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人乳头瘤病毒16型E2蛋白中的人T辅助细胞表位与人B细胞表位及假定的细胞毒性T细胞表位重叠。

Human T helper cell epitopes overlap B cell and putative cytotoxic T cell epitopes in the E2 protein of human papillomavirus type 16.

作者信息

Lehtinen M, Hibma M H, Stellato G, Kuoppala T, Paavonen J

机构信息

Dept of Chronic Viral Diseases, National Public Health Inst, Helsinki, Finland.

出版信息

Biochem Biophys Res Commun. 1995 Apr 17;209(2):541-6. doi: 10.1006/bbrc.1995.1535.

Abstract

Activation of T helper cells is a prerequisite for the function of cytotoxic T lymphocytes (CTL) and the maturation of the B cell response. Because epitopes recognized by each of these cells may overlap, we scanned the E2 protein of human papillomavirus (HPV) type 16 to identify the T helper cell epitopes. Four major T helper cell epitopes (mapping between aa:s 11-25, 141-155, 191-205 & 231-245) and adjacent human B cell epitopes were found. The first peptide-defined epitope (RLNV) 11CQDKILTHYENDSTD25 overlapped five putative HLA-I (A1, A2, A0205, A3 & A11) binding motifs (CQDKILTHY, RLNVCQDKI, NVCQDKIL, RLNVCQDK & RLNVCQDK). This epitope is also part of an N-terminal alpha-helix which may form four HLA-II (DR2, DR4, DR7 & DR8) specific agretopes for structures recognizable by the T cell receptor (e.g. KILT). The second epitope 141EEASVTVVEGOVDYY155 (GLYY) overlapped the putative HLA-A1 & HLA-Bw37 binding motifs (VVEGQVDYY/QVDYYGLYY and EEASVTVV), and two HLA-II (DR1 & DR3) specific agretopes. The third and fourth epitopes were not associated with more than one putative CTL epitope each. Only the first epitope shared considerable aa-homology with corresponding regions of other genital HPV types.

摘要

辅助性T细胞的激活是细胞毒性T淋巴细胞(CTL)发挥功能以及B细胞反应成熟的前提条件。由于这些细胞各自识别的表位可能重叠,我们扫描了16型人乳头瘤病毒(HPV)的E2蛋白以鉴定辅助性T细胞表位。发现了四个主要的辅助性T细胞表位(定位在氨基酸11 - 25、141 - 155、191 - 205和231 - 245之间)以及相邻的人B细胞表位。第一个由肽段定义的表位(RLNV)11CQDKILTHYENDSTD25与五个推定的HLA - I(A1、A2、A0205、A3和A11)结合基序(CQDKILTHY、RLNVCQDKI、NVCQDKIL、RLNVCQDK和RLNVCQDK)重叠。该表位也是N端α螺旋的一部分,该α螺旋可能形成四个HLA - II(DR2、DR4、DR7和DR8)特异性聚集位,用于T细胞受体可识别的结构(如KILT)。第二个表位141EEASVTVVEGQVDYY155(GLYY)与推定的HLA - A1和HLA - Bw37结合基序(VVEGQVDYY/QVDYYGLYY和EEASVTVV)以及两个HLA - II(DR1和DR3)特异性聚集位重叠。第三和第四个表位各自与不超过一个推定的CTL表位相关。只有第一个表位与其他生殖道HPV类型的相应区域具有相当程度的氨基酸同源性。

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