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首页> 外文期刊>Scandinavian journal of immunology. >Major Histocompatibility Complex Class I-Restricted Presentation of Protein Antigens without Prior Intracellular Processing.
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Major Histocompatibility Complex Class I-Restricted Presentation of Protein Antigens without Prior Intracellular Processing.

机译:无需事先进行细胞内加工的蛋白质抗原的主要组织相容性复合体I类限制表达。

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摘要

Proteins in their native form are incapable of stimulating antigen (Ag)-specific T cells, which can only recognize major histocompatibility complex (MHC)-bound peptides that have been generated by intracellular processing within antigen-presenting cells (APCs). Here, we show that APCs can trigger MHC class I-restricted T-cell responses after presenting proteins without conventional intracellular processing, provided the immunostimulatory MHC class I-binding peptide sequence is incorporated at the carboxy-terminal position. Such MHC-bound proteins do not stimulate T cells directly, because the contact between MHC/peptide complex and its cognate ligand is sterically hindered by the amino-terminal bulk of the protein. Removal of the latter via an extracellular Ag proteolysis by the T-cell- and/or APC-derived enzymes is required for effective T-cell stimulation. Our data challenge the established concept that only small peptides can bind to the MHC class I molecules.
机译:天然形式的蛋白质无法刺激抗原(Ag)特异的T细胞,该T细胞只能识别抗原提呈细胞(APC)中通过细胞内加工产生的主要组织相容性复合物(MHC)结合肽。在这里,我们展示了APC在提供蛋白质后无需常规细胞内加工即可触发I类MHC限制的T细胞应答,前提是免疫刺激性MHC I类结合肽序列在羧基末端位置掺入。这样的MHC结合蛋白不会直接刺激T细胞,因为MHC /肽复合物与其同源配体之间的接触在空间上受到该蛋白氨基末端本体的阻碍。有效的T细胞刺激需要通过T细胞和/或APC衍生的酶通过胞外Ag蛋白水解去除后者。我们的数据挑战了只有小肽才能结合MHC I类分子的既定概念。

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