School of Pharmacy, Xi'an Jiaotong University, 76# Yanta West Road, Xi'an, 710061, China; Institute of Pharmaceutical Science and Technology, Western China Science & Technology Innovation Harbour, Xi'an, 710115, China.
Department of Clinical Pharmacy, Honghui Hospital, Xi'an Jiaotong University, 555# Youyi East Road, Xi'an, 710054, China.
J Chromatogr A. 2023 Mar 29;1693:463903. doi: 10.1016/j.chroma.2023.463903. Epub 2023 Feb 26.
Patients have different responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections and these may be life-threatening for critically ill patients. Screening components that act on host cell receptors, especially multi-receptor components, is challenging. The in-line combination of dual-targeted cell membrane chromatography and a liquid chromatography-mass spectroscopy (LC-MS) system for analyzing angiotensin-converting enzyme 2 (ACE2) and cluster of differentiation 147 (CD147) receptors based on SNAP-tag technology provides a comprehensive solution for screening multiple components in complex samples acting on the two receptors. The selectivity and applicability of the system were validated with encouraging results. Under the optimized conditions, this method was used to screen for antiviral components in Citrus aurantium extracts. The results showed that 25 µmol /L of the active ingredient could inhibit virus entry into cells. Hesperidin, neohesperidin, nobiletin, and tangeretin were identified as antiviral components. In vitro pseudovirus assays and macromolecular cell membrane chromatography further verified the interaction of these four components with host-virus receptors, showing good effects on some or all of the pseudoviruses and host receptors. In conclusion, the in-line dual-targeted cell membrane chromatography LC-MS system developed in this study can be used for the comprehensive screening of antiviral components in complex samples. It also provides new insight into small-molecule drug-receptor and macromolecular-protein-receptor interactions.
患者对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染的反应不同,这可能对重症患者造成生命威胁。筛选作用于宿主细胞受体的药物成分(尤其是多受体成分)具有挑战性。基于 SNAP 标签技术的双靶细胞膜色谱与液相色谱-质谱联用(LC-MS)系统在线联用,为分析血管紧张素转化酶 2(ACE2)和分化簇 147(CD147)受体的药物成分提供了一种综合解决方案,可用于筛选作用于这两个受体的复杂样品中的多种成分。该系统的选择性和适用性已通过令人鼓舞的结果得到验证。在优化条件下,该方法用于筛选枳实提取物中的抗病毒成分。结果表明,25 μmol/L 的有效成分可抑制病毒进入细胞。橙皮苷、新橙皮苷、诺米林和川陈皮素被鉴定为抗病毒成分。体外假病毒实验和大分子细胞膜色谱进一步验证了这四种成分与宿主-病毒受体的相互作用,对某些或所有假病毒和宿主受体均表现出良好的效果。综上所述,本研究建立的在线双靶细胞膜色谱 LC-MS 系统可用于复杂样品中抗病毒成分的综合筛选,为小分子药物-受体和大分子蛋白-受体相互作用提供了新的见解。