School of Chemistry and Life Sciences, Changchun University of Technology, Changchun 130012, China.
National Engineering Research Center of Edible Fungi, Ministry of Science and Technology (MOST), Key Laboratory of Edible Fungi Resources and Utilization (South), Ministry of Agriculture, Institution of Edible Fungi, Shanghai Academy of Agricultural Sciences, Shanghai 201403, China.
Molecules. 2023 Jun 15;28(12):4796. doi: 10.3390/molecules28124796.
A novel fungal immunomodulatory protein (FIP), identified as FIP-hma, was discovered in the genome of an edible mushroom . Bioinformatics analysis suggested FIP-hma contained the cerato-platanin (CP) conserved domain and was categorized into Cerato-type FIP. In phylogenetic analysis, FIP-hma was clustered into a new branch of the FIP family, displaying large system divergence from most of the other FIPs. The higher gene expression of FIP-hma was observed during the vegetative growth stages than that during the reproductive growth stages. In addition, the cDNA sequence of FIP-hma was cloned and successfully expressed in () BL21(DE3). The recombinant protein of FIP-hma (rFIP-hma) was neatly purified and isolated by Ni-NTA and SUMO-Protease. The iNOS, IL-6, IL-1β, and TNF-α levels of RAW 264.7 macrophages were upregulated by rFIP-hma, indicating its activation of an immune response by regulating central cytokines. No cytotoxic effects were observed in an MTT test. The findings of this work discovered a novel immunoregulatory protein from provided a systematic bioinformatic profile, suggested an effective approach for its heterologous recombinant production, and reported its potent immunoregulatory activity in macrophages. This study sheds light on the physiological function research of FIPs and their further industrial utilization.
从一种可食用蘑菇的基因组中发现了一种新型真菌免疫调节蛋白(FIP),鉴定为 FIP-hma。生物信息学分析表明,FIP-hma 含有角蛋白PLATANIN(CP)保守结构域,被归类为 Cerato-type FIP。在系统发育分析中,FIP-hma 聚类到 FIP 家族的一个新分支,与大多数其他 FIP 表现出较大的系统分化。在营养生长阶段,FIP-hma 的基因表达水平高于生殖生长阶段。此外,成功地克隆了 FIP-hma 的 cDNA 序列,并在 () BL21(DE3)中表达。通过 Ni-NTA 和 SUMO-Protease 对 FIP-hma 的重组蛋白(rFIP-hma)进行了整齐的纯化和分离。rFIP-hma 上调了 RAW 264.7 巨噬细胞的 iNOS、IL-6、IL-1β 和 TNF-α 水平,表明其通过调节中心细胞因子激活免疫反应。MTT 试验未观察到细胞毒性作用。这项工作的发现从 中发现了一种新型免疫调节蛋白,提供了系统的生物信息学概况,提出了一种有效的异源重组生产方法,并报道了其在巨噬细胞中的有效免疫调节活性。本研究为 FIPs 的生理功能研究及其进一步的工业利用提供了新的思路。