Computer Program for Primer Design for Loop-Mediated Isothermal Amplification (LAMP)

L. U. Akhmetzianova
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Abstract

Introduction. To date, numerous methods of nucleic acid amplification have been proposed, and each method has a number of advantages and disadvantages. One of the most popular methods is Loop-mediated isothermal AMPlification (LAMP). Unlike thermocyclic reactions, such as PCR (polymerase chain reaction), which require three temperature changes and expensive equipment, in LAMP, the entire reaction takes place at one and the same temperature and at the maximum rate possible. An important component of LAMP-amplification is primers (usually 20–25 nucleotides), which need to be matched to a specific part of the nucleotide sequence. It is known that DNA sequence contains four nucleotides: A — adenine and T — thymine, G — guanine and C — cytosine. There is a huge variety of permutations of these nucleotides, and it is practically impossible to analyze such a large amount of data manually. Therefore, there is a need to use modern computer technologies. More than 150 computer programs have been proposed for the design of PCR primers, while for LAMP-primers there are less than 10 of them, and each of them has a number of drawbacks, e.g., in terms of the length of the analyzed site. Therefore, this work is aimed at developing a new domestic computer program for the design of specific primers for LAMP.Materials and Methods. The primer search algorithm was based on a linear search for a substring in a string, taking into account the criteria of primer selection for LAMP. The program complex of LAMP-primer design was implemented in Python programming language. The bioPython library was used to work with various DNA and RNA, and the Qt framework was used to develop the interface.Results. A modification of the direct sampling method using a stencil approach was proposed, taking into account the GC composition and annealing temperature of primers depending on their structure. A software package with a friendly interface was developed. It took into account the design criteria of primers: certificates of registration of computer programs (LAMPrimers iQ No. 2022617417 dated April 20, 2022, LAMPrimers iQ_loop No. 2023662840 dated June 14, 2023) were received. The program is in the public domain at https://github.com/Restily/LAMPrimers-iQDiscussion and Conclusion. The developed software packages can be used for research and analysis in molecular biology and genetics, to create diagnostic test systems that provide high sensitivity and reliability of detection of specific DNA and RNA. The software packages can be used in research institutes and laboratories engaged in the amplification of nucleic acids. The results of evaluating the selected sets of primers for the LAMP reaction were tested, and the effectiveness of working sets using the LAMPrimers iQ program was experimentally proven by the example of the detection of genetic material of the SARS-CoV-2 coronavirus.
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环路介导等温扩增(LAMP)引物设计计算机程序
导言。迄今为止,已提出了许多核酸扩增方法,每种方法都有一些优缺点。最流行的方法之一是环路介导等温扩增(LAMP)。与 PCR(聚合酶链反应)等需要三次温度变化和昂贵设备的热循环反应不同,在 LAMP 中,整个反应在一个相同的温度下以尽可能高的速率进行。LAMP 扩增的一个重要组成部分是引物(通常为 20-25 个核苷酸),需要与核苷酸序列的特定部分相匹配。众所周知,DNA 序列包含四个核苷酸:A - 腺嘌呤和 T - 胸腺嘧啶,G - 鸟嘌呤和 C - 胞嘧啶。这些核苷酸的排列组合种类繁多,要人工分析如此大量的数据实际上是不可能的。因此,有必要使用现代计算机技术。目前,用于设计 PCR 引物的计算机程序已超过 150 种,而用于设计 LAMP 引物的计算机程序还不到 10 种,而且每种程序都有许多缺点,例如在分析位点的长度方面。因此,这项工作旨在开发一种新的国产计算机程序,用于设计 LAMP 的特定引物。引物搜索算法基于对字符串中子串的线性搜索,同时考虑到 LAMP 引物选择的标准。LAMP 引物设计的程序综合体是用 Python 编程语言实现的。bioPython 库用于处理各种 DNA 和 RNA,Qt 框架用于开发界面。考虑到引物的 GC 组成和退火温度取决于引物的结构,提出了使用模板方法对直接取样法进行修改的建议。开发了一个界面友好的软件包。它考虑到了引物的设计标准:计算机程序注册证书(2022 年 4 月 20 日 LAMPrimers iQ 编号 2022617417,2023 年 6 月 14 日 LAMPrimers iQ_loop 编号 2023662840)已收到。该程序在 https://github.com/Restily/LAMPrimers-iQDiscussion 和 Conclusion 网站上属于公共领域。开发的软件包可用于分子生物学和遗传学的研究和分析,以创建诊断测试系统,提供高灵敏度和高可靠性的特定 DNA 和 RNA 检测。这些软件包可用于从事核酸扩增的研究机构和实验室。通过检测 SARS-CoV-2 冠状病毒的遗传物质,测试了用于 LAMP 反应的引物组的评估结果,并通过实验证明了使用 LAMPrimers iQ 程序的工作组的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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