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鸡核黄素载体蛋白四种主要抗原肽中T辅助位点的表位作图及特异性评估(远交系大鼠)

Epitope mapping and evaluation of specificity of T-helper sites in four major antigenic peptides of chicken riboflavin carrier protein in outbred rats.

作者信息

Subramanian Sarada, Andal S, Karande Anjali A, Radhakantha Adiga P

机构信息

Department of Neurochemistry, National Institute of Mental Health and Neurosciences, Bangalore, India.

出版信息

Biochem Biophys Res Commun. 2003 Nov 7;311(1):11-6. doi: 10.1016/j.bbrc.2003.09.162.

Abstract

This paper reviews our studies on synthetic peptides spanning the major antigenic determinants of the chicken riboflavin carrier protein (RCP; 219 AA). These determinants are composed of residues 4-24 (YGC), 64-83 (CED), 130-147 (GEN), and 200-219 (HAC) and function as minivaccines in terms of eliciting anti-peptide antibodies which recognize the native protein and are particularly promising contraceptive vaccine candidates. We have used 15-residue synthetic peptides to define short sequences involved in interaction with antibody and with T-cells. We have mapped the boundaries of T-cell epitopes of these peptides in outbred rats by immunizing the animals with each peptide and assaying the popliteal lymph node cell proliferation against a series of overlapping synthetic 15-mers covering the entire length of the individual peptides. The peptides YGC, GEN, and HAC harboured a single T-cell epitope each whereas the peptide CED exhibited bimodal response possessing two epitopes, one at N-terminus and the other at the C-terminus. These studies provide insight into the way in which an immunogen is viewed by the immune system. In addition, preferential T-cell helper function for B cells recognizing unique determinants on the same molecule was demonstrated. This information helps in exploiting synthetic peptides in the construction of designer immunogens which have potential as candidate vaccines.

摘要

本文综述了我们对跨越鸡核黄素载体蛋白(RCP;219个氨基酸)主要抗原决定簇的合成肽的研究。这些决定簇由4 - 24位残基(YGC)、64 - 83位残基(CED)、130 - 147位残基(GEN)和200 - 219位残基(HAC)组成,在引发识别天然蛋白的抗肽抗体方面发挥微型疫苗的作用,是特别有前景的避孕疫苗候选物。我们使用15个残基的合成肽来确定与抗体和T细胞相互作用所涉及的短序列。我们通过用每种肽免疫远交系大鼠,并检测针对覆盖各个肽全长的一系列重叠合成15聚体的腘淋巴结细胞增殖,绘制了这些肽在远交系大鼠中的T细胞表位边界。肽YGC、GEN和HAC各自含有一个T细胞表位,而肽CED表现出双峰反应,拥有两个表位,一个在N端,另一个在C端。这些研究为免疫系统看待免疫原的方式提供了见解。此外,还证明了对识别同一分子上独特决定簇的B细胞具有优先T细胞辅助功能。这些信息有助于在构建具有作为候选疫苗潜力的定制免疫原时利用合成肽。

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