Mirzadeh Abolfazl, Saadatnia Geita, Golkar Majid, Babaie Jalal, Noordin Rahmah
Department of Biotechnology, Iranian Research Organization for Science and Technology (IROST), Tehran, Iran; Molecular Parasitology Laboratory, Department of Parasitology, Pasteur Institute of Iran, Tehran, Iran.
Department of Biotechnology, Iranian Research Organization for Science and Technology (IROST), Tehran, Iran.
Protein Expr Purif. 2017 May;133:66-74. doi: 10.1016/j.pep.2017.03.001. Epub 2017 Mar 2.
SAG1-related sequence 3 (SRS3) is one of the major Toxoplasma gondii tachyzoite surface antigens and has been shown to be potentially useful for the detection of toxoplasmosis. This protein is highly conformational due to the presence of six disulfide bonds. To achieve solubility and antigenicity, SRS3 depends on proper disulfide bond formation. The aim of this study was to over-express the SRS3 protein with correct folding for use in serodiagnosis of the disease. To achieve this, a truncated SRS3 fusion protein (rtSRS3) was produced, containing six histidyl residues at both terminals and purified by immobilized metal affinity chromatography. The refolding process was performed through three methods, namely dialysis in the presence of chemical additives along with reduced/oxidized glutathione and drop-wise dilution methods with reduced/oxidized glutathione or reduced DTT/oxidized glutathione. Ellman's assay and ELISA showed that the protein folding obtained by the dialysis method was the most favorable, probably due to the correct folding. Subsequently, serum samples from individuals with chronic infection (n = 76), probable acute infection (n = 14), and healthy controls (n = 81) were used to determine the usefulness of the refolded rtSRS3 for Toxoplasma serodiagnosis. The results of the developed IgG-ELISA showed a diagnostic specificity of 91% and a sensitivity of 82.89% and 100% for chronic and acute serum samples, respectively. In conclusion, correctly folded rtSRS3 has the potential to be used as a soluble antigen for the detection of human toxoplasmosis.
SAG1相关序列3(SRS3)是刚地弓形虫速殖子的主要表面抗原之一,已被证明在弓形虫病检测中具有潜在用途。由于存在六个二硫键,该蛋白具有高度的构象性。为了实现溶解性和抗原性,SRS3依赖于正确的二硫键形成。本研究的目的是过量表达具有正确折叠的SRS3蛋白,用于该疾病的血清学诊断。为此,制备了一种截短的SRS3融合蛋白(rtSRS3),其两端含有六个组氨酸残基,并通过固定化金属亲和层析进行纯化。复性过程通过三种方法进行,即在化学添加剂存在下与还原型/氧化型谷胱甘肽一起透析,以及用还原型/氧化型谷胱甘肽或还原型二硫苏糖醇/氧化型谷胱甘肽进行逐滴稀释法。Ellman检测和ELISA表明,通过透析法获得的蛋白折叠最有利,可能是由于正确的折叠。随后,使用来自慢性感染个体(n = 76)、可能的急性感染个体(n = 14)和健康对照(n = 81)的血清样本,来确定复性后的rtSRS3在弓形虫血清学诊断中的实用性。所开发的IgG-ELISA结果显示,对于慢性和急性血清样本,诊断特异性分别为91%,敏感性分别为82.89%和100%。总之,正确折叠的rtSRS3有潜力用作检测人类弓形虫病的可溶性抗原。