Vigneron Nathalie, Stroobant Vincent, Chapiro Jacques, Ooms Annie, Degiovanni Gérard, Morel Sandra, van der Bruggen Pierre, Boon Thierry, Van den Eynde Benoît J
Ludwig Institute for Cancer Research and Cellular Genetics Unit, Université de Louvain, B-1200 Brussels, Belgium.
Science. 2004 Apr 23;304(5670):587-90. doi: 10.1126/science.1095522. Epub 2004 Mar 4.
CD8 T lymphocytes recognize peptides of 8 to 10 amino acids presented by class I molecules of the major histocompatibility complex. Here, CD8 T lymphocytes were found to recognize a nonameric peptide on melanoma cells that comprises two noncontiguous segments of melanocytic glycoprotein gp100(PMEL17). The production of this peptide involves the excision of four amino acids and splicing of the fragments. This process was reproduced in vitro by incubating a precursor peptide of 13 amino acids with highly purified proteasomes. Splicing appears to occur by transpeptidation involving an acyl-enzyme intermediate. Our results reveal an unanticipated aspect of the proteasome function of producing antigenic peptides.
CD8 T淋巴细胞识别由主要组织相容性复合体I类分子呈递的8至10个氨基酸的肽段。在此,发现CD8 T淋巴细胞识别黑色素瘤细胞上的一种九聚体肽,该肽由黑素细胞糖蛋白gp100(PMEL17)的两个不连续片段组成。这种肽的产生涉及四个氨基酸的切除和片段的拼接。通过将一个13个氨基酸的前体肽与高度纯化的蛋白酶体一起孵育,此过程在体外得以重现。拼接似乎通过涉及酰基 - 酶中间体的转肽作用发生。我们的结果揭示了蛋白酶体产生抗原肽功能中一个意想不到的方面。