• 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

[通过聚(U)及其盐的无盐溶液的电导率测量得到的电荷密度、大离子迁移率和磷酸基团解离常数的结构参数]

[Structural parameters of charge density, macroion mobility and dissociation constants of the phosphate groups from conductivity measurements of salt free solutions of poly(U) and its salt].

作者信息

Kuznetsov I A, Vorontsova O V, Fabrichnaia O B

出版信息

Mol Biol (Mosk). 1983 Mar-Apr;17(2):392-402.

PMID:6855764
Abstract

Equivalent conductivity (lambda MeP) was studied for the Li+, Na+, K+, Cs+, NH4+ salts of poly(U) and for polyribouridilic acid. Concentration of the salt free solutions of poly(U) ranges from 1 . 10(-4) M-3 . 10(-3) M. Limiting equivalent conductivity (lambda 0 MeP) was obtained based on linear dependence of lambda MeP on Cp1/2 (where Cp is the concentration of nucleic phosphorus). The lambda 0 MeP values obtained were shown to increase linearly with the increase of the limiting mobility of counterion. These data were used to calculate limiting mobility of macroion (lambda p = 43 Ohm-1 Cm2 equiv-1) and parameter xi = 1.13 which characterizes charge density on a macroion. Linear dependence was shown to take place for poly(U) acid and it's salts in the Ostwald's coordinates; moreover, pK value for the phosphate groups is practically independent of the counterion's nature and equal 1.93 +/- 0.32.

摘要

研究了聚(U)的Li⁺、Na⁺、K⁺、Cs⁺、NH₄⁺盐以及聚核糖核酸的当量电导率(λ MeP)。聚(U)无盐溶液的浓度范围为1×10⁻⁴ M至3×10⁻³ M。基于λ MeP对Cp¹/₂(其中Cp是核酸磷的浓度)的线性关系获得了极限当量电导率(λ₀ MeP)。所获得的λ₀ MeP值显示出随着抗衡离子极限迁移率的增加而线性增加。这些数据用于计算大离子的极限迁移率(λp = 43 Ohm⁻¹ Cm² equiv⁻¹)和表征大离子上电荷密度的参数ξ = 1.13。聚(U)酸及其盐在奥斯特瓦尔德坐标中呈现线性关系;此外,磷酸基团的pK值实际上与抗衡离子的性质无关,等于1.93±0.32。

相似文献

1
[Structural parameters of charge density, macroion mobility and dissociation constants of the phosphate groups from conductivity measurements of salt free solutions of poly(U) and its salt].[通过聚(U)及其盐的无盐溶液的电导率测量得到的电荷密度、大离子迁移率和磷酸基团解离常数的结构参数]
Mol Biol (Mosk). 1983 Mar-Apr;17(2):392-402.
2
Polyelectrolyte properties of biopolymers: conductivity and secondary structure of polyriboadenylic acid and its salts in solutions.生物聚合物的聚电解质性质:聚核糖核酸及其盐在溶液中的导电性和二级结构
Biopolymers. 1991 Jan;31(1):65-76. doi: 10.1002/bip.360310107.
3
[Temperature dependence of conductance of isoionic DNA solutions. Determination of dissociation constants of primary phosphoryl groups].[等离子体DNA溶液电导的温度依赖性。一级磷酸基团解离常数的测定]
Mol Biol (Mosk). 1979 May-Jun;13(3):543-9.
4
Thermal denaturation of Na- and Li-DNA in salt-free solutions.无盐溶液中钠-DNA和锂-DNA的热变性
Biopolymers. 1994 Sep;34(9):1275-90. doi: 10.1002/bip.360340915.
5
[Electric conductivity changes in salt-free solutions in connection with the formation of polyriboadenylic and polyribouridylic acid complexes].[与聚核糖腺苷酸和聚核糖尿苷酸复合物形成相关的无盐溶液中的电导率变化]
Biofizika. 1984 Jul-Aug;29(4):560-3.
6
Electric conductivity of aqueous solutions of poly(anetholesulfonic acid) and its alkaline salts.聚(茴香脑磺酸)及其碱性盐的水溶液的电导率。
J Phys Chem B. 2009 Mar 5;113(9):2705-11. doi: 10.1021/jp807518h.
7
Counterion association with native and denatured nucleic acids: an experimental approach.抗衡离子与天然和变性核酸的结合:一种实验方法。
J Mol Biol. 2001 Jul 27;310(5):1011-25. doi: 10.1006/jmbi.2001.4841.
8
Transport properties of some cationic polysaccharides 2. Charge density effect.某些阳离子多糖的传输特性2. 电荷密度效应
J Colloid Interface Sci. 2006 Oct 15;302(2):589-96. doi: 10.1016/j.jcis.2006.06.073. Epub 2006 Jul 20.
9
Polyelectrolyte-macroion complexation in 1:1 and 3:1 salt contents: a Brownian dynamics study.1:1和3:1盐含量下的聚电解质-大离子络合:布朗动力学研究
J Phys Chem B. 2008 Dec 25;112(51):16505-16. doi: 10.1021/jp807596v.
10
Probing hydration of monovalent cations condensed around polymeric nucleic acids.探究聚合核酸周围凝聚的单价阳离子的水合作用。
J Mol Biol. 2004 Aug 6;341(2):551-63. doi: 10.1016/j.jmb.2004.06.015.