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脊髓灰质炎病毒聚尿苷酸聚合酶和RNA复制酶具有相同的病毒多肽。

Poliovirus polyuridylic acid polymerase and RNA replicase have the same viral polypeptide.

作者信息

Flanegan J B, Baltimore D

出版信息

J Virol. 1979 Jan;29(1):352-60. doi: 10.1128/JVI.29.1.352-360.1979.

Abstract

A poliovirus-specific polyuridylic acid [poly(U)] polymerase that copies a polyadenylic acid template complexed to an oligouridylic acid primer was isolated from the membrane fraction of infected HeLa cells and was found to sediment at 4 to 5S on a linear 5 to 20% glycerol gradient. When the poly(U) polymerase was isolated from cells labeled with [(35)S]methionine and was analyzed by glycerol gradient centrifugation and polyacrylamide gel electrophoresis, the position of only one viral protein was found to correlate with the location of enzyme activity. This protein had an apparent molecular weight of 62,500 based on its electrophoretic mobility relative to that of several molecular weight standards and was designated p63. When the poly(U) polymerase was isolated from the soluble fraction of a cytoplasmic extract, the activity was found to sediment at about 7S. In this case, however, both p63 and NCVP2 (77,000-dalton precursor of p63) cosedimented with the 7S activity peak. When the 7S polymerase activity was purified by phosphocellulose chromatography, both p63 and NCVP2 were found to co-chromatograph with poly(U) polymerase activity. The poliovirus replicase complexed with its endogenous RNA template was isolated from infected cells labeled with [(35)S]methionine and was centrifuged through a linear 15 to 30% glycerol gradient. The major viral polypeptide component in a 26S peak of replicase activity was p63, but small amounts of other poliovirus proteins were also present. When the replicase-template complex was treated with RNase T1 before centrifugation, a single peak of activity was found that sedimented at 20S and contained only labeled p63. Thus, p63 was found to be the only viral polypeptide in the replicase bound to its endogenous RNA template, and appears to be active as a poly(U) polymerase either as a monomer protein or as a 7S complex.

摘要

从感染的HeLa细胞的膜部分分离出一种脊髓灰质炎病毒特异性多聚尿苷酸[poly(U)]聚合酶,它能复制与寡聚尿苷酸引物复合的多聚腺苷酸模板,并且发现在线性5%至20%甘油梯度上以4至5S沉降。当从用[(35)S]甲硫氨酸标记的细胞中分离出该多聚(U)聚合酶,并通过甘油梯度离心和聚丙烯酰胺凝胶电泳进行分析时,发现只有一种病毒蛋白的位置与酶活性的位置相关。根据其相对于几种分子量标准物的电泳迁移率,该蛋白的表观分子量为62,500,被命名为p63。当从细胞质提取物的可溶部分分离出多聚(U)聚合酶时,发现该活性以约7S沉降。然而,在这种情况下,p63和NCVP2(p63的77,000道尔顿前体)都与7S活性峰共沉降。当通过磷酸纤维素色谱法纯化7S聚合酶活性时,发现p63和NCVP2都与多聚(U)聚合酶活性共色谱。从用[(35)S]甲硫氨酸标记的感染细胞中分离出与其内源性RNA模板复合的脊髓灰质炎病毒复制酶,并通过线性15%至30%甘油梯度离心。复制酶活性的26S峰中的主要病毒多肽成分是p63,但也存在少量其他脊髓灰质炎病毒蛋白。当在离心前用RNase T1处理复制酶 - 模板复合物时,发现一个单一的活性峰以20S沉降,并且只含有标记的p63。因此,发现p63是与其内源性RNA模板结合的复制酶中唯一的病毒多肽,并且似乎作为单体蛋白或作为7S复合物作为多聚(U)聚合酶具有活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca8f/353130/0436e9dc61b1/jvirol00181-0373-a.jpg

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