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采用“V”形热循环程序的聚合酶链反应。

Polymerase Chain Reaction using "V" Shape Thermal Cycling Program.

机构信息

Natural Products Research Center, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, P. R. China.

Ethnomedicine College, Chengdu University of Traditional Chinese Medicine; Chengdu 611137, P. R. China.

出版信息

Theranostics. 2019 Feb 28;9(6):1572-1579. doi: 10.7150/thno.31986. eCollection 2019.

DOI:10.7150/thno.31986
PMID:31037124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6485190/
Abstract

Polymerase chain reaction (PCR) is the most commonly used technique in molecular biology and diagnostics. To achieve faster PCR reaction time, two strategies were employed by previous studies. That includes improving the thermal ramp rate by developing novel devices to reduce the time wasted on temperature transitions and cutting the holding time in every step, which could even lead to compromise in amplification efficiency. Hence the need to further improve the technique. : A different way to achieve fast DNA amplification is developed by using the previously thought wasted time spent on heating and cooling the samples to finish the amplification. That means the holding time of the three procedures are omitted and this could be carried out on the ordinary PCR thermal cyclers. : 2/3 of the amplification time is easily saved, compared to the conventionally used method. Additionally, the reaction time could be further reduced by using longer primers with higher melting temperature (Tm). The record time of the "V" shape Polymerase chain reaction (VPCR) conducted on ordinary PCR machine for amplification of a 98 bp fragment is 8 min. Furthermore, VPCR still retains the merits of traditional PCR technique, including specificity, sensitivity, generality, and compatibility with quantitative detection. : It is confirmed that the three procedures of PCR could be completed during the dynamic heating and cooling process when the cyclers are run at a moderate thermal ramp rate. As VPCR described here is based on the current PCR system, it could be implemented in any biological Lab immediately and provide great convenience to the people working in the field of life science and human health.

摘要

聚合酶链式反应(PCR)是分子生物学和诊断学中最常用的技术。为了实现更快的 PCR 反应时间,之前的研究采用了两种策略。这包括通过开发新设备来提高热斜坡率,以减少温度转换浪费的时间,以及缩短每个步骤的保持时间,这甚至可能导致扩增效率降低。因此,需要进一步改进该技术。:通过利用以前认为在加热和冷却样品上浪费的时间来完成扩增,开发了一种实现快速 DNA 扩增的不同方法。这意味着省略了三个步骤的保持时间,并且可以在普通 PCR 热循环仪上进行。:与传统方法相比,很容易节省 2/3 的扩增时间。此外,通过使用具有更高熔点(Tm)的更长引物,可以进一步缩短反应时间。在普通 PCR 机上进行的“V”形聚合酶链反应(VPCR)对 98 bp 片段进行扩增的记录时间为 8 分钟。此外,VPCR 仍然保留了传统 PCR 技术的优点,包括特异性、敏感性、通用性和与定量检测的兼容性。:当循环仪以适度的热斜坡率运行时,确认 PCR 的三个步骤可以在动态加热和冷却过程中完成。由于这里描述的 VPCR 基于当前的 PCR 系统,因此可以立即在任何生物实验室实施,并为从事生命科学和人类健康领域的人们提供极大的便利。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e18d/6485190/03601a78f587/thnov09p1572g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e18d/6485190/86526f86508c/thnov09p1572g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e18d/6485190/03601a78f587/thnov09p1572g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e18d/6485190/86526f86508c/thnov09p1572g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e18d/6485190/03601a78f587/thnov09p1572g002.jpg

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