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将猪胰腺脂肪酶固定在金属有机骨架上,PPL@MOF:从天然草药中发现有效配体的新平台。

Immobilization of porcine pancreatic lipase onto a metal-organic framework, PPL@MOF: A new platform for efficient ligand discovery from natural herbs.

机构信息

State Key Laboratory of Natural Medicines, Jiangsu Key Laboratory of Bioactive Natural Product Research, School of Traditional Chinese Pharmacy, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing, 210009, PR China.

State Key Laboratory of Natural Medicines, Jiangsu Key Laboratory of Bioactive Natural Product Research, School of Traditional Chinese Pharmacy, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing, 210009, PR China.

出版信息

Anal Chim Acta. 2020 Feb 22;1099:94-102. doi: 10.1016/j.aca.2019.11.042. Epub 2019 Nov 22.

Abstract

In terms of ligand fishing, the amount and the relative activity recovery of enzymes immobilized on magnetic particles and nanoparticles are not preeminent. Therefore, the metal-organic framework (MOF) UiO-66-NH was synthesized to immobilize the porcine pancreatic lipase (PPL) via precipitation-cross-linking, and the resulting novel biological matrices named PPL@MOF manifested high PPL loading capacity (98.31 mg/g) and relative activity recovery (104.4%). Moreover, the novel enzyme-MOF composite was applied to screen lipase inhibitors from Prunella vulgaris L. to enrich and improve the techniques of ligand fishing. As a result, 13 lipase ligands were obtained, and 12 compounds were determined by HPLC-Q-TOF-MS/MS. All of these ligands were further confirmed to be potential inhibitors through the verification of the activity assay and molecular docking. The proposed approach based on PPL@MOF was superior in terms of abundant protein loading capacity, high enzyme catalytic activity and easy preparation process. Taken together, our newly developed method provided a new platform for efficient discovering bioactive molecules from natural herbs.

摘要

就配体捕捞而言,固定在磁性颗粒和纳米颗粒上的酶的数量和相对活性回收率并不突出。因此,合成了金属有机骨架(MOF)UiO-66-NH 以通过沉淀交联固定猪胰腺脂肪酶(PPL),所得新型生物基质命名为 PPL@MOF,其具有高 PPL 负载能力(98.31mg/g)和相对活性回收率(104.4%)。此外,新型酶-MOF 复合材料被应用于从夏枯草中筛选脂肪酶抑制剂,以丰富和改进配体捕捞技术。结果,从夏枯草中获得了 13 种脂肪酶配体,通过 HPLC-Q-TOF-MS/MS 确定了 12 种化合物。所有这些配体都通过活性测定和分子对接的验证进一步证实为潜在的抑制剂。基于 PPL@MOF 的方法在丰富的蛋白质负载能力、高酶催化活性和易于制备过程方面具有优势。总之,我们新开发的方法为从天然草药中高效发现生物活性分子提供了一个新的平台。

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