid-state nanopores
    Modeling Macromolecular Transport for Sequencing Technologies
    Modeling macromolecular transport through protein and solid-state nanopores
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