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三肽基肽酶I,即晚发性婴儿神经元蜡样脂褐质沉积症基因产物,启动ATP合酶亚基c的溶酶体降解。

Tripeptidyl peptidase I, the late infantile neuronal ceroid lipofuscinosis gene product, initiates the lysosomal degradation of subunit c of ATP synthase.

作者信息

Ezaki J, Takeda-Ezaki M, Kominami E

机构信息

Department of Biochemistry, Juntendo University School of Medicine, Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.

出版信息

J Biochem. 2000 Sep;128(3):509-16. doi: 10.1093/oxfordjournals.jbchem.a022781.

Abstract

The specific accumulation of a hydrophobic protein, subunit c of ATP synthase, in lysosomes from the cells of patients with the late infantile form of NCL (LINCL) is caused by a defect in the CLN2 gene product, tripeptidyl peptidase I (TPP-I). The data here show that TPP-I is involved in the initial degradation of subunit c in lysosomes and suggest that its absence leads directly to the lysosomal accumulation of subunit c. The inclusion of a specific inhibitor of TPP-I, Ala-Ala-Phe-chloromethylketone (AAF-CMK), in the culture medium of normal fibroblasts induced the lysosomal accumulation of subunit c. In an in vitro incubation experiment the addition of AAF-CMK to mitochondrial-lysosomal fractions from normal cells inhibited the proteolysis of subunit c, but not the b-subunit of ATP synthase. The use of two antibodies that recognize the aminoterminal and the middle portion of subunit c revealed that the subunit underwent aminoterminal proteolysis, when TPP-I, purified from rat spleen, was added to the mitochondrial fractions. The addition of both purified TPP-I and the soluble lysosomal fractions, which contain various proteinases, to the mitochondrial fractions resulted in rapid degradation of the entire molecule of subunit c, whereas the degradation of subunit c was markedly delayed through the specific inhibition of TPP-I in lysosomal extracts by AAF-CMK. The stable subunit c in the mitochondrial-lysosomal fractions from cells of a patient with LINCL was degraded on incubation with purified TPP-I. The presence of TPP-I led to the sequential cleavage of tripeptides from the N-terminus of the peptide corresponding to the amino terminal sequence of subunit c.

摘要

在晚发性婴儿型神经元蜡样脂褐质沉积病(LINCL)患者细胞的溶酶体中,疏水蛋白ATP合酶亚基c的特异性积累是由CLN2基因产物三肽基肽酶I(TPP-I)缺陷引起的。本文数据表明,TPP-I参与溶酶体中亚基c的初始降解,并且其缺失直接导致亚基c在溶酶体中积累。在正常成纤维细胞的培养基中加入TPP-I的特异性抑制剂丙氨酸-丙氨酸-苯丙氨酸-氯甲基酮(AAF-CMK),可诱导亚基c在溶酶体中积累。在体外孵育实验中,向正常细胞的线粒体-溶酶体组分中添加AAF-CMK可抑制亚基c的蛋白水解,但不影响ATP合酶的b亚基。使用两种识别亚基c氨基末端和中间部分的抗体发现,当将从大鼠脾脏纯化的TPP-I添加到线粒体组分中时,该亚基发生了氨基末端蛋白水解。将纯化的TPP-I和含有各种蛋白酶的可溶性溶酶体组分都添加到线粒体组分中,导致亚基c的整个分子迅速降解,而通过AAF-CMK特异性抑制溶酶体提取物中的TPP-I,亚基c的降解则明显延迟。LINCL患者细胞的线粒体-溶酶体组分中稳定的亚基c在与纯化的TPP-I孵育时会被降解。TPP-I的存在导致从与亚基c氨基末端序列相对应的肽的N末端依次切割三肽。

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