天然产物研究与开发 ›› 2025, Vol. 37 ›› Issue (11): 2102-2112.doi: 10.16333/j.1001-6880.2025.11.014 cstr: 32307.14.1001-6880.2025.11.014

• 开发研究 • 上一篇    下一篇

一种鳄嘴花源多肽的改造及体外抗炎活性研究

朱方莉1,何炳蔚2,曲丽萍2,3*   

  1. 1上海贝泰妮生物科技有限公司,上海200335;2云南贝泰妮生物科技集团股份有限公司;3云南云科特色植物提取实验室有限公司,昆明650106
  • 出版日期:2025-11-27 发布日期:2025-11-26
  • 基金资助:
    云南特色植物筛选与研发服务CXO平台建设(2022YKZY001);云南特色植物新原料自主研发及产业化(2023YKZY004)

Study on modification and in vitro inflammation activity of Clinacanthus nutans (Burm.f.) Lindau peptides

ZHU Fang-li1,HE Bing-wei2,QU Li-ping2,3 *   

  1. 1Shanghai Botanee Bio-technology Co.,Ltd.,Shanghai 200335,China;2China Yunnan Botanee Bio-technology Group Co.,Ltd.;3Yunnan Yunke Characteristic Plant Extraction Laboratory Co.,Ltd.,Kunming 650106,China
  • Online:2025-11-27 Published:2025-11-26

摘要:

探究鳄嘴花(Clinacanthus nutans (Burm. f.) Lindau)中的抗炎活性多肽以及其可能的分子机制。通过碱溶酸沉与超滤技术提取蛋白,筛选出具有抗炎活性的两个组分后,利用液相色谱-质谱联用技术,共鉴定出116条多肽序列。进一步通过活性评分网站和多肽毒性预测筛选出无毒且评分大于0.8的25条多肽。将其与丝裂原活化蛋白激酶(mitogen-activated protein kinase,MAPK)靶点进行分子对接,筛选出3条优于MAPK抑制剂西替利嗪的多肽序列。采用固相合成法合成这3条多肽后,测试其对脂多糖诱导的RAW 264.7细胞炎症的抑制作用,最终发现了具有优异抗炎潜力的多肽序列WDDC。为了避免与人源蛋白重复并提高稳定性,引入了甘氨酸和乙酰基,改造后的多肽命名为Ac-WDDCG。结果显示,Ac-WDDCG能够显著抑制人脐静脉内皮细胞(human umbilical vein endothelial cells,HUVEC)中Nod样受体蛋白3(Nod-like receptor family,NLRP3)信号通路相关基因[Toll样受体4(toll-like receptor 4,TLR4)、NLRP3和核因子-κB(nuclear factor-kappa B,NF-κB)]的mRNA表达(P <0.05),显著降低RAW 264.7细胞炎症模型中下游炎症因子[肿瘤坏死因子-α(tumor necrosis factor-alpha,TNF-α)、白细胞介素-6(interleukin-6,IL-6)和NO]的分泌水平(P <0.01),并减少了CuSO4诱导的斑马鱼中性粒细胞迁移(P <0.05)。提示Ac-WDDCG具有较好的抗炎活性,其机制可能与抑制NLRP3信号通路有关。

关键词: 鳄嘴花, 多肽, 丝裂原活化蛋白激酶, Nod样受体蛋白3信号通路, 炎症因子

Abstract:

The study aimed to explore the anti-inflammatory peptides in Clinacanthus nutans (Burm. f.) Lindau and elucidate their potential molecular mechanisms. Proteins were extracted using alkaline extraction and isoelectric precipitation followed by ultrafiltration techniques. After screening out two fractions with anti-inflammatory activities, a total of 116 polypeptide sequences were identified by using liquid chromatography-mass spectrometry. Subsequent screening using an activity scoring platform and polypeptide toxicity prediction identified 25 non-toxic polypeptide sequences with scores >0.8. Molecular docking with the mitogen-activated protein kinase (MAPK) target identified three polypeptide sequences with superior efficacy compared to the MAPK inhibitor cetirizine. These sequences were synthesized using solid-phase synthesis, and their inhibitory effects on lipopolysaccharide- induced inflammation in RAW 264.7 cells were evaluated. Ultimately, a polypeptide sequence, WDDC, demonstrating significant anti-inflammatory potential, was identified. To minimize redundancy with human proteins and enhance stability, modifications involving glycine and acetyl moieties were implemented, resulting in the designation of the modified polypeptide as Ac-WDDCG. The findings indicated that Ac-WDDCG significantly inhibited the mRNA expression of genes associated with the Nod-like receptor family (NLRP3) signaling pathway, including toll-like receptor 4 (TLR4),NLRP3,and nuclear factor-kappa B(NF-κB) in human umbilical vein endothelial cells (HUVEC cells) (P <0.05).Moreover,it markedly reduced the secretion levels of downstream inflammatory mediators,including tumor necrosis factor-alpha (TNF-α),interleukin-6 (IL-6) and NO,in the LPS-induced the RAW 264.7 cell model (P <0.01),and inhibited the migration of neutrophils in zebrafish induced by CuSO4 (P <0.05).These results suggest that Ac-WDDCG exhibits potent anti-inflammatory activity,potentially through the inhibition of the NLRP3 signaling pathway.

Key words: Clinacanthus nutans (Burm.f.) Lindau, peptides, mitogen-activated protein kinase, Nod-like receptor family, inflammatory cytokines

中图分类号:  R285.5 TS201.2