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小反刍兽疫病毒核衣壳蛋白高变区T辅助细胞和线性B表位的鉴定及其在开发检测病毒抗原的特异性抗体中的应用。

Identification of T-helper and linear B epitope in the hypervariable region of nucleocapsid protein of PPRV and its use in the development of specific antibodies to detect viral antigen.

作者信息

Dechamma H J, Dighe V, Kumar C Ashok, Singh R P, Jagadish M, Kumar Satish

机构信息

Indian Veterinary Research Institute, Molecular Virology Lab, Bangalore Campus, Hebbal, Bangalore, India.

出版信息

Vet Microbiol. 2006 Dec 20;118(3-4):201-11. doi: 10.1016/j.vetmic.2006.07.023. Epub 2006 Aug 2.

Abstract

Peste des petits ruminants is a highly contagious viral disease of small ruminants making its diagnosis difficult from the similar symptoms of Rinderpest. Computer based prediction algorithms was applied to identify antigenic determinants on the nucleocapsid (N) protein of PPRV. Specificity and antigenicity of each peptide was evaluated by solid phase ELISA. Six specific peptide sequences were evaluated in multiple antigenic peptide (MAP) form and immune response was evaluated by supplementing universal T-helper epitope human IL-1beta peptide (VQGEESNDK, amino acids 163-171). Out of the six peptides 19mer sequence corresponding to 454-472 region of N protein of PPRV was found to be highly immunogenic and specific to PPRV. Evaluation of overlapping peptides differing in length for this 452-472 region, showed minimum length of 14 amino acid residues were required for the stable affinity binding of antigen-antibody. The results of immunization and indirect ELISA indicated the presence of T-helper epitope at the N-terminal end and linear B epitope at the C-terminal region of 454-472 19mer of nucleocapsid peptide of PPRV-nucleocapsid protein. The antipeptide antibodies developed against this region showed specificity to PPRV antigen differentiating it from RPV when used in indirect ELISA and western blot analysis.

摘要

小反刍兽疫是小反刍动物的一种高度传染性病毒性疾病,由于其症状与牛瘟相似,难以诊断。应用基于计算机的预测算法来鉴定小反刍兽疫病毒(PPRV)核衣壳(N)蛋白上的抗原决定簇。通过固相ELISA评估每种肽的特异性和抗原性。以多抗原肽(MAP)形式评估六个特异性肽序列,并通过补充通用T辅助表位人IL-1β肽(VQGEESNDK,氨基酸163 - 171)来评估免疫反应。在这六个肽中,发现与PPRV N蛋白454 - 472区域相对应的19聚体序列具有高度免疫原性且对PPRV具有特异性。对该452 - 472区域不同长度的重叠肽进行评估,结果表明抗原 - 抗体稳定亲和结合所需的最小长度为14个氨基酸残基。免疫和间接ELISA结果表明,在PPRV核衣壳蛋白的454 - 472 19聚体的N末端存在T辅助表位,在C末端区域存在线性B表位。针对该区域产生的抗肽抗体在间接ELISA和蛋白质印迹分析中对PPRV抗原显示出特异性,可将其与牛瘟病毒(RPV)区分开来。

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