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蛋白酶体亚基与主要组织相容性复合体相关LMP基因的同源性。

Homology of proteasome subunits to a major histocompatibility complex-linked LMP gene.

作者信息

Martinez C K, Monaco J J

机构信息

Department of Microbiology & Immunology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0678.

出版信息

Nature. 1991 Oct 17;353(6345):664-7. doi: 10.1038/353664a0.

Abstract

The class II region of the major histocompatibility complex (MHC) contains genes encoding at least two subunits of a large, intracellular protein complex (the low molecular mass polypeptide, or LMP, complex). This complex is biochemically similar to the proteasome, an abundant and well conserved protein complex having multiple proteolytic activities. Here we report the isolation of a complementary DNA corresponding to one of the subunits of the LMP complex, LMP-2. The protein predicted from this cDNA sequence closely matches the amino-terminal peptide sequence of a rat proteasome subunit, confirming that the proteasome and the LMP complex share polypeptide subunits. The LMP-2 gene is tightly linked to HAM1, a gene thought to be required for translocating peptide fragments of endogenous antigens into the endoplasmic reticulum for association with MHC class I molecules. These observations suggest that the LMP complex may be responsible for generating peptides from cytoplasmic antigen during antigen processing.

摘要

主要组织相容性复合体(MHC)的II类区域包含编码一种大型细胞内蛋白复合体(低分子量多肽,即LMP复合体)至少两个亚基的基因。该复合体在生化性质上与蛋白酶体相似,蛋白酶体是一种丰富且高度保守的具有多种蛋白水解活性的蛋白复合体。在此,我们报告了与LMP复合体的一个亚基LMP - 2相对应的互补DNA的分离。从该cDNA序列预测的蛋白质与大鼠蛋白酶体亚基的氨基末端肽序列紧密匹配,证实蛋白酶体和LMP复合体共享多肽亚基。LMP - 2基因与HAM1紧密连锁,HAM1是一个被认为是将内源性抗原的肽片段转运到内质网以与MHC I类分子结合所必需的基因。这些观察结果表明,LMP复合体可能在抗原加工过程中负责从细胞质抗原产生肽段。

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