Strength Of Cation-π Interaction Research Articles

Single-Molecule Force Spectroscopy Reveals Cation-π Interactions in Aqueous Media Are Highly Affected by Cation Dehydration.

Cation-π interactions underlie many important processes in biology and materials science. However, experimental investigations of cation-π interactions in aqueous media remain challenging. Here, we studied the cation-π binding strength and mechanism by pulling two hydrophobic polymers with distinct cation binding properties, i.e., poly-pentafluorostyrene and polystyrene, in aqueous media using single-molecule force spectroscopy and nuclear magnetic resonance measurement. We found that the interaction strengths linearly depend on the cation concentrations, following the order of Li^{+}<NH_{4}^{+}<Na^{+}<K^{+}. The binding energies are 0.03-0.23 kJ mol^{-1} M^{-1}. This order is distinct from the strength of cation-π interactions in gas phase and may be caused by the different dehydration ability of the cations. Taken together, our method provides a unique perspective to investigate cation-π interactions under physiologically relevant conditions.

Influence of sulfamethazine (SMT) on the adsorption of antimony by the black soil: Implication for the complexation between SMT and antimony

This paper reported when sulfamethazine (SMT) and antimony (Sb(V)) coexisted in aqueous solution at pH of 3.0, 5.0 and 7.0, the complexation between SMT and Sb(V) occurred. Such a complexation impeded the adsorption of Sb(V) on the black soil. The higher the solution pH value was, the more the amount of Sb(V) was prevented from adsorbing on the black soil. The maximum adsorption capacity (qm) of Sb(V) at the presence of SMT under pH of 3.0, 5.0 and 7.0 was 5.28, 3.45 and 1.95 mg/g, respectively. -NH2, NH, SO and CN of pyrimidine ring carried by SMT acted as the complexation sites with Sb(V). The complexation constant K were − 3.15, −3.26 and − 3.48 at pH of 7.0, 5.0 and 3.0, respectively, indicating that the complexation strength between SMT and Sb(V) followed the order of pH 7.0 > pH 5.0 > pH 3.0. The binding energy between Sb(V) and the CN group of pyrimidine ring was the highest (1.42 eV), and then followed by the groups of -NH (1.37 eV), SO (0.66 eV) and -NH2 (0.39 eV). Besides SO and CN, Sb(V) tends to complex with NH via coordination bond at pH of 7.0 while -NH2 via cation-π interaction at pH 3.0 and 5.0. Compared to pH of 5.0, the strength of cation-π interaction at pH of 3.0 weakened according to the molecular electrostatic potential map. These results demonstrated that different from the situation where Sb(V) exists in aqueous solution alone, the coexistence of SMT with Sb(V) affected the adsorption behavior of Sb(V) in soil and solution pH was also an influence factor. These findings in this paper would be helpful for further understanding the mobility, bioavailability and other environmental behavior of Sb(V) in soil when Sb(V) coexists with antibiotics even other organic compounds.

Ortho-7 bound to the active-site gorge of free and OP-conjugated acetylcholinesterase: cation-π interactions.

Despite the immense importance of cation-π interactions prevailing in bispyridinium drug acetylcholinesterase (AChE) complexes, a precise description of cation-π interactions at molecular level has remained elusive. Here, we consider a bispyridinium drug, namely, ortho-7 in three different structures of AChE, with and without complexation with organophosphorus (OP) compounds for detailed investigation using all atom molecular dynamics simulation. By quantum mechanical calculations, Y72, W86, Y124, W286, Y337, and Y341 aromatic residues of the enzyme are investigated for possible cation-π interactions with ortho-7. The cation-π interactions in each of the protein-drug complexes are studied using distance, angle, a suitable functional form of them, and electrostatic criteria. The variation of cation-π functional is remarkably consistent with that of the Columbic variation. It is clearly observed that cation-π interactions for some of the residues in the catalytic active site (CAS) and peripheral anionic site (PAS) of the enzyme are either enhanced or reduced based on the nature of OP conjugation (i.e., nerve gas, tabun or pesticide, fenamiphos) when compared with the OP-free enzyme. The strength of cation-π interaction is strongly dependent on the type OP conjugation. The effect of conjugation at CAS is also seen to influence the cation-π interaction at the PAS region. The variation of cation-π interactions on the type of conjugating OP compounds might be suggestive of a reason as to why wide spectrum drug against any OP poisoning is yet to arrive in the market.

3P054 タンパク質中におけるカチオン-π相互作用の強さの評価(蛋白質-物性(安定性,折れたたみなど),第48回日本生物物理学会年会)

3P054 タンパク質中におけるカチオン-π相互作用の強さの評価(蛋白質-物性(安定性,折れたたみなど),第48回日本生物物理学会年会)