Howard James R, Shuluk Julia R, Bhakare Arya, Anslyn Eric V
Department of Chemistry, The University of Texas at Austin, Austin, TX 78705 (USA).
Lead contact.
Chem. 2024 Jul 11;10(7):2074-2088. doi: 10.1016/j.chempr.2024.05.009. Epub 2024 Jun 12.
Circular dichroism (CD) based enantiomeric excess (ee) determination assays are optical alternatives to chromatographic ee determination in high-throughput screening (HTS) applications. However, the implementation of these assays requires calibration experiments using enantioenriched materials. We present a data-driven approach that circumvents the need for chiral resolution and calibration experiments for an octahedral Fe(II) complex (1) used for the ee determination of α-chiral primary amines. By computationally parameterizing the imine ligands formed in the assay conditions, a model of the circular dichroism (CD) response of the Fe(II) assembly was developed. Using this model, calibration curves were generated for four analytes and compared to experimentally generated curves. In a single-blind ee determination study, the ee values of unknown samples were determined within 9% mean absolute error, which rivals the error using experimentally generated calibration curves.
基于圆二色性(CD)的对映体过量(ee)测定法是高通量筛选(HTS)应用中色谱ee测定的光学替代方法。然而,这些测定法的实施需要使用对映体富集材料进行校准实验。我们提出了一种数据驱动的方法,该方法无需对用于α-手性伯胺ee测定的八面体Fe(II)配合物(1)进行手性拆分和校准实验。通过在计算上对测定条件下形成的亚胺配体进行参数化,建立了Fe(II)组装体的圆二色性(CD)响应模型。使用该模型,为四种分析物生成了校准曲线,并与实验生成的曲线进行了比较。在一项单盲ee测定研究中,未知样品的ee值在平均绝对误差9%以内被测定,这与使用实验生成的校准曲线的误差相当。