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从花生条纹病毒的一个斑驳分离株中克隆衣壳蛋白基因。

Cloning of the capsid protein gene from a blotch isolate of peanut stripe virus.

作者信息

Cassidy B, Sherwood J L, Nelson R S

机构信息

Plant Biology Division, Samuel Roberts Noble Foundation, Ardmore, Oklahoma.

出版信息

Arch Virol. 1993;128(3-4):287-97. doi: 10.1007/BF01309440.

Abstract

The 3' terminal 1,367 nucleotides (nts) of a blotch isolate of the potyvirus, peanut stripe virus (PStV), were cloned and sequenced. This region included the 861 nts (287 amino acids) of the PStV capsid protein (CP). The amino acid sequence of the predicted proteinase cleavage site was identified. This region shared limited homology with other potyvirus proteinase cleavage sites. The viral CP gene sequence was followed by 254 nucleotides of 3' nontranslated sequence and a poly-A tail. Based on computer modeling, the 3' nontranslated region could form two lengthy stem-loop structures and two pseudoknot structures. Subclones containing the coding sequences of the CP (amino acids 1-287, 17-287, 17-113 and 106-287) were constructed and expressed in Escherichia coli. These polypeptides were detected using polyclonal antibodies in Western blots.

摘要

对马铃薯Y病毒属的花生条纹病毒(PStV)斑点分离株的3'末端1367个核苷酸(nts)进行了克隆和测序。该区域包括PStV衣壳蛋白(CP)的861个核苷酸(287个氨基酸)。确定了预测的蛋白酶切割位点的氨基酸序列。该区域与其他马铃薯Y病毒蛋白酶切割位点的同源性有限。病毒CP基因序列后面是254个核苷酸的3'非翻译序列和一个聚腺苷酸尾。基于计算机建模,3'非翻译区可形成两个长茎环结构和两个假结结构。构建了包含CP编码序列(氨基酸1 - 287、17 - 287、17 - 113和106 - 287)的亚克隆,并在大肠杆菌中表达。使用多克隆抗体在蛋白质免疫印迹中检测到了这些多肽。

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