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c-Ha-ras基因产物对组织蛋白酶L诱导的表皮生长因子受体降解的抑制作用。

Inhibition of cathepsin L-induced degradation of epidermal growth factor receptors by c-Ha-ras gene products.

作者信息

Hiwasa T, Sakiyama S, Yokoyama S, Ha J M, Fujita J, Noguchi S, Bando Y, Kominami E, Katunuma N

机构信息

Division of Biochemistry, Chiba Cancer Center Research Institute, Japan.

出版信息

Biochem Biophys Res Commun. 1988 Feb 29;151(1):78-85. doi: 10.1016/0006-291x(88)90561-x.

Abstract

The inhibitory activities of c-Ha-ras gene products (p21s) toward several cysteine proteinases have been investigated. The activity of cathepsin L was inhibited by p21s most effectively while those of cathepsin B and papain were slightly inhibited by p21s. p21s did not show any inhibitory activity toward cathepsin H. In order to connect the protease-inhibitor activity of p21s with cell growth, the degradation of epidermal growth factor receptors (EGF-receptors) was investigated. EGF-receptors were preferentially cleaved by cathepsin L but not by cathepsin B or H. The cleavage of EGF-receptors by cathepsin L was inhibited by p21s dose-dependently. These results raise the possibility that p21s can suppress the degradation of growth-related proteins such as EGF-receptors and thereby affect cell growth.

摘要

已对c-Ha-ras基因产物(p21s)对几种半胱氨酸蛋白酶的抑制活性进行了研究。组织蛋白酶L的活性被p21s最有效地抑制,而组织蛋白酶B和木瓜蛋白酶的活性则被p21s轻微抑制。p21s对组织蛋白酶H没有任何抑制活性。为了将p21s的蛋白酶抑制活性与细胞生长联系起来,研究了表皮生长因子受体(EGF受体)的降解。EGF受体优先被组织蛋白酶L切割,而不被组织蛋白酶B或H切割。p21s剂量依赖性地抑制组织蛋白酶L对EGF受体的切割。这些结果增加了p21s可以抑制诸如EGF受体等生长相关蛋白的降解从而影响细胞生长的可能性。

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