Construction of bio-layer interferometry biosensors via cell-free synthesized proteins for fishing bioactive compounds from Chinese herbs

IF 3.4 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Yanting Wang , Xiaofei Wang , Ningqi Xia , Hao Chen , Linfeng Zhang , Bin Lu , Diya Lv , Yan Cao
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引用次数: 0

Abstract

The application of Bio-Layer Interferometry (BLI) is contingent upon the immobilization of highly purified target proteins onto the sensor. The cumbersome and time-consuming nature of traditional protein expression and purification processes restricts the application of BLI in high-throughput screening of traditional Chinese medicine (TCM). This study aims to develop a rapid and efficient BLI-based platform for screening bioactive components in TCM. An integrated platform combining cell-free protein synthesis (CFPS), BLI, and ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry (UHPLC-QTOF/MS) was established for efficient TCM bioactive compound discovery. Functional C-X-C chemokine receptor 4 (CXCR4) was synthesized in vitro using a CFPS system, which were then validated by surface plasmon resonance (SPR) and western blotting. Immobilized CXCR4 on NTA biosensors enabled BLI-based high-throughput screening of TCM extracts, followed by target-specific compound recovery and characterized via mass spectrometry. Three bioactive TCM constituents were successfully fished and identified as coptisine, ligustilide, and senkyunolide A. All of them exhibited negligible cytotoxicity at concentrations ranging from 6.25 to 100 μM). Furthermore, ligustilide and senkyunolide A demonstrated certain affinity for CXCR4 with KD of 69.86 μM and 14.7 μM, respectively, and significantly inhibited cell migration. This study is the first identification of ligustilide and senkyunolide A as functional ligands of CXCR4. The established CFPS-BLI-UHPLC-QTOF/MS platform enables efficient discovery of low-toxicity, high-affinity CXCR4-targeting therapeutics from TCM.
基于无细胞合成蛋白的生物层干涉测量传感器的构建
生物层干涉法(BLI)的应用取决于高度纯化的目标蛋白在传感器上的固定化。传统的蛋白质表达和纯化过程繁琐、耗时,限制了BLI在中药高通量筛选中的应用。本研究旨在建立一种快速、高效的基于bbi的中药生物活性成分筛选平台。建立了游离蛋白合成(CFPS)、BLI和超高效液相色谱-四极杆飞行时间质谱(UHPLC-QTOF/MS)相结合的中药生物活性化合物高效发现平台。利用CFPS系统体外合成功能性C-X-C趋化因子受体4 (CXCR4),并通过表面等离子体共振(SPR)和western blotting对其进行验证。将CXCR4固定在NTA生物传感器上,实现了基于bli的中药提取物高通量筛选,随后进行了靶向性化合物回收,并通过质谱分析进行了表征。在6.25 ~ 100 μM的浓度范围内,三种具有生物活性的中药成分被成功地捕获并鉴定为黄连碱、藁本内酯和仙丘内酯a。此外,藁本内酯和仙球内酯A对CXCR4表现出一定的亲和力,KD分别为69.86 μM和14.7 μM,并显著抑制细胞迁移。本研究首次鉴定出藁本内酯和仙子内酯A是CXCR4的功能配体。建立的CFPS-BLI-UHPLC-QTOF/MS平台能够高效发现低毒性、高亲和力的中药cxcr4靶向治疗药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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