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利用磁性分子印迹聚合物作为人工抗体,从草药中高效发现和捕获新型神经元型一氧化氮合酶-突触后密度蛋白-95 解偶联剂。

Efficient discovery and capture of new neuronal nitric oxide synthase-postsynaptic density protein-95 uncouplers from herbal medicines using magnetic molecularly imprinted polymers as artificial antibodies.

机构信息

School of Pharmacy, Nanjing Medical University, Nanjing, China.

Tang Center for Herbal Medicine Research, and Department of Anesthesia and Critical Care, University of Chicago, Chicago, IL, USA.

出版信息

J Sep Sci. 2017 Sep;40(17):3522-3534. doi: 10.1002/jssc.201700595.

DOI:10.1002/jssc.201700595
PMID:28704580
Abstract

In the scope of stroke treatment, new neuronal nitric oxide synthase-postsynaptic density protein-95 uncouplers from herbal medicines were discovered and captured. To do so, highly selective magnetic molecularly imprinted polymers with a core-shell structure were prepared as artificial antibodies. According to the results of computational simulations, we designed and synthesized various polymers with varying amounts and types of template, functional monomer, cross-linker, and solvent. Characterization and performance tests revealed that the most appropriate artificial antibodies showed uniform spherical morphologies, large adsorption capacities, fast-binding kinetics, high selectivity, and quick separation. These artificial antibodies were then used as sorbents for dispersive magnetic solid-phase extraction coupled with high-performance liquid chromatography and mass spectrometry to capture and identify structural analogs to ZL006 from extracts of Scutellariae radix, Psoraleae fructus, and Trifolium pratense. Furthermore, according to the neuroprotective effect and coimmunoprecipitation test, Baicalein, Neobavaisoflavone, Corylifol A, and Biochanin A can be the potential uncouplers of neuronal nitric oxide synthase-postsynaptic density protein-95. Therefore, this present study contributes valuable information for the discovery of neuronal nitric oxide synthase-postsynaptic density protein-95 uncouplers from herbal medicines.

摘要

在脑卒中治疗领域,从草药中发现并提取了新型的神经元型一氧化氮合酶-突触后密度蛋白-95 解偶联剂。为此,我们制备了具有核壳结构的高度选择性磁性分子印迹聚合物作为人工抗体。根据计算模拟的结果,我们设计并合成了各种具有不同模板、功能单体、交联剂和溶剂用量和类型的聚合物。特性和性能测试表明,最合适的人工抗体具有均匀的球形形态、较大的吸附容量、快速的结合动力学、高选择性和快速的分离。然后,这些人工抗体被用作分散式磁性固相萃取的吸附剂,与高效液相色谱和质谱联用,从黄芩、补骨脂和三叶草的提取物中捕获和鉴定 ZL006 的结构类似物。此外,根据神经保护作用和共沉淀试验,黄芩素、新大豆苷元、山柰酚和大豆苷元 A 可能是神经元型一氧化氮合酶-突触后密度蛋白-95 的潜在解偶联剂。因此,本研究为从草药中发现神经元型一氧化氮合酶-突触后密度蛋白-95 解偶联剂提供了有价值的信息。

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