对结构的控制和通过Fe (III) 诱导的螺旋体不稳定性的识别
Shiroh Futaki1, Tatsuto Kiwada, Yukio Sugiura
1Institute for Chemical Research, Kyoto University, Uji, Kyoto 611-0011, Japan. futaki@sci.kyoto-u.ac.jp
Journal of the American Chemical Society
|December 2, 2004
概括
研究人员通过酸中使用胺基乙酸 (Ida) 衍生物来证明金属诱导的螺旋体不稳定性. 这种方法为稳定的螺旋提供了功能切换,铁 (III) 触发螺旋不稳定和氧化还原控制,使结构可逆性.
科学领域:
- 生物化学 生物化学
- 材料科学 材料科学 材料科学
- 超分子化学 超分子化学
背景情况:
- 基于的分子设备利用刺激响应的螺旋段进行功能切换.
- 内在稳定的螺旋对受控的形状变化构成挑战.
- 胺基乙酸 (Ida) 衍生物为金属离子介导控制提供了潜力.
研究的目的:
- 为了研究稳定的片段中金属诱导的螺旋体不稳定.
- 探索使用 iminodiacetic 酸 (Ida) 衍生物用于功能切换.
- 为了证明对螺旋构造的氧化还原控制.
主要方法:
- 在特定位置 (i和i+2) 合成含有伊达-氨酸衍生物的17-残留模型.
- 循环二重化谱法用于监测金属离子 (Fe (III) 和Fe (II)) 添加后螺旋内容的变化.
- 使用二氧化二化 (Na2S2O4) 诱导和逆转结构变化的回氧循环实验.
- 在Fe (III) 的存在下对-识别调节的研究.
主要成果:
- 添加铁 (III) 导致模型的螺旋含量显著下降.
- 铁 (II) 不影响螺旋稳定性,表明金属离子特异性.
- 螺旋结构通过铁的氧化还原循环 (Fe(III) 到Fe(II) 和反向可逆控制.
- Fe(III) 调节了Fos和Jun素-拉链片段之间的相互识别.
结论:
- 使用Ida衍生物的金属诱导螺旋不稳定是一种可行的策略,用于稳定系统中的功能切换.
- 该系统具有可回氧切换的特性,允许可逆控制螺旋结构.
- 这种方法在基于的分子设备和响应性材料中具有潜在的应用,包括蛋白质-蛋白质相互作用的调制.
更多相关视频
08:55Methods of Ex Situ and In Situ Investigations of Structural Transformations: The Case of Crystallization of Metallic Glasses
Published on: June 7, 2018
09:06Visualizing Uniaxial-strain Manipulation of Antiferromagnetic Domains in Fe1+YTe Using a Spin-polarized Scanning Tunneling Microscope
Published on: March 24, 2019
相关概念视频
Stereoisomerism
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
Valence Bond Theory
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
Crystal Field Theory - Octahedral Complexes
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Colors and Magnetism
Color in Coordination Complexes
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.
Complexation Equilibria: Factors Influencing Stability of Complexes
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
