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Protein-Sized Quantum Dot Luminescence Can Distinguish between 'Straight', 'Bent', and 'Kinked' Oligonucleotides

机译:蛋白质大小的量子点发光可以区分“直”,“弯曲”和“扭结”寡核苷酸

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摘要

There is increasing evidence from X-ray crystal structures, gel electrophoresis, enzyme cyclization, and electron microscopy experiments that DNA sequence can dictate overall DNA structure. In particular, double-stranded DNAs that contain 5′-A_n-3′ (where n = 3-7) phased one full double-helical twist apart appear to induce curvature in the context of a long strand (~10~2 bp) of DNA in gel mobility and enzyme cyclization experiments. The sequence 5′-d(CATGGCCATG)-3′ has been crystallized as a self-complementary duplex and shows a definite kink of 23° across the central 5′-GGCC-3′. However, packing forces and the presence of highly-charged counterions might also influence the DNA structure in the solid state. Here we describe a novel method for probing DNA structure in dilute solution: the adsorption of oligonucleotides of defined sequence to protein-sized particles. The particles are "quantum dots" of the semiconductor CdS, and we find that the surface-sensitive luminescence of these particles can discriminate between "straight", "bent", and "kinked" oligonucleotides in dilute solution.
机译:从X射线晶体结构,凝胶电泳,酶环化和电子显微镜实验中,越来越多的证据表明DNA序列可以决定总体DNA结构。特别是,包含5'-A_n-3'(其中n = 3-7)相距一个完整的双螺旋扭曲的双链DNA在长链(〜10〜2 bp)的情况下似乎会诱导弯曲。 DNA在凝胶迁移率和酶环化实验中的应用序列5'-d(CATGGCCATG)-3'已结晶为自互补双链体,并且在中心5'-GGCC-3'上显示出23°的明确扭结。但是,堆积力和高电荷抗衡离子的存在也可能会影响固态的DNA结构。在这里,我们描述了一种在稀溶液中探测DNA结构的新方法:将定义序列的寡核苷酸吸附到蛋白质大小的颗粒上。粒子是半导体CdS的“量子点”,我们发现这些粒子的表面敏感发光可以区分稀溶液中的“纯”,“弯曲”和“扭结”寡核苷酸。

著录项

  • 来源
    《Journal of the American Chemical Society》 |1995年第35期|p.9099-9100|共2页
  • 作者单位

    Department of Chemistry and Biochemistry University of South Carolina Columbia, South Carolina 29208;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

  • 入库时间 2022-08-18 03:26:22

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