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      Inhibition of Non-specific Amplification in Loop-Mediated Isothermal Amplification via Tetramethylammonium Chloride

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          Abstract

          Loop-mediated isothermal amplification (LAMP) may be used in molecular and point-of-care diagnostics for pathogen detection. The amplification occurs under isothermal conditions using up to six primers. However, non-specific amplification is frequently observed in LAMP. Non-specific amplification has the potential to be triggered by forward and reverse internal primers. And the relatively low reaction temperature (55–65 °C) induces the secondary structure via primer–primer interactions. Primer redesign and probe design have been recommended to solve this problem. LAMP primers have strict conditions, such as Tm, GC contents, primer dimer, and distance between primers compared to conventional PCR primers. Probe design requires specialized knowledge to have high specificity for a target. In polymerase chain reaction (PCR), some chemicals or proteins are used for improving specificity and efficiency. Therefore, we hypothesized that additives can suppress the non-specific amplification. In this study, tetramethylammonium chloride (TMAC), formamide, dimethyl sulfoxide, Tween 20, and bovine serum albumin have been used as LAMP additives. In our study, TMAC was presented as a promising additive for suppressing non-specific amplification in LAMP.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s13206-022-00070-3.

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          Loop-mediated isothermal amplification of DNA.

          T. Notomi (2000)
          We have developed a novel method, termed loop-mediated isothermal amplification (LAMP), that amplifies DNA with high specificity, efficiency and rapidity under isothermal conditions. This method employs a DNA polymerase and a set of four specially designed primers that recognize a total of six distinct sequences on the target DNA. An inner primer containing sequences of the sense and antisense strands of the target DNA initiates LAMP. The following strand displacement DNA synthesis primed by an outer primer releases a single-stranded DNA. This serves as template for DNA synthesis primed by the second inner and outer primers that hybridize to the other end of the target, which produces a stem-loop DNA structure. In subsequent LAMP cycling one inner primer hybridizes to the loop on the product and initiates displacement DNA synthesis, yielding the original stem-loop DNA and a new stem-loop DNA with a stem twice as long. The cycling reaction continues with accumulation of 10(9) copies of target in less than an hour. The final products are stem-loop DNAs with several inverted repeats of the target and cauliflower-like structures with multiple loops formed by annealing between alternately inverted repeats of the target in the same strand. Because LAMP recognizes the target by six distinct sequences initially and by four distinct sequences afterwards, it is expected to amplify the target sequence with high selectivity.
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            Loop-mediated isothermal amplification (LAMP): principle, features, and future prospects.

            Loop-mediated isothermal amplification (LAMP), a newly developed gene amplification method, combines rapidity, simplicity, and high specificity. Several tests have been developed based on this method, and simplicity is maintained throughout all steps, from extraction of nucleic acids to detection of amplification. In the LAMP reaction, samples are amplified at a fixed temperature through a repetition of two types of elongation reactions occurring at the loop regions: self-elongation of templates from the stem loop structure formed at the 3'-terminal and the binding and elongation of new primers to the loop region. The LAMP reaction has a wide range of possible applications, including point-of-care testing, genetic testing in resource-poor settings (such as in developing countries), and rapid testing of food products and environmental samples.
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              Accelerated reaction by loop-mediated isothermal amplification using loop primers

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                Author and article information

                Contributors
                samkim@gachon.ac.kr
                Journal
                Biochip J
                Biochip J
                Biochip Journal
                The Korean BioChip Society (KBCS) (Seoul )
                1976-0280
                2092-7843
                27 July 2022
                : 1-8
                Affiliations
                GRID grid.256155.0, ISNI 0000 0004 0647 2973, Department of Bionanotechnology, , Gachon University, ; Seongnam, 13120 Republic of Korea
                Author information
                http://orcid.org/0000-0001-9954-0004
                Article
                70
                10.1007/s13206-022-00070-3
                9326409
                35909465
                8a8e9715-5df2-42b5-9cfd-6115dcdb598c
                © The Korean BioChip Society 2022

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 25 May 2022
                : 24 June 2022
                : 7 July 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100002631, Gachon University;
                Award ID: GCU-202008480009
                Award Recipient :
                Funded by: Research Investment for Global Health Technology Fund
                Award ID: RF-TAA-2020-D02
                Award Recipient :
                Categories
                Original Article

                additive,loop-mediated isothermal amplification,non-specific amplification,tetramethylammonium chloride

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