Snijders A, Benaissa-Trouw B J, Oosting J D, Snippe H, Kraaijeveld C A
Eijkman-Winkler Laboratory of Medical Microbiology, University of Utrecht, The Netherlands.
Cell Immunol. 1989 Oct 1;123(1):23-35. doi: 10.1016/0008-8749(89)90265-7.
Mapping of T-cell epitopes on the structural proteins of Semliki Forest virus (SFV) was performed by measuring the ability of cloned SFV protein fragments to induce delayed-type hypersensitivity (DTH). The cloned SFV protein fragments were expressed as hybrid proteins with cro-beta-galactosidase in Escherichia coli from constructed recombinant plasmids. DTH reactions were measured, as footpad swelling, in BALB/c mice after immunization with whole, UV-inactivated SFV and challenge with the hybrid proteins, and vice versa, using the adjuvant dimethyl dioctadecyl ammonium bromide to enhance DTH. Only two of the tested hybrid proteins induced DTH, and these DTH reactions were equally strong. The largest DTH-inducing hybrid protein contained the N-terminal 350 amino acids of E2 and part of E3, the smallest contained only the region from amino acid residues 115 to 151 of the E2 membrane protein without any other SFV protein parts. It was concluded that the segment between amino acid residues 115 and 151 of the E2 membrane protein of SFV was responsible for the observed DTH, and thus, contains a T-cell epitope. Sequence homology with known T-cell epitopes on other proteins makes it likely that the DTH-inducing T-cell epitope is located from amino acid residues 120 to 128 of E2.
通过测量克隆的塞姆利基森林病毒(SFV)蛋白片段诱导迟发型超敏反应(DTH)的能力,对SFV结构蛋白上的T细胞表位进行了定位。从构建的重组质粒中,在大肠杆菌中将克隆的SFV蛋白片段表达为与cro-β-半乳糖苷酶的融合蛋白。在用完整的、紫外线灭活的SFV免疫并用融合蛋白攻击后,在BALB/c小鼠中测量DTH反应,以足垫肿胀表示,反之亦然,使用佐剂二甲基二十八烷基溴化铵增强DTH。所测试的融合蛋白中只有两种诱导了DTH,并且这些DTH反应同样强烈。诱导DTH最强的融合蛋白包含E2的N端350个氨基酸和E3的一部分,最小的只包含E2膜蛋白氨基酸残基115至151的区域,没有任何其他SFV蛋白部分。得出的结论是,SFV的E2膜蛋白氨基酸残基115和151之间的片段导致了观察到的DTH,因此,包含一个T细胞表位。与其他蛋白上已知T细胞表位的序列同源性表明,诱导DTH的T细胞表位可能位于E2的氨基酸残基120至128处。