Danilevich Vasily N, Artemov Vladimir V, Smith Steven S, Gainutdinov Radmir V, Mulyukin Andrey L
a Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry , Russian Academy of Science , ul. Miklukho-Maklaya 16/10, Moscow , 117997 Russia.
J Biomol Struct Dyn. 2014 Dec;32(12):1979-92. doi: 10.1080/07391102.2013.848411. Epub 2013 Nov 20.
Studies of DNA condensation have opened new perspectives in biotechnology and medicine. DNA condensation induced by polyamines or trivalent metal ions in vitro at room temperature has been investigated in detail. Our recent studies have demonstrated Mg(2+)-mediated formation of DNA condensates during the PCR. In this study, we report the unique morphology and fine structure of PCR-generated condensed DNA particles using electron and atomic force microscopy. The principal morphologies of studied DNA condensates are 3D particles of micrometer dimensions, oval microdisks of nanometer thickness, filaments, and compact nano-sized particles. SEM examinations have revealed a new structural type of spherical and elliptical 3D microparticles formed by numerous definitely oriented microdisks and their segments. AFM revealed a granular structure of the microdisk surface and the smallest nano-sized disks and thinnest nanofibrils - that appear to be the primary products of DNA condensation during the PCR. We suggest that the formation of DNA nanofibrils and nanodisks in PCR occurs due to Mg(2+) - mediated intermolecular (lateral) and intramolecular condensation of ssDNA. Aggregation of elementary nanodisks in the course of thermal PCR cycles, occurring both by magnesium cations and via complementary interactions, give a rise to large nano-sized aggregates and more complex microparticles.
DNA凝聚的研究为生物技术和医学开辟了新的视角。多胺或三价金属离子在室温下体外诱导的DNA凝聚已得到详细研究。我们最近的研究表明,在PCR过程中Mg(2+)介导了DNA凝聚物的形成。在本研究中,我们使用电子显微镜和原子力显微镜报告了PCR产生的凝聚DNA颗粒的独特形态和精细结构。所研究的DNA凝聚物的主要形态是微米级尺寸的三维颗粒、纳米厚度的椭圆形微盘、细丝和致密的纳米级颗粒。扫描电子显微镜检查揭示了一种由许多明确取向的微盘及其片段形成的球形和椭圆形三维微粒的新结构类型。原子力显微镜揭示了微盘表面的颗粒结构以及最小的纳米级盘和最细的纳米纤维——它们似乎是PCR过程中DNA凝聚的主要产物。我们认为,PCR中DNA纳米纤维和纳米盘的形成是由于Mg(2+)介导的单链DNA分子间(横向)和分子内凝聚。在热PCR循环过程中,基本纳米盘通过镁离子和互补相互作用发生聚集,产生大的纳米级聚集体和更复杂的微粒。