Jiangsu Key Laboratory of TCM Evaluation and Translational Research, China Pharmaceutical University, Nanjing 211198, PR China.
Jiangsu Key Laboratory of TCM Evaluation and Translational Research, China Pharmaceutical University, Nanjing 211198, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2022 Apr 15;1195:123203. doi: 10.1016/j.jchromb.2022.123203. Epub 2022 Mar 2.
Some natural products are important sources of treatments for hypertension based on their potential inhibitory effects on angiotensin-converting enzyme (ACE); however, it is difficult to identify natural ACE inhibitors (ACEIs) due to the complex secondary metabolite environment of natural products. Enzyme immobilization is an important method for screening active constituents in natural products, but this method can sometimes return false-positive and false-negative results. To improve the accuracy and reliability of ligand-fishing methods, we established a novel strategy based on enzyme-immobilized ligand fishing combined with active-site blocking and directional enrichment technologies. We first synthesized ACE-immobilized mesoporous magnetic beads and then verified the screened compounds by molecular docking and in vitro activity detection. We then used active-site blocking to exclude non-specific binding constituents and applied directional enrichment to enrich the low-content constituents for ligand fishing. The screening identified six potential ACEIs from Scutellariae Radix and eight potential ACEIs from Lonicerae japonicae flos, and their inhibitory activity was confirmed by molecular docking simulations and in vitro activity detection. This process screened six additional compounds and excluded two false-positive results as compared with results exclusively using enzyme immobilization. This strategy provides a feasible method for screening active compounds in natural products.
一些天然产物因其对血管紧张素转化酶(ACE)的潜在抑制作用而成为治疗高血压的重要来源,但由于天然产物的复杂次生代谢环境,很难识别天然 ACE 抑制剂(ACEIs)。酶固定化是筛选天然产物中活性成分的重要方法,但该方法有时会返回假阳性和假阴性结果。为了提高配体捕捞方法的准确性和可靠性,我们建立了一种基于酶固定化配体捕捞结合活性位点阻断和定向富集技术的新策略。我们首先合成了 ACE 固定化介孔磁性珠,然后通过分子对接和体外活性检测来验证筛选出的化合物。然后,我们使用活性位点阻断排除非特异性结合成分,并应用定向富集富集低含量成分进行配体捕捞。筛选从黄芩中鉴定出 6 种潜在的 ACEIs,从金银花中鉴定出 8 种潜在的 ACEIs,并通过分子对接模拟和体外活性检测证实了它们的抑制活性。与仅使用酶固定化相比,该过程筛选出了另外 6 种化合物,并排除了 2 种假阳性结果。该策略为筛选天然产物中的活性化合物提供了一种可行的方法。