Characterization of a new fungal immunomodulatory protein, FIP-dsq2 from Dichomitus squalens

被引:15
|
作者
Li, Shuying [1 ]
Jiang, Zhonghao [1 ]
Sun, Lichao [1 ]
Liu, Xin [1 ]
Huang, Ying [1 ]
Wang, Fengzhong [1 ]
Xin, Fengjiao [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Food Sci & Technol, 2 Yuan Ming Yuan W Rd, Beijing 100193, Peoples R China
关键词
Fungal immunomodulatory protein; NSCLC; Proliferation; Apoptosis; Migration; LUNG-CANCER CELLS; GANODERMA-TSUGAE; FIP-FVE; FUNCTIONAL-CHARACTERIZATION; RECOMBINANT EXPRESSION; FLAMMULINA-VELUTIPES; MUSHROOM; DEATH; PROLIFERATION; INHIBITION;
D O I
10.1016/j.jbiotec.2017.02.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
FIP-dsq2, a new immunomodulatory protein, was identified in Basidiomycota Dichomitus squalens by gene mining. FIP-dsq2 contained 111 amino acids with a molecular weight of 12.51 kDa. FIP-dsq2 had a homology range of 51-65% to the reported FIPs. The predicted 3-dimensional model had more similar identical folding patterns in LZ-8 than for FIP-fve. Evolutionary analysis indicated substantial phylogenetic differences were existed with the other FIPs. Overexpression of a 14.07 kDa soluble recombinant FIP-dsq2 (rFIP-dsq2) was achieved in Rosetta (pGEX-6P-1) and the purified recombinant protein was homodimer verified by gel filtration chromatography analysis. Antitumour ability of rFIP-dsq2 to human lung adenocarcinoma A549 cells was between LZ-8 and FIP-fve. The cytotoxic effect of rFIP-dsq2 in A549 cancer cells was dose-dependent and the half-maximal inhibitory concentration (IC50) was 15.08 mu g/mL. Furthermore, rFIP-dsq2 at 8 mu g/mL could significantly induce apoptosis and interrupt migration in A549 cells. In addition, the antitumour-mechanism exploration suggested that rFIP-dsq2 inhibited A549 proliferation uniquely via apoptotic cell death pathway. The results stated that rFIP-dsq2 was a promising candidate for use in future lung cancer therapy. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 51
页数:7
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