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小鼠肝炎病毒核衣壳蛋白RNA结合结构域的定位

Localization of the RNA-binding domain of mouse hepatitis virus nucleocapsid protein.

作者信息

Nelson G W, Stohlman S A

机构信息

Department of Microbiology, University of Southern California School of Medicine, Los Angeles 90033.

出版信息

J Gen Virol. 1993 Sep;74 ( Pt 9):1975-9. doi: 10.1099/0022-1317-74-9-1975.

Abstract

The 454-amino acid nucleocapsid (N) protein of mouse hepatitis virus (MHV) binds the leader RNA sequence located at the 5' ends of all plus-sense genomic and subgenomic viral mRNAs. Purified N protein was cleaved with formic acid to determine which domain interacts with the leader RNA sequence. Incubation at 42 degrees C resulted in partial cleavage into two fragments of M(r)s of approximately 32K and 37K and three fragments of 17K, 16K and 14K. Incubation at 56 degrees C resulted in complete cleavage yielding only the three lower molecular mass products. Both the 32K and 37K partial cleavage products and one of the complete cleavage products bind MHV leader RNA, suggesting that the central region of the N protein contains the RNA-binding domain. Monoclonal antibody mapping of the cleavage products confirmed that the MHV leader RNA binding domain is contained within the central 140-amino acid fragment, comprising amino acids 169 to 308. Analysis of the amino acids within this domain indicates no similarity to any previously described RNA-binding protein, suggesting that N protein may possess a unique RNA-binding motif.

摘要

小鼠肝炎病毒(MHV)的454个氨基酸的核衣壳(N)蛋白与位于所有正链基因组和亚基因组病毒mRNA 5'端的前导RNA序列结合。用甲酸切割纯化的N蛋白,以确定哪个结构域与前导RNA序列相互作用。在42℃孵育导致部分切割成两个分子量约为32K和37K的片段以及三个17K、16K和14K的片段。在56℃孵育导致完全切割,仅产生三个较低分子量的产物。32K和37K的部分切割产物以及一个完全切割产物都与MHV前导RNA结合,表明N蛋白的中央区域包含RNA结合结构域。对切割产物的单克隆抗体定位证实,MHV前导RNA结合结构域包含在中央140个氨基酸的片段内,该片段由氨基酸169至308组成。对该结构域内氨基酸的分析表明,它与任何先前描述的RNA结合蛋白没有相似性,这表明N蛋白可能具有独特的RNA结合基序。

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