School of Food Science and Pharmaceutical Engineering, Nanjing Normal University, Nanjing, 210046, China; School of Life Science, Jiangsu Normal University, Xuzhou, 221116, China.
School of Food Science and Pharmaceutical Engineering, Nanjing Normal University, Nanjing, 210046, China.
Dev Comp Immunol. 2023 Oct;147:104901. doi: 10.1016/j.dci.2023.104901. Epub 2023 Jul 31.
The enzyme gamma-interferon-inducible lysosomal thiol reductase (GILT) plays an important role in promoting the processing and presentation of major histocompatibility complex (MHC) class II-restricted antigens. It is also involved in MHC I-restricted antigens catalyzing disulfide bond reduction in fishes' adaptive immunity. The open reading frame of tongue sole (Cynoglossus semilaevis) GILT (tsGILT) gene is 771 bp long, encoding 257 amino acids, with a calculated molecular weight of 28.465 kDa and isoelectric point (pI) of 5.35. After induction with lipopolysaccharide, the expression of tsGILT mRNA was upregulated in spleen and kidney and recombinant tsGILT protein transferred to late endosomes and lysosomes in HeLa cells. The refolded tsGILT was capable of catalyzing the reduction of the interchain disulfide bonds against an IgG substrate depend on the active site CXXC motif at residues 75-78. The process of immune response to bacteria challenge needs GILT to catalyze the reduction of disulfide bond and unfolding native protein antigens, promoting their hydrolysis by proteases. Whether a single mutation or a double mutation of active site CXXC at residues75-78, the 3D structure of tsGILT protein has undergone major changes and lost its activity of catalyzing the reduction of the interchain disulfide bonds.
γ-干扰素诱导的溶酶体硫醇还原酶(GILT)在促进主要组织相容性复合体(MHC)Ⅱ类限制性抗原的加工和呈递方面发挥着重要作用。它还参与鱼类适应性免疫中 MHC I 类限制性抗原催化二硫键还原。舌鳎(Cynoglossus semilaevis)GILT(tsGILT)基因的开放阅读框长 771bp,编码 257 个氨基酸,计算分子量为 28.465kDa,等电点(pI)为 5.35。用脂多糖诱导后,tsGILT mRNA 在脾脏和肾脏中的表达上调,重组 tsGILT 蛋白在 HeLa 细胞中转位到晚期内体和溶酶体。复性的 tsGILT 能够依赖于残基 75-78 处的活性位点 CXXC 基序,催化 IgG 底物中二硫键的还原。在细菌攻击的免疫反应过程中,GILT 需要催化二硫键的还原和天然蛋白抗原的展开,促进蛋白酶对其水解。无论是活性位点 CXXC 残基 75-78 处的单个突变还是双突变,tsGILT 蛋白的 3D 结构都发生了重大变化,丧失了催化二硫键还原的活性。