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Development of a rapid one-step immunochromatographic assay for HCV core antigen detection

机译:用于HCV核心抗原检测的快速一步免疫色谱测定方法的开发

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摘要

The hepatitis C virus (HCV) core protein possesses amino acid sequences highly conserved among HCV isolates and has proved useful for various diagnostic tests. To date, no information has been published regarding the development of an immunochromatographic test for HCV core antigen detection. Therefore, the aim of this research was to develop a rapid, easily performed, highly sensitive and specific test for detection of the HCV core antigen, based on the immunochromatographic strip. The genomic region encoding the core protein (amino acids 1-136) of the hepatitis C virus was expressed in Escherichia coli as a recombinant fusion protein with glutathione S-transferase (GST) cloned into the prokaryotic expression vector pET42a and was confirmed by immunological detection with HCV positive serum. Positive reactions were detected weakly at a 1:15 dilution of the serum and more strongly in 1:10, 1:5, 1:2 and 1:1 dilutions, by the immunochromatographic test. In addition, the test was capable of detecting 0.25-12.0 mu g of the recombinant protein. This immunochromatographic technique opens new perspectives for the diagnosis of hepatitis C during the early seroconversion phase and for a rapid core antigen detection.
机译:丙型肝炎病毒(HCV)核心蛋白具有在HCV分离株中高度保守的氨基酸序列,并已证明可用于各种诊断测试。迄今为止,尚未发表有关用于HCV核心抗原检测的免疫色谱测试方法的信息。因此,本研究的目的是基于免疫色谱条,开发一种快速,易于执行,高度灵敏和特异的检测HCV核心抗原的检测方法。编码丙型肝炎病毒核心蛋白(氨基酸1-136)的基因组区域在大肠杆菌中以重组融合蛋白的形式表达,其中谷胱甘肽S转移酶(GST)被克隆到原核表达载体pET42a中,并通过免疫学检测得到证实HCV阳性血清。通过免疫色谱测试,在血清的1:15稀释度下检测到的阳性反应较弱,而在1:10、1:5、1:2和1:1的稀释度下则检测到阳性反应。另外,该测试能够检测0.25-12.0μg的重组蛋白。这种免疫色谱技术为早期血清转化阶段的丙型肝炎诊断和快速核心抗原检测开辟了新的前景。

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