Noncovalent cation-π interactions - their role in nature

被引:6
|
作者
Fink, Krzysztof [1 ]
Boratynski, Janusz [1 ]
机构
[1] PAN Ludwika Hirszfelda, Inst Immunol & Terapii Doswiadczalnej, Lab Chem Biomed Neolek, PL-53114 Wroclaw, Poland
关键词
non-covalent interactions; cation-pi interactions; ALPHA-HELICAL PEPTIDES; AROMATIC-AMINO-ACIDS; SOLID-STATE NMR; BINDING PROTEINS; STRUCTURAL BASIS; SODIUM-CHANNELS; SIDE-CHAINS; GAS-PHASE; NICOTINIC RECEPTOR; MOLECULAR-DYNAMICS;
D O I
10.5604/17322693.1127950
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Non-covalent interactions play an extremely important role in organisms. The main non-covalent interactions in nature are: ion-ion interactions, dipole-dipole interactions, hydrogen bonds, and van der Waals interactions. A new ldnd of intermolecular interactions - cation-pi interactions - is gaining increasing attention. These interactions occur between a cation and a pi system. The main contributors to cation-pi interactions are electrostatic, polarization and, to a lesser extent, dispersion interactions. At first, cation-pi interactions were studied in a gas phase, with metal cationaromatic system complexes. The characteristics of these complexes are as follows: an increase of cation atomic number leads to a decrease of interaction energy, and an increase of cation charge leads to an increase of interaction energy. Aromatic amino acids bind with metal cations mainly through interactions with their main chain. Nevertheless, cation-pi interaction with a hydrophobic side chain significantly enhances binding energy. In water solutions most cations preferentially interact with water molecules rather than aromatic systems. Cation-pi interactions occur in environments with lower accessibility to a polar solvent. Cation-pi interactions can have a stabilizing role on the secondary, tertiary and quaternary structure of proteins. These interactions play an important role in substrate or ligand binding sites in many proteins, which should be taken into consideration when the screening of effective inhibitors for these proteins is carried out. Cation-pi interactions are abundant and play an important role in many biological processes.
引用
收藏
页码:1276 / 1286
页数:11
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