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汞(II)与聚(dG-dC)复合物的结构形式及转变

Structural forms and transitions for the complex of mercury(II) with poly(dG-dC).

作者信息

Keller P B, Hartman K A

机构信息

Department of Biochemistry and Biophysics, University of Rhode Island, Kingston 02881.

出版信息

J Biomol Struct Dyn. 1987 Jun;4(6):1013-26. doi: 10.1080/07391102.1987.10507694.

Abstract

Infrared spectroscopy was used to study hydrated double-helical poly(dG-dC) complexed with varying amounts of mercury(II). For one Hg(II) per ten nucleotide residues (r = 0.1), the B structure was stabilized and the B* structure was absent at high hydration. The Z structure did not form as hydration was reduced. For r = 0.2, the B and Z structures coexisted at high hydration and the transition to total Z structure was broad as hydration was reduced. Hg(II) was bound exclusively to the guanine residues probably at N3 or N7 for r less than or equal to 0.25. The cytosine residue did not protonate (at N3) as Hg(II) was bound to guanine. The addition of NaCl together with Hg(II) reduced the binding of Hg(II), stabilized the B structure at the highest hydration and caused a sharp transition between the B and Z structures as hydration was lowered. Hydration with D2O stabilized the Z structure for poly(dG-dC) complexed with HgCl2.

摘要

采用红外光谱法研究了与不同量汞(II)络合的水合双链聚(dG-dC)。对于每十个核苷酸残基中有一个Hg(II)(r = 0.1),B结构得以稳定,在高水合度下不存在B*结构。随着水合度降低,Z结构未形成。对于r = 0.2,在高水合度下B结构和Z结构共存,随着水合度降低,向完全Z结构的转变较为宽泛。当r小于或等于0.25时,Hg(II)仅与鸟嘌呤残基结合,可能是在N3或N7位。当Hg(II)与鸟嘌呤结合时,胞嘧啶残基不会质子化(在N3位)。NaCl与Hg(II)一起添加会降低Hg(II)的结合,在最高水合度下稳定B结构,并在水合度降低时导致B结构和Z结构之间的急剧转变。用D2O水合可使与HgCl2络合的聚(dG-dC)的Z结构稳定。

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