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MTD-PLS: A PLS variant of the minimal topologic difference method. III. Mapping interactions between estradiol derivatives and the alpha estrogenic receptor

机译:MTD-PLS:最小拓扑差异方法的PLS变体。三,雌二醇衍生物与α雌激素受体之间的相互作用

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摘要

A homogeneous collection of 45 estrogen agonist derivatives with relative binding affinities measured to the estrogen receptor from Ratus norvegicus was used. The quantitative structure-activity relationships were derived using an improved minimal topologic difference (MTD) method in a partial least-squares (PLS) variant. The spatially assigned analysis of fragment properties can provide receptor site maps, within the limits of the existing series. A steric misfit was found for the steroidal position 2; benefic hydrophobic and van der Waals (enhanced by high polarizability) interactions were found for the 17 alpha-CH=CH-X group. MTD-PLS mapping results are confirmed by the experimentally derived estradiol-estrogen receptor binding site contacts (based on X-ray crystallography). Our results suggest that this MTD-PLS method can yield useful results for interactions with receptors of unknown 3D structure and, generally, for the steric rigidity of receptor sites.
机译:使用45种雌激素激动剂衍生物的同质集合,该衍生物具有相对于来自Ratus norvegicus的雌激素受体的相对结合亲和力。使用改进的最小拓扑差异(MTD)方法在偏最小二乘(PLS)变量中得出定量的结构活性关系。在现有序列的范围内,对片段特性进行空间分配的分析可以提供受体位点图。发现甾体位置2的空间不匹配;在17个α-CH= CH-X基团中发现了有益的疏水和范德华相互作用(通过高极化率增强)。通过实验得出的雌二醇-雌激素受体结合位点接触(基于X射线晶体学)证实了MTD-PLS作图结果。我们的结果表明,这种MTD-PLS方法可以产生与未知3D结构的受体相互作用的有用结果,并且通常可以产生受体位点的空间刚性。

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