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钙离子载体A23187及其氨基酸复合物:光谱学与分子建模研究

Calcium ionophore, A23187 and its amino acid complexes: spectroscopic and molecular modeling studies.

作者信息

Namboodiri K, Gaber B P, Easwaran K R, Balasubramanian S V

机构信息

Center for Bio-Molecular Science and Engineering, Naval Research Laboratory, Washington, D.C. 20375.

出版信息

J Biomol Struct Dyn. 1994 Apr;11(5):913-26. doi: 10.1080/07391102.1994.10508044.

Abstract

The circular dichroism, fluorescence, Nuclear Magnetic Resonance and BLM conductance studies indicate that A23187 forms a stable complex with amino acids at low ionophore concentrations (< 10(-4)M). However, A23187 prefers to be in a dimeric structure with no significant binding to amino acids, at concentrations higher than 10(-4)M. It was also observed that at lower concentrations, at which the amino acids bind to the ionophore, the affinity for calcium ions was several orders of magnitude lower than that at higher ionophore concentrations. We have also conducted molecular modeling studies to examine the structure of the A23187 dimer and its amino acid complexes. The results of these modeling studies strongly support our experimental results and validate the formation of a hydrogen bonded and energetically stable A23187 dimer and its amino acid complexes.

摘要

圆二色性、荧光、核磁共振和BLM电导研究表明,在低离子载体浓度(<10^(-4)M)下,A23187与氨基酸形成稳定的复合物。然而,在高于10^(-4)M的浓度下,A23187更倾向于形成二聚体结构,且与氨基酸无明显结合。还观察到,在氨基酸与离子载体结合的较低浓度下,对钙离子的亲和力比在较高离子载体浓度下低几个数量级。我们还进行了分子建模研究,以研究A23187二聚体及其氨基酸复合物的结构。这些建模研究的结果有力地支持了我们的实验结果,并验证了氢键结合且能量稳定的A23187二聚体及其氨基酸复合物的形成。

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