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首页> 外文期刊>Journal of Medical Virology >Mapping of linear antigenic determinants on glycoprotein C of herpes simplex virus type 1 and type 2 recognized by human serum immunoglobulin G antibodies.
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Mapping of linear antigenic determinants on glycoprotein C of herpes simplex virus type 1 and type 2 recognized by human serum immunoglobulin G antibodies.

机译:线性抗原决定簇在人血清免疫球蛋白G抗体识别的1型和2型单纯疱疹病毒糖蛋白C上的定位。

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Using membrane-based dekapeptides, the reactivity of human serum antibodies with linear antigenic determinants of herpes simplex virus (HSV) type 1 and type 2 glycoprotein C (gC-1, gC-2) was studied by pep scan and immunodot assay. The entire coding sequences of gC-1 and gC-2 were screened for the presence of linear epitopes by pep scan. Peptides recognized in an HSV-1 type-specific manner were mainly identified within the N-terminal third and at the C-terminus of gC-1, whereas most type-common antibodies were directed against colinear peptides within the central parts of gC-1 and gC-2. The type-specific reaction of human sera with gC-2 peptides in pep scan was poor. Eight peptides identified as immunoreactive by pep scan were further tested in immunodot assay for their reactivity with a human serum panel. None of the eight HSV-negative sera gave positive results by immunodot assay. Positive reactions with gC peptides were found to be strongly age-dependent, i.e., the rate of positive reactions was significantly higher in HSV-positive adults than in HSV-positive children. Antibody reactivity with two type-common gC peptides was demonstrated in 17 out of 28 HSV-positive sera. A putative type-specific gC-2 peptide employed in immunodot assay was inconsistently recognized by human sera. Twenty HSV-positive sera reacted with at least 1 of 5 type-specific gC-1 peptides. Nine sera showing no reactivity with glycoprotein G of HSV-1 (gG-1) by immunobloting recognized type-specific gC-1 peptides in immunodot assay. Thus, gC-1 peptides might allow the detection of HSV-1-specific antibodies in individuals showing no reactivity with commonly employed HSV-1-specific diagnostic antigenes, i.e., purified or recombinant gG-1.
机译:使用基于膜的十肽,通过pep扫描和免疫斑点测定法研究人血清抗体与1型单纯疱疹病毒(HSV)和2型糖蛋白C(gC-1,gC-2)的线性抗原决定簇的反应性。通过pep扫描筛选gC-1和gC-2的整个编码序列中线性表位的存在。以HSV-1类型特异性方式识别的肽主要在gC-1的N末端第三个和C末端鉴定,而大多数类型常见的抗体针对gC-1中心部分的共线肽和gC-2。在pep扫描中,人血清与gC-2肽的类型特异性反应差。通过pep扫描鉴定为具有免疫反应性的8种肽在immunodot分析中进一步测试了它们与人血清组的反应性。通过免疫斑点测定法,八个HSV阴性血清均未给出阳性结果。发现与gC肽的阳性反应强烈依赖于年龄,即,HSV阳性成年人的阳性反应率显着高于HSV阳性儿童。在28例HSV阳性血清中的17例中证明了与两种常见gC肽的抗体反应性。在人血清中不能一致地识别在免疫斑点测定中使用的推定的类型特异性gC-2肽。 20种HSV阳性血清与5种类型特异性gC-1肽中的至少一种反应。通过免疫斑点法在识别的类型特异性gC-1肽上免疫印迹,显示与HSV-1糖蛋白G(gG-1)无反应的九个血清。因此,gC-1肽可以允许在与通常使用的HSV-1特异性诊断抗原即纯化或重组gG-1没有反应性的个体中检测HSV-1特异性抗体。

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