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New insight into formation of DNA-containing microparticles during PCR: the scaffolding role of magnesium pyrophosphate crystals
Authors:Vasily N Danilevich  Andrey V Machulin  Alexey V Lipkin  Tatyana V Kulakovskaya  Steven S Smith  Andrey L Mulyukin
Institution:1. Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Science, ul. Miklukho-Maklaya 16/10, Moscow 117997, Russia;2. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Pr. Nauki 5, 142290 Pushchino, Moscow Region, Russia;3. Beckman Research Institute and Division of Urology and Urologic Oncology, City of Hope National Medical Center, 1500 E. Duarte Rd., Duarte, CA 91010, USA;4. Winogradsky Institute of Microbiology, Russian Academy of Science, Pr. 60-letiya Oktyabrya 7/2, Moscow 117312, Russia
Abstract:This work aims to study molecular mechanisms involved in the formation of DNA-containing microparticles and nanoparticles during PCR. Both pyrophosphate and Mg2+ ions proved to play an important role in the generation of DNA microparticles (MPs) with a unique and sophisticated structure in PCR with Taq polymerase. Thus, the addition of Tli thermostable pyrophosphatase to a PCR mixture inhibited this process and caused the destruction of synthesized DNA MPs. Thermal cycling of Na-pyrophosphate (Na-PPi)- and Mg2+-containing mixtures (without DNA polymerase and dNTPs) under the standard PCR regime yielded crystalline oval or lenticular microdisks and 3D MPs composed from magnesium pyrophosphate (Mg-PPi). As shown by scanning electron microscopy (SEM), the produced Mg-PPi microparticles consisted of intersecting disks or their segments. They were morphologically similar but simpler than DNA-containing MPs generated in PCR. The incorporation of dNTPs, primers, or dsDNA into Mg-pyrophosphate particles resulted in the structural diversification of 3D microparticles. Thus, the unusual and complex structure of DNA MPs generated in PCR is governed by the unique feature of Mg-pyrophosphate to form supramolecular particles during thermal cycling. We hypothesize the Mg-pyrophosphate particles that are produced during thermal cycling serve as scaffolds for amplicon DNA condensation.
Keywords:polymerase chain reaction  PCR-generated DNA particles  thermal cycling  magnesium pyrophosphate microparticles  scanning electron microscopy
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