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Computational Principles of Primer Design for Site Directed Mutagenesis

机译:定点诱变引物设计的计算原理

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摘要

Site directed mutagenesis (SDM) is a method to alter DNA molecules with intentionally designed mutations. SDM creates mutated copies of the original sequence as follows: an oligonucleotide primer hybridizes to the DNA template to form a duplex with base mismatches or single-stranded DNA loops. Then, DNA polymerase extends the primer to create a mutated copy of the initial DNA molecule. In this work, we address the problem of designing optimal primers to introduce single or multiple site mutations, deletions, or insertions. Our approach is based on three principles. First, for mutations that introduce amino-acid substitutions, preference in codon replacement is given to changes that minimize the number of nucleotide substitutions. Second, codons vary in the frequency with which they are incorporated into successful mutants, so highly successful codons are favored. We conducted a series of SDM experiments to determine success rates for all codons. These rates are used in primer design. Third, primer length and primer position relative to the mutated site is chosen to minimize duplex free energy, and thus maximize duplex stability.
机译:定点诱变(SDM)是一种通过故意设计的突变来改变DNA分子的方法。 SDM如下创建原始序列的突变拷贝:寡核苷酸引物与DNA模板杂交,形成具有碱基错配或单链DNA环的双链体。然后,DNA聚合酶延伸引物以产生初始DNA分子的突变拷贝。在这项工作中,我们解决了设计最佳引物以引入单或多个位点突变,缺失或插入的问题。我们的方法基于三个原则。首先,对于引入氨基酸替代的突变,密码子替代优先考虑最小化核苷酸替代数目的改变。其次,密码子掺入成功突变体的频率不同,因此,高度成功的密码子受到青睐。我们进行了一系列SDM实验,以确定所有密码子的成功率。这些比率用于引物设计。第三,选择引物长度和相对于突变位点的引物位置以最小化双链体自由能,从而最大化双链体稳定性。

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