首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >ACTIVATED DROSOPHILA RAS1 IS SELECTIVELY SUPPRESSED BY ISOPRENYL TRANSFERASE INHIBITORS
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ACTIVATED DROSOPHILA RAS1 IS SELECTIVELY SUPPRESSED BY ISOPRENYL TRANSFERASE INHIBITORS

机译:异戊基转移酶抑制剂选择性抑制活性果蝇RAS1

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摘要

Ras CAAX (C = cysteine, A = aliphatic amino acid, and X = any amino acid) peptidomimetic inhibitors of farnesyl protein transferase suppress Ras-dependent cell transformation by preventing farnesylation of the Ras oncoprotein. These compounds are potential anticancer agents for tumors associated with Ras mutations. The peptidomimetic FTI-254 was tested for Ras1-inhibiting activity in whole animals by injection of activated Ras1(val12) Drosophila larvae. FTI-254 decreased the ability of Ras1(val12) to form supernumerary R7 photoreceptor cells in the compound eye of transformed flies. In contrast, it had no effect on the related supernumerary R7 phenotypes of flies transformed with either the activated sevenless receptor tyrosine kinase, Raf kinase, or a chimeric Ras1(val12) protein that is membrane associated through myristylation instead of isoprenylation. Therefore, FTI-254 acts as an isoprenylation inhibitor to selectively inhibit Ras1(val12) signaling activity in a whole-animal model system. [References: 38]
机译:法呢基蛋白转移酶的拟肽抑制剂Ras CAAX(C =半胱氨酸,A =脂肪族氨基酸,X =任何氨基酸)通过防止Ras癌蛋白的法呢基化来抑制Ras依赖的细胞转化。这些化合物是用于与Ras突变相关的肿瘤的潜在抗癌药。通过注射活化的Ras1(val12)果蝇幼虫,对拟肽FTI-254在整个动物中的Ras1抑制活性进行了测试。 FTI-254降低了Ras1(val12)在转化果蝇的复眼中形成多余的R7感光细胞的能力。相比之下,它对用活化的七种受体酪氨酸激酶,Raf激酶或嵌合的Ras1(val12)蛋白(通过肉豆蔻酰化而不是异戊二烯化作用与膜结合)转化的果蝇的相关R7表型没有影响。因此,FTI-254充当异戊二烯化抑制剂,以选择性抑制整个动物模型系统中的Ras1(val12)信号传导活性。 [参考:38]

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