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Application of Polymer Reaction Modeling to Nonenzymatic Polynucleotide Replication

机译:聚合物反应模型在非酶多核苷酸复制中的应用

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Methods of polymer reaction engineering were used to develop a mechanistic model of nonenzymatic polynucleotide replication. The model is made possible by the rate constants developed by Rajamani et al. This model treats the ideas of stalling proposed by Rajamani in a direct kinetic mechanism. When one assumes that multiple incorrect insertions in a row are unlikely, the model returns estimates of the error threshold very much in agreement with the modified Eigen model (based on probability arguments) proposed by Rajamani. In addition, the current model gives average lengths of polynucleotides, categorized by ultimate nucleoside (type and correct/incorrect) as well as the average lengths of interior and terminal sequences of correct and incorrect insertions in a row. When the insights of Leu et al. (specifically, that incorrect additions following an incorrect addition are likely) are included into the model, the error threshold will drop to unrealistic levels. To compensate for this, a mechanism for the "recycle" of incorrect strands (via hydrolysis and repolymerization) was included. Calculations indicate that even with a "correction" mechanism (hydrolysis of chain containing errors), the error threshold drops to an unacceptable value.
机译:聚合物反应工程方法被用于建立非酶多核苷酸复制的机理模型。 Rajamani等人开发的速率常数使该模型成为可能。该模型在直接动力学机制中处理了Rajamani提出的失速想法。当假设不可能连续出现多个错误插入时,该模型将返回错误阈值的估计值,这与Rajamani提出的修改后的Eigen模型(基于概率论证)非常一致。另外,当前模型给出了按最终核苷(类型和正确/不正确)分类的多核苷酸的平均长度,以及连续正确和错误插入的内部和末端序列的平均长度。当Leu等人的见解。 (特别是在错误添加之后,可能会添加错误),该错误阈值将降至不切实际的水平。为了弥补这一点,包括了一种“循环”错误链(通过水解和再聚合)的机制。计算表明,即使采用“校正”机制(包含错误的链水解),错误阈值也会下降到不可接受的值。

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