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相关概念视频

Stereoisomerism02:52

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...
Proton (¹H) NMR: Chemical Shift01:07

Proton (¹H) NMR: Chemical Shift

Organic molecules primarily contain carbon and hydrogen atoms. While all the hydrogen isotopes are NMR-active, protium or hydrogen-1 is the most abundant. It has a significant energy separation between its nuclear spin states due to its large gyromagnetic ratio. As per Boltzmann's distribution, an increase in the energy separation implies a greater excess population of nuclei available for excitation, resulting in a strong NMR absorption signal.
Absorption signals of all the protium nuclei in a...
¹H NMR: Complex Splitting01:13

¹H NMR: Complex Splitting

A proton M that is coupled to a proton X results in doublet signals for M. However, NMR-active nuclei can be simultaneously coupled to more than one nonequivalent nucleus. When M is coupled to a second proton A, such as in styrene oxide, each peak in the doublet is split into another doublet.
Splitting diagrams or splitting tree diagrams are routinely used to depict such complex couplings. While drawing splitting diagrams, the splitting with the larger coupling constant is usually applied first.
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)01:20

¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)

When proton-coupled carbon-13 spectra are simplified by a broadband proton decoupling technique, structural information about the coupled protons is lost. Distortionless enhancement by polarization transfer (DEPT) is a technique that provides information on the number of hydrogens attached to each carbon in a molecule. While the DEPT experiment utilizes complex pulse sequences, the pulse delay and flip angle are specifically manipulated. The resulting signals have different phases depending on...
¹H NMR Chemical Shift Equivalence: Homotopic and Heterotopic Protons01:03

¹H NMR Chemical Shift Equivalence: Homotopic and Heterotopic Protons

Protons in identical electronic environments within a molecule are chemically equivalent and have the same chemical shift. The replacement test is a useful tool to identify chemical equivalence and predict NMR spectra. A substituent replaces each of the protons being examined and the resulting molecules are compared. If the same molecule is obtained, the protons are equivalent or homotopic. Replacement of any hydrogens in ethane by chlorine yields chloroethane because all six protons are...
Insensitive Nuclei Enhanced by Polarization Transfer (INEPT)01:15

Insensitive Nuclei Enhanced by Polarization Transfer (INEPT)

Insensitive Nuclei Enhanced by Polarization Transfer (INEPT) is an advanced Nuclear Magnetic Resonance (NMR) technique specifically designed to detect and enhance the signals of low-abundance nuclei, such as carbon-13 and nitrogen-15, in small molecules. The fundamental principle behind INEPT is the transfer of polarization from a more abundant and highly polarizable nucleus, typically hydrogen-1, to the low-abundance nucleus of interest. This process effectively boosts the NMR signal of the...

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Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy
14:55

Atomic Scale Structural Studies of Macromolecular Assemblies by Solid-state Nuclear Magnetic Resonance Spectroscopy

Published on: September 17, 2017

通过prolyl imide键Cis/Trans异构化在Itk SH2域中调节的配体特异性:一个定量NMR研究.

Patrick J Breheny1, Alain Laederach, D Bruce Fulton

  • 1Department of Biochemistry, Biophysics and Molecular Biology, Program of Bioinformatics and Computational Biology, Iowa State University, Ames, Iowa 50011, USA.

Journal of the American Chemical Society
|December 18, 2003
PubMed
概括

介素-2 氨酸激酶 (Itk) SH2 域使用 cis/trans 异体化来结合不同的配体. 这项研究量化了亲和关系,揭示了对SH3域和类联体的明显偏好.

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科学领域:

  • 生物化学 生物化学
  • 分子生物学分子生物学
  • 结构生物学 结构生物学

背景情况:

  • 介素二氨酸激酶 (Itk) Src同质性2 (SH2) 域结合了含有氨酸的和Itk Src同质性3 (SH3) 域.
  • 联体结合特异性是由Itk SH2域内的Asn286-Pro287胺基键的cis/trans异构化调节的.

研究的目的:

  • 开发和应用一种新的方法来量化对Itk SH2域的不同对象的联体亲属性.
  • 阐明Itk SH2域的cis和trans conformers对其已知的连接体的差异性结合亲和力.

主要方法:

  • 使用化学转移扰动和交叉峰值体积分析.
  • 测量了基和Itk SH3域与Itk SH2域的cis和trans conformers的结合亲和力.

主要成果:

  • 与变压体相比,cis imide 结合器对 Itk SH3 域的亲和力是 3.5 倍的.
  • 变态变体表现出比cis变体对脂联体的4倍的亲和力.

结论:

  • 这项研究量化地证明了Itk SH2域对象的差异性联体结合特异性.
  • 开发的方法提供了一种一般方法,用于分析具有分子开关的结构异质系统.