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Mathematical Modeling of Biomolecule Translocation through Nanopores

通过纳米孔的生物分子易位的数学模型

基本信息

批准号：
8424268
负责人：
Hui Zhao
金额：
$ 6.93万
依托单位：
UNIVERSITY OF NEVADA LAS VEGAS
依托单位国家：
美国
项目类别：
财政年份：
2012
资助国家：
美国
起止时间：
2012-02-13 至 2015-07-31
项目状态：
已结题

项目摘要

DESCRIPTION (provided by applicant): The goal of this proposal seeks to develop a continuum-based mathematical model to gain a fundamental knowledge necessary to design a label-free, low-cost, high-speed, and high-throughput DNA sequencing method using nanopores. Nanopores are emerging as a promising candidate for the development of a third- generation sequencing device which will meet the goal of a $1,000 human genome sequencing paradigm set by the National Institute of Health. Many experimental data on DNA molecule translocation through a nanopore has been collected for the last decade, but a simple continuum-based model that describes the translocation process in statistical terms and can be directly compared with an ensemble average observed by experiments is still lacking. Limited existing analytical continuum models still cannot fully explain experimental observations. Simple physical arguments suggest that concentration polarization and the shape of the nanopore may be able to bridge the discrepancy of the tether force or translocation velocity between the experimental results and the theoretical predictions from existing simple continuum models. Thus the specific aims are to (1) Explore the role of concentration polarization using our proposed continuum-based mathematical model; (2) Examine the feasibility of using salt concentration imposed externally across the nanopore to regulate DNA translocation through numerical simulations; (3) Understand the effect of irregular shape of nanopores on DNA translocation. More accurate explicit relations between the translocation velocity and various conditions (e.g., salt concentration, nanopore dimension, surface charge, and the electric field intensity) will be determined by the proposed continuum model and ready to be directly compared with large amount of existing experimental data. Such information is important to understand the DNA translocation through a nanopore and further provides a knowledge base for rational design of experiments.

描述（由申请人提供）：本提案的目标是开发一种基于连续统的数学模型，以获得设计无标记、低成本、高速和高通量DNA测序方法所需的基础知识。纳米孔正在成为开发第三代测序装置的有希望的候选者，该第三代测序装置将满足美国国立卫生研究院设定的1,000美元人类基因组测序范例的目标。在过去的十年中，已经收集了许多关于DNA分子通过纳米孔易位的实验数据，但是仍然缺乏一个简单的基于连续统的模型，该模型以统计学术语描述了易位过程，并且可以直接与实验观察到的总体平均值进行比较。有限的现有分析连续统模型仍然不能完全解释实验观察。简单的物理参数表明，浓差极化和纳米孔的形状可能能够弥合实验结果与现有简单连续模型的理论预测之间的系绳力或易位速度的差异。因此，具体目标是（1）使用我们提出的基于连续介质的数学模型探索浓差极化的作用;（2）通过数值模拟检查使用外部施加在纳米孔上的盐浓度来调节DNA易位的可行性;（3）了解纳米孔的不规则形状对DNA易位的影响。易位速度和各种条件之间的更精确的显式关系（例如，盐浓度、纳米孔尺寸、表面电荷和电场强度）将由所提出的连续模型确定，并准备与大量现有的实验数据直接比较。这些信息对于理解DNA通过纳米孔的移位是重要的，并且进一步为实验的合理设计提供了知识基础。