The complete primary structure of mouse 20S proteasomes

被引:35
作者
Elenich, LA
Nandi, D
Kent, AE
McCluskey, TS
Cruz, M
Iyer, MN
Woodward, EC
Conn, CW
Ochoa, AL
Ginsburg, DB
Monaco, JJ
机构
[1] Univ Cincinnati, Howard Hughes Med Inst, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Dept Mol Genet, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Dept Cell Biol, Cincinnati, OH 45267 USA
[4] Virginia Commonwealth Univ, Dept Microbiol & Immunol, Richmond, VA 23298 USA
关键词
proteasome; antigen processing; multicatalytic proteinase; proteolysis; protein degradation;
D O I
10.1007/s002510050562
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The proteasome is a large multicatalytic proteinase that plays a role in the generation of peptides for presentation by major histocompatibility complex class I molecules. The 20S proteolytic core of mammalian proteasomes is assembled from a group of 17 protein subunits that generate a distinctive pattern of spots upon two-dimensional gel electrophoresis. The genes for most of these subunits have been cloned from humans and rats. We isolated cDNA clones for the mouse orthologues of ten of the subunits [PSMA1 (C2), PSMA2 (C3), PSMA3 (C8), PSMA4 (C9), PSMA5 (ZETA), PSMA6 (IOTA), PSMA7 (C6-I), PSMB2 (C7-I), PSMB3 (C10-II), and PSMB5 (X)] to complete the cloning of all of the mouse subunits. Using antisera raised against these subunits or their orthologues, we verified the identity of these proteins by two-dimensional NEPHGE-PAGE.
引用
收藏
页码:835 / 842
页数:8
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