Holo-Ni ((II) HpNikRは2つの異なるニッケル結合部位を含む非対称なテトラメールです
Abby L West1, Franz St John, Pedro E M Lopes
1Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, Maryland 21201-1180, USA.
Journal of the American Chemical Society
|September 25, 2010
まとめ
ヘリコバクター・パイロリ菌の金属調節タンパク質NikRは,2つの異なる方法でニッケルイオンを結合します. ニッケル結合型HpNikRに関するこの構造的洞察は,そのDNA結合特異性を説明するかもしれない.
科学分野:
- 構造生物学 構造生物学とは
- バイオケミストリー バイオケミストリー
- メタロプロテイン (metalloprotein) とは
背景:
- ヘリコバクター・パイロリ・ニークR (HpNikR) は,ニッケルの存在に基づいて遺伝子発現を制御する金属調節性タンパク質です.
- HpNikRのニッケル結合メカニズムを理解することは,その規制機能を明らかにするために不可欠です.
研究 の 目的:
- Ni(II) HpNikR.の結晶構造を決定するために.
- HpNikR.内のニッケル調整環境を調査する.
主な方法:
- ホロ HpNikR.のX線結晶学 (2.37 Å解像度)
- 密度関数理論 (DFT) による計算.
主要な成果:
- 構造は,2つの異なる調整環境の4つのニッケルイオンを明らかにします.
- 2つのニッケルイオンは,予測された4座標の正方形平面幾何学を採用します.
- 2つのニッケルイオンは,ヒスティジンの残留物と水分子を含む予期せぬ5または6座標の幾何学を示します.
- DFTの計算は,5/6座標の幾何学のエネルギー優位性を示しています.
結論:
- HpNikRはニッケル調整部位が独特で,ある部位の幾何学がエネルギー的に有利である.
- 異なるニッケル調整環境の存在は,HpNikRのDNA結合特異性と親和性に影響する可能性がある.
- この構造的特徴は,ニッケル依存遺伝子調節におけるHpNikRの役割を理解するための基礎を提供します.
関連する概念動画
Structural Isomerism
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...
Metal-Ligand Bonds
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
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 - Tetrahedral and Square Planar Complexes
Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Cooperative Allosteric Transitions
Cooperative allosteric transitions can occur in multimeric proteins, where each subunit of the protein has its own ligand-binding site. When a ligand binds to any of these subunits, it triggers a conformational change that affects the binding sites in the other subunits; this can change the affinity of the other sites for their respective ligands. The ability of the protein to change the shape of its binding site is attributed to the presence of a mix of flexible and stable segments in the...


![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)