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黑色素瘤-a/MART-1癌蛋白抗原性的计算性肽段剖析

Computational peptide dissection of Melan-a/MART-1 oncoprotein antigenicity.

作者信息

Tiwari Raj, Geliebter Jan, Lucchese Alberta, Mittelman Abraham, Kanduc Darja

机构信息

Department of Microbiology and Immunology, New York Medical College, Valhalla, NY 10595, USA.

出版信息

Peptides. 2004 Nov;25(11):1865-71. doi: 10.1016/j.peptides.2004.07.004.

Abstract

We have mapped the linear antigenic determinant of a commercial MAb raised in the mouse against the melanoma-associated-antigen Melan-A/MART-1. The B cell epitope on the Melan-A/MART-1 oncoprotein is located in the 15-mer amino acid sequence 101-115 PPAYEKLSAEQSPPP, within residues 102-106. The definition of the antigenic sequence on Melan-A/MART-1 oncoprotein was reached following analyses of MHC II binding potential and similarity level to the mouse proteome, that put into evidence the 15-mer amino acid sequence 101-115 PPAYEKLSAEQSPPP as the top scoring peptide in binding H2-A(d) molecules and the epitopic sequence residues 102-106 (i.e., the peptide sequence PAYEK) as having low-similarity level to the mouse proteome. Dot-blot epitope mapping immunoassay identified proline residue 102 as critical, based on its effect on antibody recognition. The present study adds to previous companion reports in validating the hypothesis that low-similarity to the host's proteome and binding potential to MHC II molecules are essential concurring factors in the modulation of the pool of epitopic sequences.

摘要

我们已绘制出一种在小鼠体内产生的针对黑色素瘤相关抗原Melan-A/MART-1的商用单克隆抗体的线性抗原决定簇。Melan-A/MART-1癌蛋白上的B细胞表位位于15个氨基酸序列101 - 115 PPAYEKLSAEQSPPP中,在第102 - 106位残基范围内。在对MHC II结合潜力以及与小鼠蛋白质组的相似性水平进行分析之后,确定了Melan-A/MART-1癌蛋白上的抗原序列,这表明15个氨基酸序列101 - 115 PPAYEKLSAEQSPPP是结合H2-A(d)分子得分最高的肽段,且表位序列残基102 - 106(即肽段序列PAYEK)与小鼠蛋白质组的相似性水平较低。基于脯氨酸残基102对抗体识别的影响,斑点印迹表位作图免疫测定确定其为关键残基。本研究补充了之前的相关报道,验证了以下假说:与宿主蛋白质组的低相似性以及与MHC II分子的结合潜力是调节表位序列库的重要协同因素。

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