• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[锌离子对与偏端霉素形成的DNA复合物作用的光谱表现]

[Spectral manifestations of the effect of Zn2+ ions on DNA complexes with distmycin].

作者信息

Andronikashvili E L, Esipova N G, Kharatishvili M G

出版信息

Biofizika. 1988 Sep-Oct;33(5):767-71.

PMID:3224104
Abstract

Effect of low concentrations of metal bivalent ions on DNA-distamycin complexes was studied. It has been found that when adding small quantity of Zn2- ions the DNA-distamycin complex changes its cooperative properties. A small amount of heavy metal ions incorporated in DNA changes the DNA property to form complexes capable of stimulating the formation of structures of high organization. Thus under the effect of metal small additions both the structure of cellular processes and their regulation are irreversibly simplified, the phase of rest characterized by the maximal number of organization levels of the nuclear apparatus not being reached.

摘要

研究了低浓度二价金属离子对DNA-双间霉素复合物的影响。已发现,当添加少量Zn2+离子时,DNA-双间霉素复合物会改变其协同性质。掺入DNA中的少量重金属离子改变了DNA形成能够刺激高组织结构形成的复合物的性质。因此,在少量金属的作用下,细胞过程的结构及其调节都被不可逆地简化了,静止期也未达到以核装置组织水平数量最多为特征的阶段。

相似文献

1
[Spectral manifestations of the effect of Zn2+ ions on DNA complexes with distmycin].[锌离子对与偏端霉素形成的DNA复合物作用的光谱表现]
Biofizika. 1988 Sep-Oct;33(5):767-71.
2
[Kinetics of the formation of AT-specific DNA-distamin complex].[AT特异性DNA-二胺复合物形成的动力学]
Biofizika. 1986 Sep-Oct;31(5):768-70.
3
[Kinetics of DNA-distaxin complex-formation].[DNA-远曲菌素复合物形成的动力学]
Biofizika. 1987 Jan-Feb;32(1):154-5.
4
[The structure of the complexes of DNA with non-histone chromosomal protein HMGB1 in the presence of manganese ions].
Mol Biol (Mosk). 2004 Nov-Dec;38(6):1041-9.
5
[Synthetic ligands capable of "recognizing" DNA AT-sequences possessing a 2nd-order axis of symmetry].
Dokl Akad Nauk SSSR. 1980 Sep-Oct;254(1):234-8.
6
Analysis of distamycin A binding to UV-damaged DNA.对放线菌素A与紫外线损伤DNA结合的分析。
Nucleic Acids Symp Ser (Oxf). 2004(48):257-8. doi: 10.1093/nass/48.1.257.
7
DNA-binding characteristics of a synthetic analogue of distamycin.
Biochem Biophys Res Commun. 1986 Oct 30;140(2):626-31. doi: 10.1016/0006-291x(86)90777-1.
8
[Oriented complexes of nucleic acids with low-molecular weight ligands. I. Anisotropy of the absorbance of DNA complexes with distamycin A and its analogs].[核酸与低分子量配体的定向复合物。I. 双链霉素A及其类似物与DNA复合物吸光度的各向异性]
Mol Biol (Mosk). 1978 May-Jun;12(3):557-64.
9
[Interaction between DNA and furan-carboxamide analog of antibiotic distamycin A].[DNA与抗生素偏端霉素A的呋喃甲酰胺类似物之间的相互作用]
Mol Biol (Mosk). 1997 Nov-Dec;31(6):1002-11.
10
[Nucleotide sequences in DNA showing preferential binding with distamycin A and acridine derivatives].
Bioorg Khim. 1986 Jun;12(6):764-70.