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N3的加工过程,一种哺乳动物蛋白酶体β型亚基。

Processing of N3, a mammalian proteasome beta-type subunit.

作者信息

Thomson S, Rivett A J

机构信息

Department of Biochemistry, University of Leicester, U.K.

出版信息

Biochem J. 1996 May 1;315 ( Pt 3)(Pt 3):733-8. doi: 10.1042/bj3150733.

Abstract

Proteasome subunits are encoded by members of the same gene family and can be divided into two groups based on their similarity to the alpha and beta subunits of the simpler proteasome isolated from Thermoplasma acidophilum. RN3 is the beta-type subunit, N3, of rat proteasomes which has been implicated in the peptidylglutamyl-peptide hydrolase activity of the proteinase complex. We have expressed recombinant RN3 protein in Escherichia coli in order to raise subunit-specific polyclonal antibodies. Identification of the position of RN3 on two-dimensional PAGE gels of purified rat liver proteasomes showed a single protein spot of molecular mass 24 kDa and of pI value of about 5. This protein has a free N-terminus, having undergone post-translational processing. After immunoprecipitation from [35S]methionine-labelled human embryo lung L-132 cells using anti-RN3 antibodies, two radiolabelled spots were observed on two-dimensional PAGE gels, one corresponding to the mature N3, the other of molecular mass 28.5 kDa and pI value around 5, which was probably the unprocessed form of N3. However, the latter protein had a higher molecular mass (31 kDa) than was predicted from the sequence of previously cloned cDNA. Therefore rapid amplification of cDNA ends ("RACE') was carried out to determine the full sequence. The lack of detectable RN3 precursor in purified rat liver proteasomes suggests that the processing probably accompanies assembly of the complex. The half-life of the processing was determined to be 31 min in growing L-132 cells. The unprocessed form of N3 was not observed after immunoprecipitation of 35S-labelled complexes with anti-proteasome antibodies. There was no evidence to suggest that unprocessed N3 is found in precursor complexes which have been implicated in the assembly of some other unprocessed beta-type subunits. Interestingly also, the site of cleavage of N3 (ITR decreases TQN) differs significantly from those of other processed animal beta-type proteasome subunits [(H/T)G decreases TT(T/L)], many of which resemble more closely the cleavage site of the Thermoplasma acidophilum beta subunit.

摘要

蛋白酶体亚基由同一基因家族的成员编码,根据它们与从嗜热栖热菌中分离出的较简单蛋白酶体的α和β亚基的相似性可分为两组。RN3是大鼠蛋白酶体的β型亚基N3,它与蛋白酶复合体的肽基谷氨酰肽水解酶活性有关。我们在大肠杆菌中表达了重组RN3蛋白,以制备亚基特异性多克隆抗体。在纯化的大鼠肝脏蛋白酶体的二维聚丙烯酰胺凝胶电泳(PAGE)上鉴定RN3的位置,显示出一个分子量为24 kDa、等电点约为5的单一蛋白斑点。该蛋白有一个游离的N端,经过了翻译后加工。用抗RN3抗体从[35S]甲硫氨酸标记的人胚肺L-132细胞中进行免疫沉淀后,在二维PAGE凝胶上观察到两个放射性标记斑点,一个对应成熟的N3,另一个分子量为28.5 kDa,等电点约为5,可能是N3的未加工形式。然而,后一种蛋白的分子量(31 kDa)比根据先前克隆的cDNA序列预测的要高。因此,进行了cDNA末端快速扩增(“RACE”)以确定完整序列。在纯化的大鼠肝脏蛋白酶体中未检测到可检测到的RN3前体,这表明加工可能伴随着复合体的组装。在生长的L-132细胞中,加工的半衰期被确定为31分钟。用抗蛋白酶体抗体对35S标记的复合体进行免疫沉淀后,未观察到N3的未加工形式。没有证据表明在与其他一些未加工的β型亚基组装有关的前体复合体中发现未加工的N3。有趣的是,N3的切割位点(ITR减少TQN)与其他加工后的动物β型蛋白酶体亚基的切割位点[(H/T)G减少TT(T/L)]有显著差异,其中许多与嗜热栖热菌β亚基的切割位点更相似。

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