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渐进式立体锁定(PSL):一种基于剩余偶极耦合的力场方法,用于确定天然产物和其他小分子的相对构型。

Progressive Stereo Locking (PSL): A Residual Dipolar Coupling Based Force Field Method for Determining the Relative Configuration of Natural Products and Other Small Molecules.

作者信息

Cornilescu Gabriel, Ramos Alvarenga René F, Wyche Thomas P, Bugni Tim S, Gil Roberto R, Cornilescu Claudia C, Westler William M, Markley John L, Schwieters Charles D

机构信息

Pharmaceutical Sciences Division, School of Pharmacy, University of Wisconsin-Madison , Madison, Wisconsin 53705, United States.

Biological Chemistry and Molecular Pharmacology Department, Harvard Medical School , Boston, Massachusetts 02115, United States.

出版信息

ACS Chem Biol. 2017 Aug 18;12(8):2157-2163. doi: 10.1021/acschembio.7b00281. Epub 2017 Jul 12.

Abstract

Establishing the relative configuration of a bioactive natural product represents the most challenging part in determining its structure. Residual dipolar couplings (RDCs) are sensitive probes of the relative spatial orientation of internuclear vectors. We adapted a force field structure calculation methodology to allow free sampling of both R and S configurations of the stereocenters of interest. The algorithm uses a floating alignment tensor in a simulated annealing protocol to identify the conformations and configurations that best fit experimental RDC and distance restraints (from NOE and J-coupling data). A unique configuration (for rigid molecules) or a very small number of configurations (for less rigid molecules) of the structural models having the lowest chiral angle energies and reasonable magnitudes of the alignment tensor are provided as the best predictions of the unknown configuration. For highly flexible molecules, the progressive locking of their stereocenters into their statistically dominant R or S state dramatically reduces the number of possible relative configurations. The result is verified by checking that the same configuration is obtained by initiating the locking from different regions of the molecule. For all molecules tested having known configurations (with conformations ranging from mostly rigid to highly flexible), the method accurately determined the correct configuration.

摘要

确定生物活性天然产物的相对构型是其结构测定中最具挑战性的部分。剩余偶极耦合(RDCs)是核间向量相对空间取向的灵敏探针。我们采用了一种力场结构计算方法,以便对感兴趣的立体中心的R和S构型进行自由采样。该算法在模拟退火协议中使用浮动对齐张量,以识别最符合实验RDC和距离约束(来自NOE和J耦合数据)的构象和构型。具有最低手性角能量和合理对齐张量大小的结构模型的唯一构型(对于刚性分子)或极少数构型(对于刚性较小的分子)被作为未知构型的最佳预测结果给出。对于高度灵活的分子,将其立体中心逐步锁定到其统计上占主导的R或S状态会显著减少可能的相对构型数量。通过检查从分子的不同区域开始锁定是否获得相同的构型来验证结果。对于所有测试的具有已知构型(构象范围从大多刚性到高度灵活)的分子,该方法准确地确定了正确的构型。

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Residual Dipolar Couplings in Structure Determination of Natural Products.天然产物结构测定中的剩余偶极耦合
Nat Prod Bioprospect. 2018 Aug;8(4):279-295. doi: 10.1007/s13659-018-0174-x. Epub 2018 Jun 25.

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