Ion‐Mediated Polymerase Chain Reactions Performed with an Electronically Driven Microfluidic Device |
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| Authors: | Dr Yi Zhang Prof Qian Li Linjie Guo Prof Qing Huang Dr Jiye Shi Dr Yang Yang Prof Dongsheng Liu Prof Chunhai Fan |
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| Institution: | 1. Division of Physical Biology & Bioimaging Center, Shanghai Synchrotron Radiation Facility, CAS Key Laboratory of Interfacial Physics and Technology, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, China;2. Kellogg College, University of Oxford, Oxford, UK;3. UCB Pharma, Slough, UK;4. National Center for NanoScience and Technology (NCNST), Beijing, China;5. Key Laboratory of Organic Optoelectronics & Molecular Engineering of the Ministry of Education, Department of Chemistry, Tsinghua University, Beijing, China |
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| Abstract: | The polymerase chain reaction (PCR) is a powerful method for exponentially amplifying very low amounts of target DNA from genetic, clinical, and forensic samples. However, the heating and cooling steps in PCR largely hamper the miniaturization of thermocyclers for on‐site detection of pathogens and point‐of‐care tests. Herein, we devise an ion‐mediated PCR (IM‐PCR) strategy by exploiting ion‐induced DNA denaturation/renaturation cycles. DNA duplexes are effectively denatured in alkaline solutions; whereas, the denatured single‐stranded DNA strands readily reform duplexes at neutral pH. By using an integrated microchip that can programmably control the solution pH simply switching the potential in a range of several hundred millivolts, we can trigger IM‐PCR at a constant temperature. Analogously to thermal cycling, 30 cycles of pH‐induced denaturation/renaturation were used to amplify protein DNA fragments as confirmed by DNA sequencing. We anticipate that this portable, low‐cost, and scalable IM‐PCR holds great promise for widespread biological, clinical, and environmental applications. |
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| Keywords: | dna amplification isothermal PCR microfluidic devices pH cycling pH-stats |
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