Wyckoff E E, Lloyd R E, Ehrenfeld E
Department of Cellular, Viral, and Molecular Biology, University of Utah School of Medicine, Salt Lake City 84132.
J Virol. 1992 May;66(5):2943-51. doi: 10.1128/JVI.66.5.2943-2951.1992.
The cleavage of the p220 subunit of eukaryotic initiation factor 4F (eIF-4F) that is induced by the poliovirus protease 2A has been shown previously to require another translation initiation factor, eIF-3. The role of eIF-3 in this cleavage reaction, however, is not known. An antiserum was raised against human eIF-3 and used to analyze the eIF-3 subunit composition in poliovirus-infected and uninfected HeLa cells and after incubation of eIF-3 in vitro with viral 2A protease. No evidence for 2Apro-dependent cleavage of any eIF-3 subunit was detected. Infected cells contain an activity that catalyzes the cleavage of p220 to a specific set of cleavage products. This activity is thought to be an activated form of a latent cellular protease. The p220-specific cleavage activity was partially purified. It was resolved from eIF-3 by both gel filtration and anion-exchange chromatography. Neither intact eIF-3 nor any detectable subunits of eIF-3 were found to copurify with the p220-specific cleavage activity. The latter activity behaves as a protein of 55,000 to 60,000 molecular weight and is inhibited by alkylating agents and metals, which indicates the presence of essential thiol groups. When this activity was incubated with partially purified p220, cleavage occurred only in the presence of eIF-3. Thus, eIF-3 appears to play a role in the p220 cleavage cascade which is subsequent to the 2Apro-induced activation of the p220-specific protease.
脊髓灰质炎病毒蛋白酶2A诱导的真核起始因子4F(eIF-4F)的p220亚基裂解,先前已表明需要另一种翻译起始因子eIF-3。然而,eIF-3在这种裂解反应中的作用尚不清楚。制备了针对人eIF-3的抗血清,并用于分析脊髓灰质炎病毒感染和未感染的HeLa细胞中的eIF-3亚基组成,以及eIF-3在体外与病毒2A蛋白酶孵育后的情况。未检测到任何eIF-3亚基发生2A蛋白酶依赖性裂解的证据。感染的细胞含有一种催化p220裂解为特定一组裂解产物的活性。这种活性被认为是一种潜在细胞蛋白酶的活化形式。对p220特异性裂解活性进行了部分纯化。通过凝胶过滤和阴离子交换色谱将其与eIF-3分离。未发现完整的eIF-3或任何可检测到的eIF-3亚基与p220特异性裂解活性共纯化。后者的活性表现为分子量为55,000至60,000的蛋白质,并受到烷基化剂和金属的抑制,这表明存在必需的巯基。当这种活性与部分纯化的p220一起孵育时,只有在eIF-3存在的情况下才会发生裂解。因此,eIF-3似乎在2A蛋白酶诱导的p220特异性蛋白酶激活之后的p220裂解级联反应中发挥作用。